Samples
General
Populations
no ancestry information available
PGS000001
Reference score
- Variants: 77
- Variants ignored: 0
-
Trait: Breast Cancer
- Mapped Trait(s):
- Samples: 22,627
- Population:
- Publication: Mavaddat N et.al, J Natl Cancer Inst (2015-04-08)
- View in PGS-Catalog
Target study
- Coverage: 74 (96.1%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000002
Reference score
- Variants: 77
- Variants ignored: 0
-
Trait: ER-positive Breast Cancer
- Mapped Trait(s):
- Samples: 22,627
- Population:
- Publication: Mavaddat N et.al, J Natl Cancer Inst (2015-04-08)
- View in PGS-Catalog
Target study
- Coverage: 74 (96.1%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000003
Reference score
- Variants: 77
- Variants ignored: 0
-
Trait: ER-negative Breast Cancer
- Mapped Trait(s):
- Samples: 22,627
- Population:
- Publication: Mavaddat N et.al, J Natl Cancer Inst (2015-04-08)
- View in PGS-Catalog
Target study
- Coverage: 74 (96.1%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000004
Reference score
- Variants: 313
- Variants ignored: 0
-
Trait: Breast Cancer
- Mapped Trait(s):
- Samples: 158,648
- Population:
- Publication: Mavaddat N et.al, Am J Hum Genet (2018-12-13)
- View in PGS-Catalog
Target study
- Coverage: 313 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000005
Reference score
- Variants: 313
- Variants ignored: 0
-
Trait: ER-positive Breast Cancer
- Mapped Trait(s):
- Samples: 87,368
- Population:
- Publication: Mavaddat N et.al, Am J Hum Genet (2018-12-13)
- View in PGS-Catalog
Target study
- Coverage: 313 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000006
Reference score
- Variants: 313
- Variants ignored: 0
-
Trait: ER-negative Breast Cancer
- Mapped Trait(s):
- Samples: 87,368
- Population:
- Publication: Mavaddat N et.al, Am J Hum Genet (2018-12-13)
- View in PGS-Catalog
Target study
- Coverage: 313 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000007
Reference score
- Variants: 3,820
- Variants ignored: 0
-
Trait: Breast Cancer
- Mapped Trait(s):
- Samples: 158,648
- Population:
- Publication: Mavaddat N et.al, Am J Hum Genet (2018-12-13)
- View in PGS-Catalog
Target study
- Coverage: 3,819 (99.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000008
Reference score
- Variants: 3,820
- Variants ignored: 0
-
Trait: ER-positive Breast Cancer
- Mapped Trait(s):
- Samples: 87,368
- Population:
- Publication: Mavaddat N et.al, Am J Hum Genet (2018-12-13)
- View in PGS-Catalog
Target study
- Coverage: 3,819 (99.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000009
Reference score
- Variants: 3,820
- Variants ignored: 0
-
Trait: ER-negative Breast Cancer
- Mapped Trait(s):
- Samples: 87,368
- Population:
- Publication: Mavaddat N et.al, Am J Hum Genet (2018-12-13)
- View in PGS-Catalog
Target study
- Coverage: 3,819 (99.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000010
Reference score
- Variants: 27
- Variants ignored: 4
-
Trait: Coronary heart disease
- Mapped Trait(s):
- Samples: 86,995
- Population:
- Publication: Mega JL et.al, Lancet (2015-03-04)
- View in PGS-Catalog
Target study
- Coverage: 21 (77.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000011
Reference score
- Variants: 50
- Variants ignored: 0
-
Trait: Coronary artery disease
- Mapped Trait(s):
- Samples: 365,042
- Population:
- Multi-Ancestry (including Europeans): 53.3%
- European: 40.3%
- South Asian: 6.4%
- Publication: Tada H et.al, Eur Heart J (2015-09-20)
- View in PGS-Catalog
Target study
- Coverage: 48 (96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000012
Reference score
- Variants: 49,310
- Variants ignored: 9,681
-
Trait: Coronary artery disease
- Mapped Trait(s):
- Samples: 194,427
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Abraham G et.al, Eur Heart J (2016-09-21)
- View in PGS-Catalog
Target study
- Coverage: 38,823 (78.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000013
Reference score
- Variants: 6,630,150
- Variants ignored: 0
-
Trait: Coronary artery disease
- Mapped Trait(s):
- Samples: 187,599
- Population:
- European: 75.3%
- South Asian: 13.6%
- East Asian: 6%
- Hispanic or Latin American: 2.2%
- African: 1.7%
- Greater Middle Eastern: 1.2%
- Publication: Khera AV et.al, Nat Genet (2018-08-13)
- View in PGS-Catalog
Target study
- Coverage: 6,630,150 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000014
Reference score
- Variants: 6,917,436
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 318,416
- Population:
- Publication: Khera AV et.al, Nat Genet (2018-08-13)
- View in PGS-Catalog
Target study
- Coverage: 6,917,436 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000015
Reference score
- Variants: 5,218
- Variants ignored: 0
-
Trait: Breast cancer
- Mapped Trait(s):
- Samples: 139,274
- Population:
- Publication: Khera AV et.al, Nat Genet (2018-08-13)
- View in PGS-Catalog
Target study
- Coverage: 5,218 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000016
Reference score
- Variants: 6,730,541
- Variants ignored: 0
-
Trait: Atrial fibrillation
- Mapped Trait(s):
- Samples: 132,118
- Population:
- European: 89.9%
- African: 4.4%
- East Asian: 3.1%
- Hispanic or Latin American: 2.5%
- Publication: Khera AV et.al, Nat Genet (2018-08-13)
- View in PGS-Catalog
Target study
- Coverage: 6,730,541 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000017
Reference score
- Variants: 6,907,112
- Variants ignored: 0
-
Trait: Inflammatory bowel disease
- Mapped Trait(s):
- Samples: 34,652
- Population:
- Publication: Khera AV et.al, Nat Genet (2018-08-13)
- View in PGS-Catalog
Target study
- Coverage: 6,907,112 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000018
Reference score
- Variants: 1,745,179
- Variants ignored: 0
-
Trait: Coronary artery disease
- Mapped Trait(s):
- Samples: 382,026
- Population:
- Multi-Ancestry (including Europeans): 50.9%
- European: 37%
- South Asian: 6.7%
- East Asian: 3%
- Hispanic or Latin American: 1.1%
- African: 0.8%
- Greater Middle Eastern: 0.6%
- Publication: Inouye M et.al, J Am Coll Cardiol (2018-10-01)
- View in PGS-Catalog
Target study
- Coverage: 1,738,276 (99.6%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000023
Reference score
- Variants: 7
- Variants ignored: 0
-
Trait: Type 1 diabetes
- Mapped Trait(s):
- Samples: 3,949
- Population:
- Publication: Onengut-Gumuscu S et.al, Diabetes Care (2019-01-18)
- View in PGS-Catalog
Target study
- Coverage: 7 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000025
Reference score
- Variants: 19
- Variants ignored: 0
-
Trait: Alzheimer's Disease
- Mapped Trait(s):
- Samples: 55,134
- Population:
- Publication: Chouraki V et.al, J Alzheimers Dis (2016-06-01)
- View in PGS-Catalog
Target study
- Coverage: 19 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000026
Reference score
- Variants: 33
- Variants ignored: 6
-
Trait: Alzheimer’s Disease
- Mapped Trait(s):
- Samples: 54,162
- Population:
- Publication: Desikan RS et.al, PLoS Med (2017-03-21)
- View in PGS-Catalog
Target study
- Coverage: 31 (93.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000027
Reference score
- Variants: 2,100,302
- Variants ignored: 0
-
Trait: Body Mass Index
- Mapped Trait(s):
- Samples: 238,944
- Population:
- European: 99.1%
- Hispanic or Latin American: 0.5%
- African: 0.4%
- Publication: Khera AV et.al, Cell (2019-04-01)
- View in PGS-Catalog
Target study
- Coverage: 2,100,302 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000028
Reference score
- Variants: 86
- Variants ignored: 0
-
Trait: Breast cancer
- Mapped Trait(s):
- Samples: 144,871
- Population:
- European: 80.7%
- East Asian: 13.4%
- Hispanic or Latin American: 3.3%
- African: 2.6%
- Publication: Shieh Y et.al, Breast Cancer Res Treat (2016-08-26)
- View in PGS-Catalog
Target study
- Coverage: 83 (96.51%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000029
Reference score
- Variants: 76
- Variants ignored: 0
-
Trait: Breast cancer
- Mapped Trait(s):
- Samples: 59,199
- Population:
- Publication: Shieh Y et.al, Breast Cancer Res Treat (2016-08-26)
- View in PGS-Catalog
Target study
- Coverage: 76 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000030
Reference score
- Variants: 147
- Variants ignored: 28
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 140,254
- Population:
- Publication: Schumacher FR et.al, Nat Genet (2018-06-11)
- View in PGS-Catalog
Target study
- Coverage: 104 (70.75%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000032
Reference score
- Variants: 20
- Variants ignored: 5
-
Trait: Type 2 diabetes (based on SNPs involved in β-cell function)
- Mapped Trait(s):
- Samples: 69,033
- Population:
- Publication: Vassy JL et.al, Diabetes (2014-02-11)
- View in PGS-Catalog
Target study
- Coverage: 15 (75%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000033
Reference score
- Variants: 10
- Variants ignored: 1
-
Trait: Type 2 diabetes (based on SNPs involved in insulin resistance)
- Mapped Trait(s):
- Samples: 69,033
- Population:
- Publication: Vassy JL et.al, Diabetes (2014-02-11)
- View in PGS-Catalog
Target study
- Coverage: 9 (90%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000034
Reference score
- Variants: 97
- Variants ignored: 0
-
Trait: Adult Body Mass Index
- Mapped Trait(s):
- Samples: 238,944
- Population:
- European: 99.1%
- Hispanic or Latin American: 0.5%
- African: 0.4%
- Publication: Song M et.al, Diabetes (2017-12-06)
- View in PGS-Catalog
Target study
- Coverage: 0 (0%) zero
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000035
Reference score
- Variants: 1,168
- Variants ignored: 206
-
Trait: Atrial fibrillation
- Mapped Trait(s):
- Samples: 132,118
- Population:
- European: 89.9%
- African: 4.4%
- East Asian: 3.1%
- Hispanic or Latin American: 2.5%
- Publication: Weng LC et.al, Circulation (2017-11-12)
- View in PGS-Catalog
Target study
- Coverage: 901 (77.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000036
Reference score
- Variants: 171,249
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 455,313
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Mahajan A et.al, Nat Genet (2018-10-08)
- View in PGS-Catalog
Target study
- Coverage: 169,912 (99.22%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000037
Reference score
- Variants: 15
- Variants ignored: 0
-
Trait: Asthma
- Mapped Trait(s):
- Samples: 26,475
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Belsky DW et.al, Lancet Respir Med (2013-06-28)
- View in PGS-Catalog
Target study
- Coverage: 0 (0%) zero
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000038
Reference score
- Variants: 90
- Variants ignored: 21
-
Trait: Stroke
- Mapped Trait(s):
- Samples: 446,696
- Population:
- Publication: Rutten-Jacobs LC et.al, BMJ (2018-10-24)
- View in PGS-Catalog
Target study
- Coverage: 67 (74.44%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000039
Reference score
- Variants: 3,225,583
- Variants ignored: 0
-
Trait: Ischaemic stroke
- Mapped Trait(s):
- Samples: 3,202,307
- Population:
- European: 96.8%
- East Asian: 1.3%
- South Asian: 1%
- African: 0.6%
- Hispanic or Latin American: 0.2%
- Greater Middle Eastern: 0.07%
- Additional Asian Ancestries: 0.01%
- Publication: Abraham G et.al, Nat Commun (2019-12-20)
- View in PGS-Catalog
Target study
- Coverage: 3,214,345 (99.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000043
Reference score
- Variants: 297
- Variants ignored: 0
-
Trait: Venous thromboembolism
- Mapped Trait(s):
- Samples: 650,119
- Population:
- European: 88.7%
- African: 7.9%
- Hispanic or Latin American: 3.4%
- Publication: Klarin D et.al, Nat Genet (2019-11-01)
- View in PGS-Catalog
Target study
- Coverage: 297 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000044
Reference score
- Variants: 66
- Variants ignored: 0
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 153,371
- Population:
- European: 95.2%
- East Asian: 4.8%
- Publication: Pashayan N et.al, Br J Cancer (2015-08-20)
- View in PGS-Catalog
Target study
- Coverage: 33 (50%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000045
Reference score
- Variants: 88
- Variants ignored: 0
-
Trait: Breast cancer
- Mapped Trait(s):
- Samples: 22,627
- Population:
- Publication: Kuchenbaecker KB et.al, J Natl Cancer Inst (2017-07-01)
- View in PGS-Catalog
Target study
- Coverage: 59 (67.05%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000046
Reference score
- Variants: 87
- Variants ignored: 0
-
Trait: Estrogen receptor [ER]-positive breast cancer
- Mapped Trait(s):
- Samples: 22,627
- Population:
- Publication: Kuchenbaecker KB et.al, J Natl Cancer Inst (2017-07-01)
- View in PGS-Catalog
Target study
- Coverage: 58 (66.67%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000047
Reference score
- Variants: 53
- Variants ignored: 0
-
Trait: Estrogen receptor [ER]-negative breast cancer
- Mapped Trait(s):
- Samples: 22,627
- Population:
- Publication: Kuchenbaecker KB et.al, J Natl Cancer Inst (2017-07-01)
- View in PGS-Catalog
Target study
- Coverage: 32 (60.38%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000048
Reference score
- Variants: 17
- Variants ignored: 0
-
Trait: Ovarian cancer
- Mapped Trait(s):
- Samples: 13,491
- Population:
- Publication: Kuchenbaecker KB et.al, J Natl Cancer Inst (2017-07-01)
- View in PGS-Catalog
Target study
- Coverage: 16 (94.12%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000049
Reference score
- Variants: 103
- Variants ignored: 22
-
Trait: Prostate Cancer
- Mapped Trait(s):
- Samples: 87,040
- Population:
- European: 77.6%
- African: 12%
- East Asian: 8%
- Hispanic or Latin American: 2.4%
- Publication: Lecarpentier J et.al, J Clin Oncol (2017-04-27)
- View in PGS-Catalog
Target study
- Coverage: 73 (70.87%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000050
Reference score
- Variants: 44
- Variants ignored: 0
-
Trait: Breast cancer
- Mapped Trait(s):
- Samples: 61,693
- Population:
- Publication: Wen W et.al, Breast Cancer Res (2016-12-08)
- View in PGS-Catalog
Target study
- Coverage: 44 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000051
Reference score
- Variants: 67
- Variants ignored: 12
-
Trait: Breast Cancer
- Mapped Trait(s):
- Samples: 22,627
- Population:
- Publication: Zhang X et.al, PLoS Med (2018-09-04)
- View in PGS-Catalog
Target study
- Coverage: 52 (77.61%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000052
Reference score
- Variants: 161
- Variants ignored: 0
-
Trait: Breast cancer
- Mapped Trait(s):
- Samples: 139,274
- Population:
- Publication: Lakeman IMM et.al, J Med Genet (2019-06-11)
- View in PGS-Catalog
Target study
- Coverage: 158 (98.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000053
Reference score
- Variants: 21
- Variants ignored: 7
-
Trait: Alzheimer's disease (late onset)
- Mapped Trait(s):
- Samples: 55,134
- Population:
- Publication: Tosto G et.al, Neurology (2017-02-17)
- View in PGS-Catalog
Target study
- Coverage: 14 (66.67%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000054
Reference score
- Variants: 21
- Variants ignored: 4
-
Trait: Alzheimer's disease (late onset)
- Mapped Trait(s):
- Samples: 55,134
- Population:
- Publication: Tosto G et.al, Neurology (2017-02-17)
- View in PGS-Catalog
Target study
- Coverage: 17 (80.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000055
Reference score
- Variants: 76
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 74,409
- Population:
- European: 91.1%
- African: 8.9%
- Publication: Schmit SL et.al, J Natl Cancer Inst (2019-02-01)
- View in PGS-Catalog
Target study
- Coverage: 76 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000056
Reference score
- Variants: 23
- Variants ignored: 0
-
Trait: Parkinson Disease
- Mapped Trait(s):
- Samples: 108,990
- Population:
- Publication: Paul KC et.al, JAMA Neurol (2018-03-01)
- View in PGS-Catalog
Target study
- Coverage: 21 (91.3%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000057
Reference score
- Variants: 57
- Variants ignored: 9
-
Trait: Coronary heart disease
- Mapped Trait(s):
- Samples: 502,601
- Population:
- European: 52.1%
- Multi-Ancestry (including Europeans): 38.7%
- South Asian: 5.1%
- East Asian: 2.3%
- Hispanic or Latin American: 0.8%
- African: 0.6%
- Greater Middle Eastern: 0.5%
- Publication: Natarajan P et.al, Circulation (2017-02-21)
- View in PGS-Catalog
Target study
- Coverage: 34 (59.65%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000058
Reference score
- Variants: 204
- Variants ignored: 0
-
Trait: Coronary artery disease
- Mapped Trait(s):
- Samples: 1,472,359
- Population:
- European: 41.1%
- Multi-Ancestry (including Europeans): 34.6%
- Unknown: 20.1%
- South Asian: 2.7%
- East Asian: 0.8%
- Hispanic or Latin American: 0.3%
- African: 0.2%
- Greater Middle Eastern: 0.2%
- Publication: Morieri ML et.al, Diabetes Care (2018-09-27)
- View in PGS-Catalog
Target study
- Coverage: 201 (98.53%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000059
Reference score
- Variants: 46
- Variants ignored: 10
-
Trait: Coronary heart disease
- Mapped Trait(s):
- Samples: 540,176
- Population:
- European: 51.4%
- Multi-Ancestry (including Europeans): 36%
- South Asian: 7.5%
- East Asian: 3.4%
- Hispanic or Latin American: 0.8%
- African: 0.6%
- Greater Middle Eastern: 0.4%
- Publication: Hajek C et.al, Circ Genom Precis Med (2018-10-01)
- View in PGS-Catalog
Target study
- Coverage: 35 (76.09%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000060
Reference score
- Variants: 46
- Variants ignored: 0
-
Trait: high-density lipoprotein (HDL) cholesterol
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 99,900
- Population:
- Publication: Johnson L et.al, PLoS One (2015-05-07)
- View in PGS-Catalog
Target study
- Coverage: 46 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000061
Reference score
- Variants: 37
- Variants ignored: 0
-
Trait: low-density lipoprotein (LDL) cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 95,454
- Population:
- Publication: Johnson L et.al, PLoS One (2015-05-07)
- View in PGS-Catalog
Target study
- Coverage: 36 (97.3%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000062
Reference score
- Variants: 52
- Variants ignored: 0
-
Trait: total cholesterol
- Mapped Trait(s):
- Samples: 100,184
- Population:
- Publication: Johnson L et.al, PLoS One (2015-05-07)
- View in PGS-Catalog
Target study
- Coverage: 51 (98.08%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000063
Reference score
- Variants: 32
- Variants ignored: 0
-
Trait: triglycerides
- Mapped Trait(s):
- Samples: 96,598
- Population:
- Publication: Johnson L et.al, PLoS One (2015-05-07)
- View in PGS-Catalog
Target study
- Coverage: 32 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000064
Reference score
- Variants: 120
- Variants ignored: 0
-
Trait: High density lipoprotein (HDL) cholesterol
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 331,368
- Population:
- European: 81.6%
- South Asian: 9.2%
- African: 5.1%
- East Asian: 2.5%
- Hispanic or Latin American: 1.5%
- Publication: Kuchenbaecker K et.al, Nat Commun (2019-09-24)
- View in PGS-Catalog
Target study
- Coverage: 120 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000065
Reference score
- Variants: 103
- Variants ignored: 0
-
Trait: Low density lipoprotein (LDL) cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 331,368
- Population:
- European: 81.6%
- South Asian: 9.2%
- African: 5.1%
- East Asian: 2.5%
- Hispanic or Latin American: 1.5%
- Publication: Kuchenbaecker K et.al, Nat Commun (2019-09-24)
- View in PGS-Catalog
Target study
- Coverage: 103 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000066
Reference score
- Variants: 101
- Variants ignored: 0
-
Trait: Triglycerides (TG)
- Mapped Trait(s):
- Samples: 331,368
- Population:
- European: 81.6%
- South Asian: 9.2%
- African: 5.1%
- East Asian: 2.5%
- Hispanic or Latin American: 1.5%
- Publication: Kuchenbaecker K et.al, Nat Commun (2019-09-24)
- View in PGS-Catalog
Target study
- Coverage: 101 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000067
Reference score
- Variants: 54
- Variants ignored: 0
-
Trait: Prostate cancer
- Mapped Trait(s):
- Publication: Seibert TM et.al, BMJ (2018-01-10)
- View in PGS-Catalog
Target study
- Coverage: 47 (87.04%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000068
Reference score
- Variants: 15
- Variants ignored: 0
-
Trait: Epithelial ovarian cancer
- Mapped Trait(s):
- Samples: 63,347
- Population:
- Publication: Yang X et.al, J Med Genet (2018-05-05)
- View in PGS-Catalog
Target study
- Coverage: 13 (86.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000069
Reference score
- Variants: 15
- Variants ignored: 0
-
Trait: Serous epithelial ovarian cancer
- Mapped Trait(s):
- Samples: 54,990
- Population:
- Publication: Yang X et.al, J Med Genet (2018-05-05)
- View in PGS-Catalog
Target study
- Coverage: 13 (86.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000070
Reference score
- Variants: 19
- Variants ignored: 0
-
Trait: Lung cancer
- Mapped Trait(s):
- Samples: 54,475
- Population:
- European: 51.1%
- East Asian: 48.9%
- Publication: Dai J et.al, Lancet Respir Med (2019-07-17)
- View in PGS-Catalog
Target study
- Coverage: 19 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000071
Reference score
- Variants: 15
- Variants ignored: 0
-
Trait: Bladder cancer
- Mapped Trait(s):
- Samples: 464,396
- Population:
- Publication: Graff RE et.al, Nat Commun (2021-02-12)
- View in PGS-Catalog
Target study
- Coverage: 14 (93.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000072
Reference score
- Variants: 187
- Variants ignored: 59
-
Trait: Breast cancer
- Mapped Trait(s):
- Samples: 419,572
- Population:
- European: 98.1%
- East Asian: 1%
- African: 0.9%
- Publication: Graff RE et.al, Nat Commun (2021-02-12)
- View in PGS-Catalog
Target study
- Coverage: 176 (94.12%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000073
Reference score
- Variants: 10
- Variants ignored: 9
-
Trait: Cervical cancer
- Mapped Trait(s):
- Samples: 20,405
- Population:
- Publication: Graff RE et.al, Nat Commun (2021-02-12)
- View in PGS-Catalog
Target study
- Coverage: 9 (90%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000074
Reference score
- Variants: 103
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 377,666
- Population:
- European: 96.6%
- African: 1.7%
- East Asian: 1.4%
- Additional Diverse Ancestries: 0.3%
- Publication: Graff RE et.al, Nat Commun (2021-02-12)
- View in PGS-Catalog
Target study
- Coverage: 101 (98.06%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000075
Reference score
- Variants: 9
- Variants ignored: 0
-
Trait: Endometrial cancer
- Mapped Trait(s):
- Samples: 43,054
- Population:
- European: 66.4%
- Unknown: 33.6%
- Publication: Graff RE et.al, Nat Commun (2021-02-12)
- View in PGS-Catalog
Target study
- Coverage: 9 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000076
Reference score
- Variants: 19
- Variants ignored: 0
-
Trait: Kidney cancer
- Mapped Trait(s):
- Samples: 42,061
- Population:
- Publication: Graff RE et.al, Nat Commun (2021-02-12)
- View in PGS-Catalog
Target study
- Coverage: 16 (84.21%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000077
Reference score
- Variants: 75
- Variants ignored: 0
-
Trait: Lymphocytic leukemia
- Mapped Trait(s):
- Samples: 145,871
- Population:
- European: 84.3%
- Hispanic or Latin American: 9%
- African: 3.7%
- Multi-Ancestry (excluding Europeans): 3%
- Publication: Graff RE et.al, Nat Commun (2021-02-12)
- View in PGS-Catalog
Target study
- Coverage: 69 (92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000078
Reference score
- Variants: 109
- Variants ignored: 0
-
Trait: Lung cancer
- Mapped Trait(s):
- Samples: 183,537
- Population:
- Publication: Graff RE et.al, Nat Commun (2021-02-12)
- View in PGS-Catalog
Target study
- Coverage: 108 (99.08%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000079
Reference score
- Variants: 24
- Variants ignored: 0
-
Trait: Melanoma
- Mapped Trait(s):
- Samples: 365,516
- Population:
- Publication: Graff RE et.al, Nat Commun (2021-02-12)
- View in PGS-Catalog
Target study
- Coverage: 22 (91.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000080
Reference score
- Variants: 19
- Variants ignored: 9
-
Trait: Non-Hodgkin's lymphoma
- Mapped Trait(s):
- Samples: 34,043
- Population:
- European: 85.3%
- Unknown: 14.7%
- Publication: Graff RE et.al, Nat Commun (2021-02-12)
- View in PGS-Catalog
Target study
- Coverage: 18 (94.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000081
Reference score
- Variants: 14
- Variants ignored: 9
-
Trait: Oral cavity and pharyngeal cancers
- Mapped Trait(s):
- Samples: 20,000
- Population:
- European: 95.6%
- Unknown: 4.4%
- Publication: Graff RE et.al, Nat Commun (2021-02-12)
- View in PGS-Catalog
Target study
- Coverage: 10 (71.43%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000082
Reference score
- Variants: 36
- Variants ignored: 0
-
Trait: Ovarian cancer
- Mapped Trait(s):
- Samples: 152,183
- Population:
- Publication: Graff RE et.al, Nat Commun (2021-02-12)
- View in PGS-Catalog
Target study
- Coverage: 35 (97.22%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000083
Reference score
- Variants: 22
- Variants ignored: 0
-
Trait: Pancreatic cancer
- Mapped Trait(s):
- Samples: 57,275
- Population:
- European: 86.6%
- Unknown: 12.3%
- Multi-Ancestry (excluding Europeans): 1.1%
- Publication: Graff RE et.al, Nat Commun (2021-02-12)
- View in PGS-Catalog
Target study
- Coverage: 22 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000084
Reference score
- Variants: 161
- Variants ignored: 46
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 461,661
- Population:
- European: 93.4%
- African: 2.8%
- East Asian: 2.5%
- Hispanic or Latin American: 1.2%
- Unknown: 0.1%
- Publication: Graff RE et.al, Nat Commun (2021-02-12)
- View in PGS-Catalog
Target study
- Coverage: 152 (94.41%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000086
Reference score
- Variants: 52
- Variants ignored: 0
-
Trait: Testicular cancer
- Mapped Trait(s):
- Samples: 56,799
- Population:
- Publication: Graff RE et.al, Nat Commun (2021-02-12)
- View in PGS-Catalog
Target study
- Coverage: 50 (96.15%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000087
Reference score
- Variants: 12
- Variants ignored: 8
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Samples: 291,738
- Population:
- Publication: Graff RE et.al, Nat Commun (2021-02-12)
- View in PGS-Catalog
Target study
- Coverage: 11 (91.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000088
Reference score
- Variants: 9,121
- Variants ignored: 0
-
Trait: Basophil count
- Mapped Trait(s):
- Samples: 404,718
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 9,014 (98.83%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000089
Reference score
- Variants: 5,248
- Variants ignored: 0
-
Trait: Basophil percentage of white cells
- Mapped Trait(s):
- Samples: 404,532
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 5,196 (99.01%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000090
Reference score
- Variants: 22,949
- Variants ignored: 0
-
Trait: Eosinophil count
- Mapped Trait(s):
- Samples: 406,470
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 22,701 (98.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000091
Reference score
- Variants: 24,406
- Variants ignored: 0
-
Trait: Eosinophil percentage of white cells
- Mapped Trait(s):
- Samples: 406,417
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 24,173 (99.05%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000092
Reference score
- Variants: 28,214
- Variants ignored: 0
-
Trait: Hematocrit
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 27,914 (98.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000093
Reference score
- Variants: 25,090
- Variants ignored: 0
-
Trait: Hemoglobin concentration
- Mapped Trait(s):
- Samples: 407,739
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 24,782 (98.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000094
Reference score
- Variants: 25,493
- Variants ignored: 0
-
Trait: High light scatter reticulocyte count
- Mapped Trait(s):
- Samples: 400,334
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 25,173 (98.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000095
Reference score
- Variants: 21,957
- Variants ignored: 0
-
Trait: High light scatter reticulocyte percentage of red cells
- Mapped Trait(s):
- Samples: 400,438
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 21,694 (98.8%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000096
Reference score
- Variants: 17,850
- Variants ignored: 0
-
Trait: Immature fraction of reticulocytes
- Mapped Trait(s):
- Samples: 396,408
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 17,637 (98.81%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000097
Reference score
- Variants: 24,646
- Variants ignored: 0
-
Trait: Lymphocyte count
- Mapped Trait(s):
- Samples: 407,277
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 24,374 (98.9%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000098
Reference score
- Variants: 22,363
- Variants ignored: 0
-
Trait: Lymphocyte percentage of white cells
- Mapped Trait(s):
- Samples: 407,319
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 22,099 (98.82%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000099
Reference score
- Variants: 27,081
- Variants ignored: 0
-
Trait: Mean corpuscular hemoglobin
- Mapped Trait(s):
- Samples: 406,517
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 26,797 (98.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000100
Reference score
- Variants: 11,832
- Variants ignored: 0
-
Trait: Mean corpuscular hemoglobin concentration
- Mapped Trait(s):
- Samples: 407,850
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 11,686 (98.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000101
Reference score
- Variants: 25,001
- Variants ignored: 0
-
Trait: Mean corpuscular volume
- Mapped Trait(s):
- Samples: 407,157
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 24,717 (98.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000102
Reference score
- Variants: 28,162
- Variants ignored: 0
-
Trait: Monocyte count
- Mapped Trait(s):
- Samples: 403,994
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 27,830 (98.82%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000103
Reference score
- Variants: 22,843
- Variants ignored: 0
-
Trait: Monocyte percentage of white cells
- Mapped Trait(s):
- Samples: 403,136
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 22,603 (98.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000104
Reference score
- Variants: 25,745
- Variants ignored: 0
-
Trait: Mean platelet volume
- Mapped Trait(s):
- Samples: 391,598
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 25,441 (98.82%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000105
Reference score
- Variants: 23,864
- Variants ignored: 0
-
Trait: Neutrophil count
- Mapped Trait(s):
- Samples: 406,788
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 23,604 (98.91%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000106
Reference score
- Variants: 22,049
- Variants ignored: 0
-
Trait: Neutrophil percentage of white cells
- Mapped Trait(s):
- Samples: 407,114
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 21,812 (98.93%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000107
Reference score
- Variants: 30,459
- Variants ignored: 0
-
Trait: Plateletcrit
- Mapped Trait(s):
- Samples: 390,803
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 30,107 (98.84%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000108
Reference score
- Variants: 25,995
- Variants ignored: 0
-
Trait: Platelet distribution width
- Mapped Trait(s):
- Samples: 391,450
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 25,713 (98.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000109
Reference score
- Variants: 26,683
- Variants ignored: 0
-
Trait: Platelet count
- Mapped Trait(s):
- Samples: 391,232
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 26,380 (98.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000110
Reference score
- Variants: 23,242
- Variants ignored: 0
-
Trait: Red blood cell count
- Mapped Trait(s):
- Samples: 408,069
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 22,951 (98.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000111
Reference score
- Variants: 26,077
- Variants ignored: 0
-
Trait: Reticulocyte count
- Mapped Trait(s):
- Samples: 396,720
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 25,795 (98.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000112
Reference score
- Variants: 25,939
- Variants ignored: 0
-
Trait: Reticulocyte fraction of red cells
- Mapped Trait(s):
- Samples: 396,811
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 25,644 (98.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000113
Reference score
- Variants: 28,383
- Variants ignored: 0
-
Trait: White blood cell count
- Mapped Trait(s):
- Samples: 408,032
- Population:
- Publication: Xu Y et.al, Cell Genom (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 28,067 (98.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000114
Reference score
- Variants: 26
- Variants ignored: 2
-
Trait: Juvenile Idiopathic Arthritis
- Mapped Trait(s):
- Publication: Cánovas R et.al, Ann Rheum Dis (2020-09-04)
- View in PGS-Catalog
Target study
- Coverage: 24 (92.31%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000115
Reference score
- Variants: 223
- Variants ignored: 0
-
Trait: low density lipoprotein cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 297,626
- Population:
- European: 72.4%
- African: 19.3%
- Hispanic or Latin American: 8.3%
- Publication: Trinder M et.al, JAMA Cardiol (2020-02-12)
- View in PGS-Catalog
Target study
- Coverage: 221 (99.1%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000116
Reference score
- Variants: 40,079
- Variants ignored: 0
-
Trait: Coronary Artery Disease
- Mapped Trait(s):
- Samples: 187,599
- Population:
- European: 75.3%
- South Asian: 13.6%
- East Asian: 6%
- Hispanic or Latin American: 2.2%
- African: 1.7%
- Greater Middle Eastern: 1.2%
- Publication: Elliott J et.al, JAMA (2020-02-01)
- View in PGS-Catalog
Target study
- Coverage: 40,035 (99.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000117
Reference score
- Variants: 297,862
- Variants ignored: 0
-
Trait: Cardiovascular Disease
- Mapped Trait(s):
- Samples: 187,599
- Population:
- European: 75.3%
- South Asian: 13.6%
- East Asian: 6%
- Hispanic or Latin American: 2.2%
- African: 1.7%
- Greater Middle Eastern: 1.2%
- Publication: Elliott J et.al, JAMA (2020-02-01)
- View in PGS-Catalog
Target study
- Coverage: 297,414 (99.85%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000118
Reference score
- Variants: 29
- Variants ignored: 8
-
Trait: Melanoma
- Mapped Trait(s):
- Publication: Fritsche LG et.al, PLoS Genet (2019-06-13)
- View in PGS-Catalog
Target study
- Coverage: 21 (72.41%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000119
Reference score
- Variants: 32
- Variants ignored: 6
-
Trait: Basal cell carcinoma
- Mapped Trait(s):
- Publication: Fritsche LG et.al, PLoS Genet (2019-06-13)
- View in PGS-Catalog
Target study
- Coverage: 25 (78.12%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000120
Reference score
- Variants: 10
- Variants ignored: 2
-
Trait: Squamous cell carcinoma
- Mapped Trait(s):
- Samples: 287,137
- Population:
- Publication: Fritsche LG et.al, PLoS Genet (2019-06-13)
- View in PGS-Catalog
Target study
- Coverage: 8 (80%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000123
Reference score
- Variants: 16
- Variants ignored: 0
-
Trait: Parkinson disease
- Mapped Trait(s):
- Samples: 108,990
- Population:
- Publication: Ibanez L et.al, BMC Neurol (2017-11-15)
- View in PGS-Catalog
Target study
- Coverage: 16 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000124
Reference score
- Variants: 103
- Variants ignored: 0
-
Trait: Intraocular pressure
- Mapped Trait(s):
- Samples: 157,391
- Population:
- Publication: MacGregor S et.al, Nat Genet (2018-07-27)
- View in PGS-Catalog
Target study
- Coverage: 103 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000125
Reference score
- Variants: 80
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 169,298
- Population:
- European: 40.8%
- East Asian: 26.9%
- African: 14.1%
- South Asian: 11.8%
- Hispanic or Latin American: 6.4%
- Publication: Qi Q et.al, Diabetes (2017-03-02)
- View in PGS-Catalog
Target study
- Coverage: 80 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000126
Reference score
- Variants: 114
- Variants ignored: 0
-
Trait: Serum urate
- Mapped Trait(s):
- Samples: 288,649
- Population:
- Publication: Tin A et.al, Nat Genet (2019-10-02)
- View in PGS-Catalog
Target study
- Coverage: 114 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000133
Reference score
- Variants: 604,645
- Variants ignored: 0
-
Trait: Schizophrenia
- Mapped Trait(s):
- Samples: 87,534
- Population:
- European: 94%
- East Asian: 6%
- Publication: Zheutlin AB et.al, Am J Psychiatry (2019-08-16)
- View in PGS-Catalog
Target study
- Coverage: 604,645 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000134
Reference score
- Variants: 830,589
- Variants ignored: 0
-
Trait: Schizophrenia
- Mapped Trait(s):
- Samples: 87,534
- Population:
- European: 94%
- East Asian: 6%
- Publication: Zheutlin AB et.al, Am J Psychiatry (2019-08-16)
- View in PGS-Catalog
Target study
- Coverage: 830,589 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000135
Reference score
- Variants: 972,439
- Variants ignored: 0
-
Trait: Schizophrenia
- Mapped Trait(s):
- Samples: 87,534
- Population:
- European: 94%
- East Asian: 6%
- Publication: Zheutlin AB et.al, Am J Psychiatry (2019-08-16)
- View in PGS-Catalog
Target study
- Coverage: 972,439 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000136
Reference score
- Variants: 833,502
- Variants ignored: 0
-
Trait: Schizophrenia
- Mapped Trait(s):
- Samples: 87,534
- Population:
- European: 94%
- East Asian: 6%
- Publication: Zheutlin AB et.al, Am J Psychiatry (2019-08-16)
- View in PGS-Catalog
Target study
- Coverage: 833,502 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000137
Reference score
- Variants: 2,673
- Variants ignored: 0
-
Trait: Glaucoma
- Mapped Trait(s):
- Samples: 351,696
- Population:
- Publication: Craig JE et.al, Nat Genet (2020-01-20)
- View in PGS-Catalog
Target study
- Coverage: 2,656 (99.36%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000138
Reference score
- Variants: 22,274
- Variants ignored: 0
-
Trait: Lifetime Major Depressive Disorder
- Mapped Trait(s):
- Samples: 67,171
- Population:
- Publication: Cai N et.al, Nat Genet (2020-03-30)
- View in PGS-Catalog
Target study
- Coverage: 22,270 (99.98%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000139
Reference score
- Variants: 21,980
- Variants ignored: 0
-
Trait: Lifetime Major Depressive Disorder (with recurrence)
- Mapped Trait(s):
- Samples: 59,385
- Population:
- Publication: Cai N et.al, Nat Genet (2020-03-30)
- View in PGS-Catalog
Target study
- Coverage: 21,978 (99.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000140
Reference score
- Variants: 24,665
- Variants ignored: 0
-
Trait: Broad Depression (seen a General Practitioner for nerves, anxiety, tension or depression)
- Mapped Trait(s):
- EFO_0009820: seeing a general practitioner for nerves, anxiety, tension or depression, self-reported
- MONDO_0002050: depressive disorder
- Samples: 332,622
- Population:
- Publication: Cai N et.al, Nat Genet (2020-03-30)
- View in PGS-Catalog
Target study
- Coverage: 24,664 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000141
Reference score
- Variants: 22,728
- Variants ignored: 0
-
Trait: Seen a psychiatrist for nerves, anxiety, tension or depression
- Mapped Trait(s):
- EFO_0009821: seeing a psychiatrist for nerves, anxiety, tension or depression, self-reported
- MONDO_0002050: depressive disorder
- Samples: 333,412
- Population:
- Publication: Cai N et.al, Nat Genet (2020-03-30)
- View in PGS-Catalog
Target study
- Coverage: 22,726 (99.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000142
Reference score
- Variants: 21,908
- Variants ignored: 0
-
Trait: Probable Depression (low mood or anhedonia, and seen a GP or psychiatrist for nerves, anxiety, tension or depression)
- Mapped Trait(s):
- EFO_0009820: seeing a general practitioner for nerves, anxiety, tension or depression, self-reported
- EFO_0009821: seeing a psychiatrist for nerves, anxiety, tension or depression, self-reported
- MONDO_0002050: depressive disorder
- Samples: 80,575
- Population:
- Publication: Cai N et.al, Nat Genet (2020-03-30)
- View in PGS-Catalog
Target study
- Coverage: 21,905 (99.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000143
Reference score
- Variants: 21,042
- Variants ignored: 0
-
Trait: Seen a General Practitioner for nerves, anxiety, tension or depression (without report of low mood or anhedonia)
- Mapped Trait(s):
- EFO_0009820: seeing a general practitioner for nerves, anxiety, tension or depression, self-reported
- Samples: 58,125
- Population:
- Publication: Cai N et.al, Nat Genet (2020-03-30)
- View in PGS-Catalog
Target study
- Coverage: 21,042 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000144
Reference score
- Variants: 21,828
- Variants ignored: 0
-
Trait: Self-reported depression or depression symptoms
- Mapped Trait(s):
- Samples: 253,919
- Population:
- Publication: Cai N et.al, Nat Genet (2020-03-30)
- View in PGS-Catalog
Target study
- Coverage: 21,821 (99.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000145
Reference score
- Variants: 21,510
- Variants ignored: 0
-
Trait: Depression (ICD-10 defined)
- Mapped Trait(s):
- Samples: 212,411
- Population:
- Publication: Cai N et.al, Nat Genet (2020-03-30)
- View in PGS-Catalog
Target study
- Coverage: 21,505 (99.98%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000146
Reference score
- Variants: 27
- Variants ignored: 0
-
Trait: Colorectal cancer risk
- Mapped Trait(s):
- Samples: 106,056
- Population:
- European: 90.5%
- East Asian: 7.4%
- Unknown: 2.1%
- Publication: Hsu L et.al, Gastroenterology (2015-02-13)
- View in PGS-Catalog
Target study
- Coverage: 27 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000147
Reference score
- Variants: 21
- Variants ignored: 4
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 0
- Population:
- Publication: Ibáñez-Sanz G et.al, Sci Rep (2017-02-24)
- View in PGS-Catalog
Target study
- Coverage: 16 (76.19%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000148
Reference score
- Variants: 63
- Variants ignored: 1
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 65,764
- Population:
- Publication: Jeon J et.al, Gastroenterology (2018-02-17)
- View in PGS-Catalog
Target study
- Coverage: 61 (96.83%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000149
Reference score
- Variants: 41
- Variants ignored: 7
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Publication: Smith T et.al, Br J Cancer (2018-10-16)
- View in PGS-Catalog
Target study
- Coverage: 32 (78.05%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000150
Reference score
- Variants: 48
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 179,299
- Population:
- European: 91.9%
- East Asian: 6.3%
- Unknown: 1.2%
- Additional Diverse Ancestries: 0.5%
- Publication: Weigl K et.al, Gastroenterology (2018-03-21)
- View in PGS-Catalog
Target study
- Coverage: 45 (93.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000151
Reference score
- Variants: 14
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Publication: Xin J et.al, Gene (2018-06-14)
- View in PGS-Catalog
Target study
- Coverage: 14 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000152
Reference score
- Variants: 10
- Variants ignored: 1
-
Trait: Bladder cancer
- Mapped Trait(s):
- Samples: 143,819
- Population:
- Publication: Shi Z et.al, Cancer Med (2019-04-09)
- View in PGS-Catalog
Target study
- Coverage: 9 (90%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000153
Reference score
- Variants: 66
- Variants ignored: 17
-
Trait: Breast cancer
- Mapped Trait(s):
- Samples: 102,721
- Population:
- Publication: Shi Z et.al, Cancer Med (2019-04-09)
- View in PGS-Catalog
Target study
- Coverage: 49 (74.24%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000154
Reference score
- Variants: 30
- Variants ignored: 5
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 208,379
- Population:
- European: 96.8%
- African: 3.2%
- Publication: Shi Z et.al, Cancer Med (2019-04-09)
- View in PGS-Catalog
Target study
- Coverage: 25 (83.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000155
Reference score
- Variants: 19
- Variants ignored: 4
-
Trait: Glioma
- Mapped Trait(s):
- Samples: 103,614
- Population:
- Publication: Shi Z et.al, Cancer Med (2019-04-09)
- View in PGS-Catalog
Target study
- Coverage: 15 (78.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000156
Reference score
- Variants: 6
- Variants ignored: 0
-
Trait: Lung cancer
- Mapped Trait(s):
- Samples: 258,478
- Population:
- Publication: Shi Z et.al, Cancer Med (2019-04-09)
- View in PGS-Catalog
Target study
- Coverage: 6 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000157
Reference score
- Variants: 17
- Variants ignored: 4
-
Trait: Melanoma
- Mapped Trait(s):
- Samples: 318,595
- Population:
- Publication: Shi Z et.al, Cancer Med (2019-04-09)
- View in PGS-Catalog
Target study
- Coverage: 13 (76.47%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000158
Reference score
- Variants: 10
- Variants ignored: 1
-
Trait: Ovarian cancer
- Mapped Trait(s):
- Samples: 28,505
- Population:
- Publication: Shi Z et.al, Cancer Med (2019-04-09)
- View in PGS-Catalog
Target study
- Coverage: 9 (90%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000159
Reference score
- Variants: 9
- Variants ignored: 3
-
Trait: Pancreatic cancer
- Mapped Trait(s):
- Samples: 29,698
- Population:
- European: 72.5%
- Unknown: 23.7%
- Multi-Ancestry (excluding Europeans): 2.1%
- Additional Diverse Ancestries: 1.2%
- East Asian: 0.4%
- Publication: Shi Z et.al, Cancer Med (2019-04-09)
- View in PGS-Catalog
Target study
- Coverage: 6 (66.67%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000160
Reference score
- Variants: 79
- Variants ignored: 17
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 349,459
- Population:
- European: 91.8%
- African: 3.6%
- East Asian: 2.9%
- Hispanic or Latin American: 1.6%
- Publication: Shi Z et.al, Cancer Med (2019-04-09)
- View in PGS-Catalog
Target study
- Coverage: 62 (78.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000161
Reference score
- Variants: 10
- Variants ignored: 3
-
Trait: Renal cancer
- Mapped Trait(s):
- Samples: 67,529
- Population:
- Publication: Shi Z et.al, Cancer Med (2019-04-09)
- View in PGS-Catalog
Target study
- Coverage: 7 (70%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000162
Reference score
- Variants: 6
- Variants ignored: 2
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Samples: 355,697
- Population:
- Publication: Shi Z et.al, Cancer Med (2019-04-09)
- View in PGS-Catalog
Target study
- Coverage: 4 (66.67%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000163
Reference score
- Variants: 185
- Variants ignored: 0
-
Trait: Basophil count
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 178 (96.22%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000164
Reference score
- Variants: 150
- Variants ignored: 0
-
Trait: Basophil percentage of white cells
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 144 (96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000165
Reference score
- Variants: 607
- Variants ignored: 0
-
Trait: Eosinophil count
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 588 (96.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000166
Reference score
- Variants: 571
- Variants ignored: 0
-
Trait: Eosinophil percentage of white cells
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 553 (96.85%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000167
Reference score
- Variants: 502
- Variants ignored: 0
-
Trait: Hematocrit
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 481 (95.82%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000168
Reference score
- Variants: 515
- Variants ignored: 0
-
Trait: Hemoglobin concentration
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 492 (95.53%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000169
Reference score
- Variants: 570
- Variants ignored: 0
-
Trait: High light scatter reticulocyte count
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 549 (96.32%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000170
Reference score
- Variants: 566
- Variants ignored: 0
-
Trait: High light scatter reticulocyte percentage of red cells
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 546 (96.47%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000171
Reference score
- Variants: 372
- Variants ignored: 0
-
Trait: Immature fraction of reticulocytes
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 360 (96.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000172
Reference score
- Variants: 621
- Variants ignored: 0
-
Trait: Lymphocyte count
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 609 (98.07%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000173
Reference score
- Variants: 472
- Variants ignored: 0
-
Trait: Lymphocyte percentage of white cells
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 453 (95.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000174
Reference score
- Variants: 628
- Variants ignored: 0
-
Trait: Mean corpuscular hemoglobin
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 604 (96.18%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000175
Reference score
- Variants: 224
- Variants ignored: 0
-
Trait: Mean corpuscular hemoglobin concentration
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 217 (96.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000176
Reference score
- Variants: 685
- Variants ignored: 0
-
Trait: Mean corpuscular volume
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 663 (96.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000177
Reference score
- Variants: 638
- Variants ignored: 0
-
Trait: Monocyte count
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 622 (97.49%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000178
Reference score
- Variants: 549
- Variants ignored: 0
-
Trait: Monocyte percentage of white cells
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 534 (97.27%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000179
Reference score
- Variants: 654
- Variants ignored: 0
-
Trait: Mean platelet volume
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 622 (95.11%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000180
Reference score
- Variants: 629
- Variants ignored: 0
-
Trait: Mean reticulocyte volume
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 607 (96.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000181
Reference score
- Variants: 761
- Variants ignored: 0
-
Trait: Mean sphered corpuscular volume
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 736 (96.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000182
Reference score
- Variants: 492
- Variants ignored: 0
-
Trait: Neutrophil count
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 475 (96.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000183
Reference score
- Variants: 437
- Variants ignored: 0
-
Trait: Neutrophil percentage of white cells
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 423 (96.8%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000184
Reference score
- Variants: 700
- Variants ignored: 0
-
Trait: Plateletcrit
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 681 (97.29%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000185
Reference score
- Variants: 555
- Variants ignored: 0
-
Trait: Platelet distribution width
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 539 (97.12%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000186
Reference score
- Variants: 739
- Variants ignored: 0
-
Trait: Platelet count
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 710 (96.08%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000187
Reference score
- Variants: 678
- Variants ignored: 0
-
Trait: Red blood cell count
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 656 (96.76%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000188
Reference score
- Variants: 546
- Variants ignored: 0
-
Trait: Red cell distribution width
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 530 (97.07%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000189
Reference score
- Variants: 555
- Variants ignored: 0
-
Trait: Reticulocyte count
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 537 (96.76%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000190
Reference score
- Variants: 537
- Variants ignored: 0
-
Trait: Reticulocyte fraction of red cells
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 519 (96.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000191
Reference score
- Variants: 636
- Variants ignored: 0
-
Trait: White blood cell count
- Mapped Trait(s):
- Samples: 408,112
- Population:
- Publication: Vuckovic D et.al, Cell (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 617 (97.01%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000193
Reference score
- Variants: 1,138
- Variants ignored: 0
-
Trait: Major depression
- Mapped Trait(s):
- Samples: 431,394
- Population:
- Publication: Coleman JRI et.al, Mol Psychiatry (2020-01-23)
- View in PGS-Catalog
Target study
- Coverage: 1,132 (99.47%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000194
Reference score
- Variants: 250
- Variants ignored: 0
-
Trait: Rheumatoid Arthritis (CCP-positive)
- Mapped Trait(s):
- Samples: 191,461
- Population:
- European: 88.2%
- East Asian: 11.8%
- Publication: Knevel R et.al, Sci Transl Med (2020-05-01)
- View in PGS-Catalog
Target study
- Coverage: 198 (79.2%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000195
Reference score
- Variants: 250
- Variants ignored: 0
-
Trait: Rheumatoid Arthritis (CCP-negative)
- Mapped Trait(s):
- Samples: 191,461
- Population:
- European: 88.2%
- East Asian: 11.8%
- Publication: Knevel R et.al, Sci Transl Med (2020-05-01)
- View in PGS-Catalog
Target study
- Coverage: 198 (79.2%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000196
Reference score
- Variants: 250
- Variants ignored: 0
-
Trait: Systemic lupus eythematosus
- Mapped Trait(s):
- Samples: 26,599
- Population:
- Publication: Knevel R et.al, Sci Transl Med (2020-05-01)
- View in PGS-Catalog
Target study
- Coverage: 198 (79.2%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000197
Reference score
- Variants: 250
- Variants ignored: 0
-
Trait: Spondyloarthroparthy
- Mapped Trait(s):
- Samples: 32,957
- Population:
- European: 90.5%
- East Asian: 9.5%
- Publication: Knevel R et.al, Sci Transl Med (2020-05-01)
- View in PGS-Catalog
Target study
- Coverage: 198 (79.2%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000198
Reference score
- Variants: 250
- Variants ignored: 0
-
Trait: Psoriatic arthritis
- Mapped Trait(s):
- Samples: 103,432
- Population:
- European: 78.2%
- East Asian: 21.8%
- Publication: Knevel R et.al, Sci Transl Med (2020-05-01)
- View in PGS-Catalog
Target study
- Coverage: 198 (79.2%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000199
Reference score
- Variants: 250
- Variants ignored: 0
-
Trait: Gout
- Mapped Trait(s):
- Samples: 110,347
- Population:
- Publication: Knevel R et.al, Sci Transl Med (2020-05-01)
- View in PGS-Catalog
Target study
- Coverage: 198 (79.2%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000200
Reference score
- Variants: 28
- Variants ignored: 4
-
Trait: Coronary heart disease
- Mapped Trait(s):
- Samples: 126,029
- Population:
- European: 88.3%
- South Asian: 11.7%
- Publication: Tikkanen E et.al, Arterioscler Thromb Vasc Biol (2013-04-18)
- View in PGS-Catalog
Target study
- Coverage: 24 (85.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000201
Reference score
- Variants: 1,094,954
- Variants ignored: 0
-
Trait: Problematic Alcohol Use
- Mapped Trait(s):
- Samples: 166,604
- Population:
- Publication: Barr PB et.al, Transl Psychiatry (2020-06-18)
- View in PGS-Catalog
Target study
- Coverage: 1,094,954 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000202
Reference score
- Variants: 1,083,002
- Variants ignored: 0
-
Trait: Problematic Alcohol Use
- Mapped Trait(s):
- Samples: 166,604
- Population:
- Publication: Barr PB et.al, Transl Psychiatry (2020-06-18)
- View in PGS-Catalog
Target study
- Coverage: 1,083,002 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000203
Reference score
- Variants: 1,110,910
- Variants ignored: 0
-
Trait: Alcohol consumption (drinks per week)
- Mapped Trait(s):
- Samples: 534,683
- Population:
- Publication: Barr PB et.al, Transl Psychiatry (2020-06-18)
- View in PGS-Catalog
Target study
- Coverage: 1,110,910 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000204
Reference score
- Variants: 1,099,480
- Variants ignored: 0
-
Trait: Alcohol consumption (drinks per week)
- Mapped Trait(s):
- Samples: 534,683
- Population:
- Publication: Barr PB et.al, Transl Psychiatry (2020-06-18)
- View in PGS-Catalog
Target study
- Coverage: 1,099,480 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000205
Reference score
- Variants: 1,110,737
- Variants ignored: 0
-
Trait: Risk-taking tendency (4-domain principal component model)
- Mapped Trait(s):
- Samples: 315,894
- Population:
- Publication: Barr PB et.al, Transl Psychiatry (2020-06-18)
- View in PGS-Catalog
Target study
- Coverage: 1,110,737 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000206
Reference score
- Variants: 1,098,765
- Variants ignored: 0
-
Trait: Risk-taking tendency (4-domain principal component model)
- Mapped Trait(s):
- Samples: 315,894
- Population:
- Publication: Barr PB et.al, Transl Psychiatry (2020-06-18)
- View in PGS-Catalog
Target study
- Coverage: 1,098,765 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000207
Reference score
- Variants: 10
- Variants ignored: 0
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Samples: 695,822
- Population:
- Publication: Liyanarachchi S et.al, Proc Natl Acad Sci U S A (2020-03-04)
- View in PGS-Catalog
Target study
- Coverage: 10 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000208
Reference score
- Variants: 10
- Variants ignored: 0
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Samples: 419,036
- Population:
- Publication: Liyanarachchi S et.al, Proc Natl Acad Sci U S A (2020-03-04)
- View in PGS-Catalog
Target study
- Coverage: 10 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000209
Reference score
- Variants: 10
- Variants ignored: 0
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Samples: 290,551
- Population:
- Publication: Liyanarachchi S et.al, Proc Natl Acad Sci U S A (2020-03-04)
- View in PGS-Catalog
Target study
- Coverage: 10 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000210
Reference score
- Variants: 279
- Variants ignored: 0
-
Trait: Lung function (FEV1/FVC)
- Mapped Trait(s):
- Samples: 321,047
- Population:
- Publication: Shrine N et.al, Nat Genet (2019-02-25)
- View in PGS-Catalog
Target study
- Coverage: 277 (99.28%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000211
Reference score
- Variants: 19
- Variants ignored: 2
-
Trait: Parkinson's disease
- Mapped Trait(s):
- Samples: 108,990
- Population:
- Publication: Pihlstrøm L et.al, Mov Disord (2016-02-08)
- View in PGS-Catalog
Target study
- Coverage: 15 (78.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000212
Reference score
- Variants: 330
- Variants ignored: 0
-
Trait: Breast cancer intrinsic-like subtype (luminal A-like)
- Mapped Trait(s):
- Samples: 197,755
- Population:
- Publication: Zhang H et.al, Nat Genet (2020-05-18)
- View in PGS-Catalog
Target study
- Coverage: 330 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000213
Reference score
- Variants: 330
- Variants ignored: 0
-
Trait: Breast cancer intrinsic-like subtype (luminal B/HER2-negative-like)
- Mapped Trait(s):
- Samples: 197,755
- Population:
- Publication: Zhang H et.al, Nat Genet (2020-05-18)
- View in PGS-Catalog
Target study
- Coverage: 330 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000214
Reference score
- Variants: 330
- Variants ignored: 0
-
Trait: Breast cancer intrinsic-like subtype (luminal B-like)
- Mapped Trait(s):
- Samples: 197,755
- Population:
- Publication: Zhang H et.al, Nat Genet (2020-05-18)
- View in PGS-Catalog
Target study
- Coverage: 330 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000215
Reference score
- Variants: 330
- Variants ignored: 0
-
Trait: Breast cancer intrinsic-like subtype (HER2-enriched-like)
- Mapped Trait(s):
- Samples: 197,755
- Population:
- Publication: Zhang H et.al, Nat Genet (2020-05-18)
- View in PGS-Catalog
Target study
- Coverage: 330 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000216
Reference score
- Variants: 330
- Variants ignored: 0
-
Trait: Breast cancer intrinsic-like subtype (triple negative)
- Mapped Trait(s):
- Samples: 197,755
- Population:
- Publication: Zhang H et.al, Nat Genet (2020-05-18)
- View in PGS-Catalog
Target study
- Coverage: 330 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000217
Reference score
- Variants: 552,254
- Variants ignored: 134,528
-
Trait: Adrenomedullin (ADM) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,402 (75.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000218
Reference score
- Variants: 552,121
- Variants ignored: 134,468
-
Trait: Agouti-related protein (AGRP) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,325 (75.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000219
Reference score
- Variants: 553,819
- Variants ignored: 134,531
-
Trait: Ovarian cancer-related tumor marker CA 125 (CA-125) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 418,946 (75.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000220
Reference score
- Variants: 551,989
- Variants ignored: 134,406
-
Trait: C-C motif chemokine 20 (CCL20) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,259 (75.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000221
Reference score
- Variants: 552,347
- Variants ignored: 134,496
-
Trait: C-C motif chemokine 3 (CCL3) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,535 (75.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000222
Reference score
- Variants: 552,214
- Variants ignored: 134,718
-
Trait: C-C motif chemokine 4 (CCL4) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,169 (75.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000223
Reference score
- Variants: 552,187
- Variants ignored: 134,453
-
Trait: Tumor necrosis factor receptor superfamily member 5 (CD40) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,417 (75.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000224
Reference score
- Variants: 552,106
- Variants ignored: 134,145
-
Trait: Chitinase-3-like protein 1 (CHI3L1) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,643 (75.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000225
Reference score
- Variants: 552,163
- Variants ignored: 134,598
-
Trait: Macrophage colony-stimulating factor 1 (CSF-1) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,239 (75.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000226
Reference score
- Variants: 552,195
- Variants ignored: 134,695
-
Trait: Cystatin-B (CSTB) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,186 (75.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000227
Reference score
- Variants: 552,134
- Variants ignored: 134,533
-
Trait: Cathepsin D (CTSD) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,282 (75.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000228
Reference score
- Variants: 552,084
- Variants ignored: 134,518
-
Trait: Cathepsin L1 (CTSL1) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,252 (75.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000229
Reference score
- Variants: 552,274
- Variants ignored: 134,530
-
Trait: Fractalkine (CX3CL1) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,420 (75.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000230
Reference score
- Variants: 552,234
- Variants ignored: 134,342
-
Trait: C-X-C motif chemokine 1 (CXCL1) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,575 (75.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000231
Reference score
- Variants: 552,241
- Variants ignored: 134,672
-
Trait: C-X-C motif chemokine 16 (CXCL16) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,249 (75.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000232
Reference score
- Variants: 552,061
- Variants ignored: 134,850
-
Trait: C-X-C motif chemokine 6 (CXCL6) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 416,891 (75.52%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000233
Reference score
- Variants: 552,067
- Variants ignored: 134,280
-
Trait: Dickkopf-related protein 1 (Dkk-1) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,470 (75.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000234
Reference score
- Variants: 553,046
- Variants ignored: 134,328
-
Trait: Eosinophil cationic protein (ECP) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 418,396 (75.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000235
Reference score
- Variants: 553,163
- Variants ignored: 134,363
-
Trait: Epidermal growth factor (EGF) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 418,472 (75.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000236
Reference score
- Variants: 553,240
- Variants ignored: 134,888
-
Trait: Endothelial cell-specific molecule 1 (ESM-1) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 418,034 (75.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000237
Reference score
- Variants: 552,343
- Variants ignored: 134,322
-
Trait: Fatty acid-binding protein, adipocyte (FABP4) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,695 (75.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000238
Reference score
- Variants: 552,335
- Variants ignored: 134,448
-
Trait: Tumor necrosis factor receptor superfamily member 6 (FAS) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,565 (75.6%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000239
Reference score
- Variants: 552,100
- Variants ignored: 134,354
-
Trait: Fibroblast growth factor 23 (FGF-23) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,429 (75.61%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000240
Reference score
- Variants: 552,138
- Variants ignored: 134,613
-
Trait: Follistatin (FS) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,211 (75.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000241
Reference score
- Variants: 553,548
- Variants ignored: 134,476
-
Trait: Galanin peptides (GAL) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 418,747 (75.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000242
Reference score
- Variants: 552,282
- Variants ignored: 134,319
-
Trait: Galectin-3 (Gal-3) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,636 (75.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000243
Reference score
- Variants: 552,228
- Variants ignored: 134,780
-
Trait: Growth/differentiation factor 15 (GDF-15) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,133 (75.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000244
Reference score
- Variants: 552,236
- Variants ignored: 134,302
-
Trait: Growth hormone (GH) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,624 (75.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000245
Reference score
- Variants: 552,108
- Variants ignored: 134,119
-
Trait: Proheparin-binding EGF-like growth factor (HB-EGF) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,669 (75.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000246
Reference score
- Variants: 552,104
- Variants ignored: 134,554
-
Trait: Hepatocyte growth factor (HGF) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,221 (75.57%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000247
Reference score
- Variants: 553,239
- Variants ignored: 134,742
-
Trait: Kallikrein-11 (hK11) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 418,179 (75.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000248
Reference score
- Variants: 552,212
- Variants ignored: 134,491
-
Trait: Heat shock 27 kDa protein (HSP_27) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,407 (75.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000249
Reference score
- Variants: 552,186
- Variants ignored: 134,455
-
Trait: Interleukin-18 (IL-18) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,405 (75.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000250
Reference score
- Variants: 551,917
- Variants ignored: 134,324
-
Trait: Interleukin-1 receptor antagonist protein (IL-1ra) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,267 (75.6%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000251
Reference score
- Variants: 552,026
- Variants ignored: 134,433
-
Trait: Interleukin-27 (IL-27) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,259 (75.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000252
Reference score
- Variants: 552,426
- Variants ignored: 134,618
-
Trait: Interleukin-6 (IL-6) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,489 (75.57%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000253
Reference score
- Variants: 552,132
- Variants ignored: 134,562
-
Trait: Interleukin-6 receptor subunit alpha (IL-6RA) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,259 (75.57%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000254
Reference score
- Variants: 551,990
- Variants ignored: 134,481
-
Trait: Interleukin-8 (IL-8) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,182 (75.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000255
Reference score
- Variants: 551,884
- Variants ignored: 134,323
-
Trait: Pro-interleukin-16 (IL16) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,245 (75.6%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000256
Reference score
- Variants: 552,423
- Variants ignored: 135,109
-
Trait: Melusin (ITGB1BP2) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 416,985 (75.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000257
Reference score
- Variants: 552,062
- Variants ignored: 134,494
-
Trait: Kidney injury molecule 1 (KIM-1) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,236 (75.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000258
Reference score
- Variants: 552,053
- Variants ignored: 134,541
-
Trait: Kallikrein-6 (KLK6) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,186 (75.57%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000259
Reference score
- Variants: 552,110
- Variants ignored: 134,508
-
Trait: Leptin (LEP) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,284 (75.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000260
Reference score
- Variants: 552,045
- Variants ignored: 134,652
-
Trait: Lectin-like oxidized LDL receptor 1 (LOX-1) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,080 (75.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000261
Reference score
- Variants: 553,070
- Variants ignored: 134,300
-
Trait: Membrane-bound aminopeptidase P (mAmP) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 418,444 (75.66%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000262
Reference score
- Variants: 552,171
- Variants ignored: 134,733
-
Trait: Myoglobin (MB) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,122 (75.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000263
Reference score
- Variants: 552,000
- Variants ignored: 134,918
-
Trait: Monocyte chemotactic protein 1 (MCP-1) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 416,767 (75.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000264
Reference score
- Variants: 552,116
- Variants ignored: 134,613
-
Trait: Matrix metalloproteinase-1 (MMP-1) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,189 (75.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000265
Reference score
- Variants: 552,072
- Variants ignored: 134,559
-
Trait: Matrix metalloproteinase-10 (MMP-10) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,211 (75.57%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000266
Reference score
- Variants: 552,021
- Variants ignored: 134,458
-
Trait: Matrix metalloproteinase-12 (MMP-12) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,240 (75.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000267
Reference score
- Variants: 552,328
- Variants ignored: 134,887
-
Trait: Matrix metalloproteinase-3 (MMP-3) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,118 (75.52%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000268
Reference score
- Variants: 552,052
- Variants ignored: 134,412
-
Trait: Matrix metalloproteinase-7 (MMP-7) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,320 (75.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000269
Reference score
- Variants: 552,278
- Variants ignored: 134,502
-
Trait: Myeloperoxidase (MPO) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,457 (75.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000270
Reference score
- Variants: 554,137
- Variants ignored: 135,006
-
Trait: N-terminal prohormone brain natriuretic peptide (NT-pro_BNP) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 418,808 (75.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000271
Reference score
- Variants: 552,205
- Variants ignored: 134,607
-
Trait: Osteoprotegerin (OPG) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,270 (75.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000272
Reference score
- Variants: 552,298
- Variants ignored: 134,538
-
Trait: Pappalysin-1 (PAPPA) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,434 (75.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000273
Reference score
- Variants: 552,202
- Variants ignored: 134,220
-
Trait: Proteinase-activated receptor 1 (PAR-1) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,666 (75.64%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000274
Reference score
- Variants: 552,265
- Variants ignored: 134,408
-
Trait: Platelet-derived growth factor subunit B (PDGF_subunit_B) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,541 (75.61%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000275
Reference score
- Variants: 552,010
- Variants ignored: 134,364
-
Trait: Platelet endothelial cell adhesion molecule (PECAM-1) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,331 (75.6%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000276
Reference score
- Variants: 552,275
- Variants ignored: 134,539
-
Trait: Placenta growth factor (PlGF) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,407 (75.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000277
Reference score
- Variants: 552,165
- Variants ignored: 134,505
-
Trait: P-selectin glycoprotein ligand 1 (PSGL-1) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,337 (75.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000278
Reference score
- Variants: 552,474
- Variants ignored: 134,775
-
Trait: Pentraxin-related protein PTX3 (PTX3) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,376 (75.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000279
Reference score
- Variants: 552,298
- Variants ignored: 134,624
-
Trait: Receptor for advanced glycosylation end products (RAGE) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,349 (75.57%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000280
Reference score
- Variants: 552,078
- Variants ignored: 134,423
-
Trait: Renin (REN) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,336 (75.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000281
Reference score
- Variants: 552,002
- Variants ignored: 134,834
-
Trait: Resistin (RETN) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 416,850 (75.52%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000282
Reference score
- Variants: 552,420
- Variants ignored: 134,889
-
Trait: Stem cell factor (SCF) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,204 (75.52%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000283
Reference score
- Variants: 552,703
- Variants ignored: 134,824
-
Trait: Spondin-1 (SPON1) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,558 (75.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000284
Reference score
- Variants: 552,006
- Variants ignored: 134,450
-
Trait: ST2 protein (ST2) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,236 (75.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000285
Reference score
- Variants: 552,228
- Variants ignored: 134,455
-
Trait: Tissue factor (TF) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,452 (75.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000286
Reference score
- Variants: 552,241
- Variants ignored: 134,431
-
Trait: Thrombomodulin (TM) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,486 (75.6%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000287
Reference score
- Variants: 552,317
- Variants ignored: 134,780
-
Trait: Tumor necrosis factor receptor 1 (TNF-R1) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,224 (75.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000288
Reference score
- Variants: 552,185
- Variants ignored: 134,685
-
Trait: Tumor necrosis factor receptor 2 (TNF-R2) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,182 (75.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000289
Reference score
- Variants: 552,048
- Variants ignored: 134,383
-
Trait: Tumor necrosis factor ligand superfamily member 14 (TNFSF14) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,341 (75.6%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000290
Reference score
- Variants: 552,279
- Variants ignored: 134,237
-
Trait: TNF-related apoptosis-inducing ligand (TRAIL) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,725 (75.64%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000291
Reference score
- Variants: 552,198
- Variants ignored: 134,289
-
Trait: TNF-related apoptosis-inducing ligand receptor 2 (TRAIL-R2) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,587 (75.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000292
Reference score
- Variants: 552,090
- Variants ignored: 134,430
-
Trait: TNF-related activation-induced cytokine (TRANCE) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,337 (75.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000293
Reference score
- Variants: 552,048
- Variants ignored: 134,338
-
Trait: Urokinase plasminogen activator surface receptor (U-PAR) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,395 (75.61%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000294
Reference score
- Variants: 552,070
- Variants ignored: 134,454
-
Trait: Vascular endothelial growth factor A (VEGF-A) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 417,311 (75.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000295
Reference score
- Variants: 551,905
- Variants ignored: 134,630
-
Trait: Vascular endothelial growth factor D (VEGF-D) serum levels
- Mapped Trait(s):
- Publication: Folkersen L et.al, Nat Metab (2020-10-16)
- View in PGS-Catalog
Target study
- Coverage: 416,952 (75.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000296
Reference score
- Variants: 6,630,150
- Variants ignored: 0
-
Trait: Coronary artery disease
- Mapped Trait(s):
- Samples: 187,599
- Population:
- European: 75.3%
- South Asian: 13.6%
- East Asian: 6%
- Hispanic or Latin American: 2.2%
- African: 1.7%
- Greater Middle Eastern: 1.2%
- Publication: Wang M et.al, J Am Coll Cardiol (2020-08-01)
- View in PGS-Catalog
Target study
- Coverage: 6,630,150 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000297
Reference score
- Variants: 3,290
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 693,529
- Population:
- European: 65.8%
- Unknown: 34.2%
- Publication: Xie T et.al, Circ Genom Precis Med (2020-06-11)
- View in PGS-Catalog
Target study
- Coverage: 3,278 (99.64%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000298
Reference score
- Variants: 941
- Variants ignored: 0
-
Trait: Body mass index
- Mapped Trait(s):
- Samples: 681,275
- Population:
- European: 67%
- Unknown: 33%
- Publication: Xie T et.al, Circ Genom Precis Med (2020-06-11)
- View in PGS-Catalog
Target study
- Coverage: 938 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000299
Reference score
- Variants: 462
- Variants ignored: 0
-
Trait: Waist-to-hip ratio (body mass index adjusted)
- Mapped Trait(s):
- Samples: 379,501
- Population:
- Publication: Xie T et.al, Circ Genom Precis Med (2020-06-11)
- View in PGS-Catalog
Target study
- Coverage: 456 (98.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000300
Reference score
- Variants: 80
- Variants ignored: 0
-
Trait: Heart rate
- Mapped Trait(s):
- Samples: 238,703
- Population:
- European: 97.3%
- Additional Asian Ancestries: 1%
- African: 0.7%
- Unknown: 0.6%
- Additional Diverse Ancestries: 0.3%
- Publication: Xie T et.al, Circ Genom Precis Med (2020-06-11)
- View in PGS-Catalog
Target study
- Coverage: 80 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000301
Reference score
- Variants: 970
- Variants ignored: 0
-
Trait: Systolic blood pressure
- Mapped Trait(s):
- Samples: 757,601
- Population:
- Publication: Xie T et.al, Circ Genom Precis Med (2020-06-11)
- View in PGS-Catalog
Target study
- Coverage: 964 (99.38%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000302
Reference score
- Variants: 962
- Variants ignored: 0
-
Trait: Diastolic blood pressure
- Mapped Trait(s):
- Samples: 757,601
- Population:
- Publication: Xie T et.al, Circ Genom Precis Med (2020-06-11)
- View in PGS-Catalog
Target study
- Coverage: 956 (99.38%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000303
Reference score
- Variants: 253
- Variants ignored: 0
-
Trait: Estimated glomerular filtration rate
- Mapped Trait(s):
- Samples: 567,460
- Population:
- Publication: Xie T et.al, Circ Genom Precis Med (2020-06-11)
- View in PGS-Catalog
Target study
- Coverage: 253 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000304
Reference score
- Variants: 43
- Variants ignored: 0
-
Trait: HbA1c
- Mapped Trait(s):
- Samples: 121,963
- Population:
- European: 72.4%
- East Asian: 15.1%
- South Asian: 6.2%
- African: 6.2%
- Publication: Xie T et.al, Circ Genom Precis Med (2020-06-11)
- View in PGS-Catalog
Target study
- Coverage: 42 (97.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000305
Reference score
- Variants: 31
- Variants ignored: 0
-
Trait: Fasting glucose
- Mapped Trait(s):
- Samples: 146,817
- Population:
- Publication: Xie T et.al, Circ Genom Precis Med (2020-06-11)
- View in PGS-Catalog
Target study
- Coverage: 31 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000306
Reference score
- Variants: 19
- Variants ignored: 0
-
Trait: Fasting glucose (body mass index adjusted)
- Mapped Trait(s):
- EFO_0008036: BMI-adjusted fasting blood glucose measurement
- Samples: 191,084
- Population:
- Publication: Xie T et.al, Circ Genom Precis Med (2020-06-11)
- View in PGS-Catalog
Target study
- Coverage: 19 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000307
Reference score
- Variants: 12
- Variants ignored: 0
-
Trait: Fasting insulin
- Mapped Trait(s):
- Samples: 51,750
- Population:
- Publication: Xie T et.al, Circ Genom Precis Med (2020-06-11)
- View in PGS-Catalog
Target study
- Coverage: 12 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000308
Reference score
- Variants: 12
- Variants ignored: 0
-
Trait: Fasting insulin (body mass index adjusted)
- Mapped Trait(s):
- EFO_0008037: BMI-adjusted fasting blood insulin measurement
- Samples: 51,750
- Population:
- Publication: Xie T et.al, Circ Genom Precis Med (2020-06-11)
- View in PGS-Catalog
Target study
- Coverage: 12 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000309
Reference score
- Variants: 247
- Variants ignored: 0
-
Trait: High-density lipoprotein
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 393,811
- Population:
- Publication: Xie T et.al, Circ Genom Precis Med (2020-06-11)
- View in PGS-Catalog
Target study
- Coverage: 236 (95.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000310
Reference score
- Variants: 194
- Variants ignored: 0
-
Trait: Low-density lipoprotein
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 390,003
- Population:
- Publication: Xie T et.al, Circ Genom Precis Med (2020-06-11)
- View in PGS-Catalog
Target study
- Coverage: 190 (97.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000311
Reference score
- Variants: 234
- Variants ignored: 0
-
Trait: Total cholesterol
- Mapped Trait(s):
- Samples: 393,811
- Population:
- Publication: Xie T et.al, Circ Genom Precis Med (2020-06-11)
- View in PGS-Catalog
Target study
- Coverage: 232 (99.15%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000312
Reference score
- Variants: 190
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 393,811
- Population:
- Publication: Xie T et.al, Circ Genom Precis Med (2020-06-11)
- View in PGS-Catalog
Target study
- Coverage: 186 (97.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000313
Reference score
- Variants: 49
- Variants ignored: 0
-
Trait: Lipoprotein(a)
- Mapped Trait(s):
- Samples: 13,781
- Population:
- Publication: Xie T et.al, Circ Genom Precis Med (2020-06-11)
- View in PGS-Catalog
Target study
- Coverage: 49 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000314
Reference score
- Variants: 77
- Variants ignored: 0
-
Trait: C-reactive protein
- Mapped Trait(s):
- Samples: 204,402
- Population:
- Publication: Xie T et.al, Circ Genom Precis Med (2020-06-11)
- View in PGS-Catalog
Target study
- Coverage: 77 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000315
Reference score
- Variants: 7
- Variants ignored: 0
-
Trait: Immunoglobulin E (IgE)
- Mapped Trait(s):
- Samples: 6,819
- Population:
- Publication: Xie T et.al, Circ Genom Precis Med (2020-06-11)
- View in PGS-Catalog
Target study
- Coverage: 7 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000318
Reference score
- Variants: 4,122
- Variants ignored: 0
-
Trait: All-cause mortality (female)
- Mapped Trait(s):
- Samples: 3,653,882
- Population:
- European: 91.4%
- Unknown: 6.2%
- East Asian: 1.2%
- African: 0.6%
- South Asian: 0.3%
- Additional Asian Ancestries: 0.3%
- Hispanic or Latin American: 0.04%
- Publication: Meisner A et.al, Am J Hum Genet (2020-07-26)
- View in PGS-Catalog
Target study
- Coverage: 3,820 (92.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000319
Reference score
- Variants: 4,092
- Variants ignored: 0
-
Trait: All-cause mortality (male)
- Mapped Trait(s):
- Samples: 3,653,882
- Population:
- European: 91.4%
- Unknown: 6.2%
- East Asian: 1.2%
- African: 0.6%
- South Asian: 0.3%
- Additional Asian Ancestries: 0.3%
- Hispanic or Latin American: 0.04%
- Publication: Meisner A et.al, Am J Hum Genet (2020-07-26)
- View in PGS-Catalog
Target study
- Coverage: 3,792 (92.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000320
Reference score
- Variants: 263,640
- Variants ignored: 55,706
-
Trait: Body mass index
- Mapped Trait(s):
- Samples: 238,944
- Population:
- European: 99.1%
- Hispanic or Latin American: 0.5%
- African: 0.4%
- Publication: Chami N et.al, PLoS Med (2020-07-21)
- View in PGS-Catalog
Target study
- Coverage: 207,368 (78.66%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000321
Reference score
- Variants: 7,319
- Variants ignored: 0
-
Trait: Serum testosterone levels
- Mapped Trait(s):
- Publication: Flynn E et.al, Eur J Hum Genet (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 6,943 (94.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000322
Reference score
- Variants: 7,168
- Variants ignored: 0
-
Trait: Serum testosterone levels in females
- Mapped Trait(s):
- Publication: Flynn E et.al, Eur J Hum Genet (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 6,954 (97.01%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000323
Reference score
- Variants: 8,235
- Variants ignored: 0
-
Trait: Serum testosterone levels in males
- Mapped Trait(s):
- Publication: Flynn E et.al, Eur J Hum Genet (2020-09-01)
- View in PGS-Catalog
Target study
- Coverage: 7,508 (91.17%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000324
Reference score
- Variants: 138
- Variants ignored: 3
-
Trait: Enthesitis-related Juvenile Idiophatic Arthritis
- Mapped Trait(s):
- EFO_0009732: enthesitis-related juvenile idiopathic arthritis
- Publication: Cánovas R et.al, Ann Rheum Dis (2020-09-04)
- View in PGS-Catalog
Target study
- Coverage: 131 (94.93%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000325
Reference score
- Variants: 21
- Variants ignored: 3
-
Trait: Oligoarthritis Juvenile Idiophatic Arthritis
- Mapped Trait(s):
- EFO_1002019: oligoarticular juvenile idiopathic arthritis
- Publication: Cánovas R et.al, Ann Rheum Dis (2020-09-04)
- View in PGS-Catalog
Target study
- Coverage: 18 (85.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000326
Reference score
- Variants: 12
- Variants ignored: 1
-
Trait: Rheumatoid-factor-negative Polyarthritis (Juvenile Idiophatic Arthritis)
- Mapped Trait(s):
- EFO_1002020: polyarticular juvenile idiopathic arthritis, rheumatoid factor negative
- Publication: Cánovas R et.al, Ann Rheum Dis (2020-09-04)
- View in PGS-Catalog
Target study
- Coverage: 11 (91.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000327
Reference score
- Variants: 35,087
- Variants ignored: 0
-
Trait: Autism spectrum disorder
- Mapped Trait(s):
- Samples: 46,350
- Population:
- Publication: Grove J et.al, Nat Genet (2019-02-25)
- View in PGS-Catalog
Target study
- Coverage: 35,086 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000328
Reference score
- Variants: 57
- Variants ignored: 6
-
Trait: Systemic lupus erythematosus
- Mapped Trait(s):
- Samples: 14,267
- Population:
- Publication: Reid S et.al, Ann Rheum Dis (2019-12-11)
- View in PGS-Catalog
Target study
- Coverage: 18 (31.58%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000329
Reference score
- Variants: 6,423,165
- Variants ignored: 0
-
Trait: Coronary heart disease
- Mapped Trait(s):
- Samples: 408,458
- Population:
- Publication: Mars N et.al, Nat Med (2020-04-07)
- View in PGS-Catalog
Target study
- Coverage: 6,369,007 (99.16%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000330
Reference score
- Variants: 6,437,380
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 898,130
- Population:
- Publication: Mars N et.al, Nat Med (2020-04-07)
- View in PGS-Catalog
Target study
- Coverage: 6,369,556 (98.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000331
Reference score
- Variants: 6,183,494
- Variants ignored: 0
-
Trait: Atrial fibrillation
- Mapped Trait(s):
- Samples: 1,030,836
- Population:
- Publication: Mars N et.al, Nat Med (2020-04-07)
- View in PGS-Catalog
Target study
- Coverage: 6,121,793 (99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000332
Reference score
- Variants: 6,390,808
- Variants ignored: 0
-
Trait: Breast cancer
- Mapped Trait(s):
- Samples: 139,274
- Population:
- Publication: Mars N et.al, Nat Med (2020-04-07)
- View in PGS-Catalog
Target study
- Coverage: 6,390,806 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000333
Reference score
- Variants: 6,606,785
- Variants ignored: 0
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 140,254
- Population:
- Publication: Mars N et.al, Nat Med (2020-04-07)
- View in PGS-Catalog
Target study
- Coverage: 6,605,914 (99.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000334
Reference score
- Variants: 22
- Variants ignored: 6
-
Trait: Late-onset Alzheimer’s disease
- Mapped Trait(s):
- Samples: 388,324
- Population:
- European: 80.9%
- Unknown: 19.1%
- Publication: Zhang Q et.al, Nat Commun (2020-09-23)
- View in PGS-Catalog
Target study
- Coverage: 16 (72.73%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000335
Reference score
- Variants: 1,079,089
- Variants ignored: 0
-
Trait: Breast cancer
- Mapped Trait(s):
- Samples: 139,274
- Population:
- Publication: Mars N et.al, Nat Commun (2020-12-14)
- View in PGS-Catalog
Target study
- Coverage: 1,078,706 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000336
Reference score
- Variants: 313
- Variants ignored: 54
-
Trait: Chronotype
- Mapped Trait(s):
- Samples: 403,195
- Population:
- Publication: Maukonen M et.al, J Biol Rhythms (2020-06-24)
- View in PGS-Catalog
Target study
- Coverage: 257 (82.11%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000338
Reference score
- Variants: 97
- Variants ignored: 20
-
Trait: Atrial fibrillation
- Mapped Trait(s):
- Samples: 588,190
- Population:
- European: 91.4%
- East Asian: 6.3%
- African: 1.5%
- Hispanic or Latin American: 0.9%
- Publication: Kloosterman M et.al, Eur J Heart Fail (2020-01-09)
- View in PGS-Catalog
Target study
- Coverage: 77 (79.38%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000339
Reference score
- Variants: 22
- Variants ignored: 0
-
Trait: Cutaneous melanoma
- Mapped Trait(s):
- Samples: 36,077
- Population:
- Publication: Law MH et.al, Hum Mol Genet (2020-10-01)
- View in PGS-Catalog
Target study
- Coverage: 22 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000340
Reference score
- Variants: 28
- Variants ignored: 0
-
Trait: Low-density lipoprotein cholesterol levels
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 94,595
- Population:
- Publication: Trinder M et.al, Circ Genom Precis Med (2020-08-13)
- View in PGS-Catalog
Target study
- Coverage: 0 (0%) zero
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000341
Reference score
- Variants: 33
- Variants ignored: 10
-
Trait: Systemic sclerosis
- Mapped Trait(s):
- Samples: 26,679
- Population:
- Publication: Bossini-Castillo L et.al, Ann Rheum Dis (2020-10-01)
- View in PGS-Catalog
Target study
- Coverage: 23 (69.7%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000342
Reference score
- Variants: 11
- Variants ignored: 45
-
Trait: Psoriatic arthritis
- Mapped Trait(s):
- Samples: 13,177
- Population:
- Publication: Smith MP et.al, J Psoriasis Psoriatic Arthritis (2020-03-04)
- View in PGS-Catalog
Target study
- Coverage: 6 (54.55%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000344
Reference score
- Variants: 287
- Variants ignored: 0
-
Trait: Breast cancer
- Mapped Trait(s):
- Samples: 139,274
- Population:
- Publication: Ho WK et.al, Nat Commun (2020-07-31)
- View in PGS-Catalog
Target study
- Coverage: 287 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000345
Reference score
- Variants: 229
- Variants ignored: 0
-
Trait: Breast cancer
- Mapped Trait(s):
- Samples: 139,274
- Population:
- Publication: Ho WK et.al, Nat Commun (2020-07-31)
- View in PGS-Catalog
Target study
- Coverage: 229 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000346
Reference score
- Variants: 287
- Variants ignored: 0
-
Trait: Estrogen receptor negative breast cancer
- Mapped Trait(s):
- Samples: 139,274
- Population:
- Publication: Ho WK et.al, Nat Commun (2020-07-31)
- View in PGS-Catalog
Target study
- Coverage: 287 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000347
Reference score
- Variants: 287
- Variants ignored: 0
-
Trait: Estrogen receptor positive breast cancer
- Mapped Trait(s):
- Samples: 139,274
- Population:
- Publication: Ho WK et.al, Nat Commun (2020-07-31)
- View in PGS-Catalog
Target study
- Coverage: 287 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000348
Reference score
- Variants: 72
- Variants ignored: 0
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 257,853
- Population:
- European: 88.9%
- African: 4.9%
- East Asian: 3.9%
- Hispanic or Latin American: 2.2%
- Publication: Black MH et.al, Prostate (2020-08-17)
- View in PGS-Catalog
Target study
- Coverage: 33 (45.83%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000349
Reference score
- Variants: 70
- Variants ignored: 0
-
Trait: Coronary artery disease
- Mapped Trait(s):
- Samples: 589,596
- Population:
- European: 59.2%
- Multi-Ancestry (including Europeans): 33%
- South Asian: 4.3%
- East Asian: 1.9%
- Hispanic or Latin American: 0.7%
- African: 0.5%
- Greater Middle Eastern: 0.4%
- Publication: Pechlivanis S et.al, BMC Med Genet (2020-09-10)
- View in PGS-Catalog
Target study
- Coverage: 69 (98.57%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000350
Reference score
- Variants: 12
- Variants ignored: 5
-
Trait: Primary open-angle glaucoma
- Mapped Trait(s):
- Samples: 122,995
- Population:
- European: 93.7%
- Multi-Ancestry (excluding Europeans): 6.3%
- Publication: Fan BJ et.al, JAMA Ophthalmol (2019-08-22)
- View in PGS-Catalog
Target study
- Coverage: 6 (50%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000351
Reference score
- Variants: 30
- Variants ignored: 0
-
Trait: Invasive epithelial ovarian cancer
- Mapped Trait(s):
- Samples: 322,760
- Population:
- Publication: Barnes DR et.al, Genet Med (2020-07-15)
- View in PGS-Catalog
Target study
- Coverage: 25 (83.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000352
Reference score
- Variants: 22
- Variants ignored: 0
-
Trait: High grade serous ovarian cancer
- Mapped Trait(s):
- Samples: 53,978
- Population:
- Publication: Barnes DR et.al, Genet Med (2020-07-15)
- View in PGS-Catalog
Target study
- Coverage: 19 (86.36%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000353
Reference score
- Variants: 14
- Variants ignored: 0
-
Trait: Any Cancer
- Mapped Trait(s):
- Samples: 371,216
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 14 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000354
Reference score
- Variants: 1,118,667
- Variants ignored: 0
-
Trait: Any Cancer
- Mapped Trait(s):
- Samples: 371,216
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,118,667 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000355
Reference score
- Variants: 15
- Variants ignored: 0
-
Trait: Any Cancer
- Mapped Trait(s):
- Samples: 371,216
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 15 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000356
Reference score
- Variants: 179
- Variants ignored: 0
-
Trait: Any Cancer
- Mapped Trait(s):
- Samples: 371,216
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 177 (98.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000357
Reference score
- Variants: 45
- Variants ignored: 0
-
Trait: Cancer of mouth
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 42 (93.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000358
Reference score
- Variants: 1,119,238
- Variants ignored: 0
-
Trait: Cancer of mouth
- Mapped Trait(s):
- Samples: 407,464
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,119,238 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000359
Reference score
- Variants: 931,954
- Variants ignored: 0
-
Trait: Cancer of tongue
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 931,954 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000360
Reference score
- Variants: 25,920
- Variants ignored: 0
-
Trait: Cancer of larynx
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 25,823 (99.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000361
Reference score
- Variants: 87,893
- Variants ignored: 0
-
Trait: Cancer of larynx
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 87,621 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000362
Reference score
- Variants: 53
- Variants ignored: 0
-
Trait: Cancer of larynx
- Mapped Trait(s):
- Samples: 407,079
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 53 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000363
Reference score
- Variants: 1,081,646
- Variants ignored: 0
-
Trait: Cancer of esophagus
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,081,646 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000364
Reference score
- Variants: 2,001
- Variants ignored: 0
-
Trait: Cancer of esophagus
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,996 (99.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000365
Reference score
- Variants: 1,070,434
- Variants ignored: 0
-
Trait: Cancer of esophagus
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,070,434 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000366
Reference score
- Variants: 1,119,238
- Variants ignored: 0
-
Trait: Cancer of esophagus
- Mapped Trait(s):
- Samples: 394,092
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,119,238 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000367
Reference score
- Variants: 74
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 63,920
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 74 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000368
Reference score
- Variants: 74
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 63,920
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 74 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000369
Reference score
- Variants: 81
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 63,920
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 80 (98.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000370
Reference score
- Variants: 87
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 63,920
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 86 (98.85%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000371
Reference score
- Variants: 18
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 122,140
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 18 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000372
Reference score
- Variants: 27
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 122,140
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 27 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000373
Reference score
- Variants: 1,119,238
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 387,318
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,119,238 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000374
Reference score
- Variants: 41
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 387,318
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 41 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000375
Reference score
- Variants: 370
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 387,318
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 368 (99.46%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000376
Reference score
- Variants: 1,111,490
- Variants ignored: 0
-
Trait: Colon cancer
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,111,490 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000377
Reference score
- Variants: 5,740,814
- Variants ignored: 0
-
Trait: Colon cancer
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 5,721,326 (99.66%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000378
Reference score
- Variants: 1,111,399
- Variants ignored: 0
-
Trait: Colon cancer
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,111,399 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000379
Reference score
- Variants: 5,715,093
- Variants ignored: 0
-
Trait: Colon cancer
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 5,695,668 (99.66%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000380
Reference score
- Variants: 1,119,238
- Variants ignored: 0
-
Trait: Colon cancer
- Mapped Trait(s):
- Samples: 385,807
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,119,238 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000381
Reference score
- Variants: 12
- Variants ignored: 0
-
Trait: Colon cancer
- Mapped Trait(s):
- Samples: 385,807
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 12 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000382
Reference score
- Variants: 150
- Variants ignored: 0
-
Trait: Colon cancer
- Mapped Trait(s):
- Samples: 385,807
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 150 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000383
Reference score
- Variants: 1,078,799
- Variants ignored: 0
-
Trait: Malignant neoplasm of rectum, rectosigmoid junction, and anus
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,078,799 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000384
Reference score
- Variants: 1,104,018
- Variants ignored: 0
-
Trait: Malignant neoplasm of rectum, rectosigmoid junction, and anus
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,104,018 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000385
Reference score
- Variants: 17
- Variants ignored: 0
-
Trait: Pancreatic cancer
- Mapped Trait(s):
- Samples: 46,491
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 17 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000386
Reference score
- Variants: 10
- Variants ignored: 0
-
Trait: Pancreatic cancer
- Mapped Trait(s):
- Samples: 46,491
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 10 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000387
Reference score
- Variants: 879,334
- Variants ignored: 0
-
Trait: Cancer within the respiratory system
- Mapped Trait(s):
- Samples: 408,926
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 874,379 (99.44%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000388
Reference score
- Variants: 1,109,069
- Variants ignored: 0
-
Trait: Cancer of bronchus; lung
- Mapped Trait(s):
- Samples: 1,083,582
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,109,069 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000389
Reference score
- Variants: 21
- Variants ignored: 0
-
Trait: Cancer of bronchus; lung
- Mapped Trait(s):
- Samples: 428,696
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 21 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000390
Reference score
- Variants: 21
- Variants ignored: 0
-
Trait: Cancer of bronchus; lung
- Mapped Trait(s):
- Samples: 428,696
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 21 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000391
Reference score
- Variants: 14
- Variants ignored: 0
-
Trait: Cancer of bronchus; lung
- Mapped Trait(s):
- Samples: 428,696
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 14 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000392
Reference score
- Variants: 19
- Variants ignored: 0
-
Trait: Cancer of bronchus; lung
- Mapped Trait(s):
- Samples: 428,696
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 19 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000393
Reference score
- Variants: 1,110,438
- Variants ignored: 0
-
Trait: Cancer of bronchus; lung
- Mapped Trait(s):
- Samples: 1,083,582
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,110,438 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000394
Reference score
- Variants: 1,110,438
- Variants ignored: 0
-
Trait: Cancer of bronchus; lung
- Mapped Trait(s):
- Samples: 1,083,582
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,110,438 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000395
Reference score
- Variants: 1,119,238
- Variants ignored: 0
-
Trait: Cancer of bronchus; lung
- Mapped Trait(s):
- Samples: 408,327
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,119,238 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000396
Reference score
- Variants: 75
- Variants ignored: 0
-
Trait: Cancer of bronchus; lung
- Mapped Trait(s):
- Samples: 408,327
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 74 (98.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000397
Reference score
- Variants: 46,920
- Variants ignored: 0
-
Trait: Cancer of bronchus; lung
- Mapped Trait(s):
- Samples: 408,327
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 46,323 (98.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000398
Reference score
- Variants: 1,103,220
- Variants ignored: 0
-
Trait: Skin cancer
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,103,220 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000399
Reference score
- Variants: 6
- Variants ignored: 0
-
Trait: Skin cancer
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 6 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000400
Reference score
- Variants: 95
- Variants ignored: 0
-
Trait: Skin cancer
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 91 (95.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000401
Reference score
- Variants: 1,111,490
- Variants ignored: 0
-
Trait: Skin cancer
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,111,490 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000402
Reference score
- Variants: 389
- Variants ignored: 0
-
Trait: Skin cancer
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 377 (96.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000403
Reference score
- Variants: 16,316
- Variants ignored: 0
-
Trait: Skin cancer
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 16,248 (99.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000404
Reference score
- Variants: 80
- Variants ignored: 0
-
Trait: Skin cancer
- Mapped Trait(s):
- Samples: 408,823
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 76 (95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000405
Reference score
- Variants: 1,119,238
- Variants ignored: 0
-
Trait: Skin cancer
- Mapped Trait(s):
- Samples: 408,823
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,119,238 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000406
Reference score
- Variants: 292
- Variants ignored: 0
-
Trait: Skin cancer
- Mapped Trait(s):
- Samples: 408,823
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 284 (97.26%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000407
Reference score
- Variants: 3,166
- Variants ignored: 0
-
Trait: Skin cancer
- Mapped Trait(s):
- Samples: 408,823
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 3,131 (98.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000408
Reference score
- Variants: 10
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 10 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000409
Reference score
- Variants: 1,111,490
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,111,490 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000410
Reference score
- Variants: 7
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 7 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000411
Reference score
- Variants: 185
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 182 (98.38%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000412
Reference score
- Variants: 16
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 16 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000413
Reference score
- Variants: 1,111,490
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,111,490 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000414
Reference score
- Variants: 21
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 21 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000415
Reference score
- Variants: 505
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 502 (99.41%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000416
Reference score
- Variants: 9
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 722,388
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 9 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000417
Reference score
- Variants: 1,109,519
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 722,388
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,109,519 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000418
Reference score
- Variants: 9
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 722,388
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 9 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000419
Reference score
- Variants: 436
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 722,388
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 434 (99.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000420
Reference score
- Variants: 147
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 722,388
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 145 (98.64%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000421
Reference score
- Variants: 18
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 356,564
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 18 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000422
Reference score
- Variants: 18
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 356,564
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 18 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000423
Reference score
- Variants: 29
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 356,564
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 28 (96.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000424
Reference score
- Variants: 27
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 356,564
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 26 (96.3%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000425
Reference score
- Variants: 20
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 294,219
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 20 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000426
Reference score
- Variants: 20
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 294,219
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 20 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000427
Reference score
- Variants: 20
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 294,219
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 20 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000428
Reference score
- Variants: 20
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 294,219
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 20 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000429
Reference score
- Variants: 12
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 397,762
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 12 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000430
Reference score
- Variants: 1,119,238
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 397,762
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,119,238 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000431
Reference score
- Variants: 15
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 397,762
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 15 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000432
Reference score
- Variants: 296
- Variants ignored: 0
-
Trait: Melanomas of skin (diagnosis or history)
- Mapped Trait(s):
- Samples: 397,762
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 292 (98.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000433
Reference score
- Variants: 108
- Variants ignored: 0
-
Trait: Other non-epithelial cancer of skin
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 102 (94.44%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000434
Reference score
- Variants: 1,111,490
- Variants ignored: 0
-
Trait: Other non-epithelial cancer of skin
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,111,490 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000435
Reference score
- Variants: 446
- Variants ignored: 0
-
Trait: Other non-epithelial cancer of skin
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 433 (97.09%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000436
Reference score
- Variants: 16,626
- Variants ignored: 0
-
Trait: Other non-epithelial cancer of skin
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 16,551 (99.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000437
Reference score
- Variants: 63
- Variants ignored: 0
-
Trait: Other non-epithelial cancer of skin
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 60 (95.24%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000438
Reference score
- Variants: 1,111,490
- Variants ignored: 0
-
Trait: Other non-epithelial cancer of skin
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,111,490 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000439
Reference score
- Variants: 467
- Variants ignored: 0
-
Trait: Other non-epithelial cancer of skin
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 454 (97.22%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000440
Reference score
- Variants: 2,111
- Variants ignored: 0
-
Trait: Other non-epithelial cancer of skin
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 2,098 (99.38%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000441
Reference score
- Variants: 77
- Variants ignored: 0
-
Trait: Other non-epithelial cancer of skin
- Mapped Trait(s):
- Samples: 406,220
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 74 (96.1%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000442
Reference score
- Variants: 1,119,238
- Variants ignored: 0
-
Trait: Other non-epithelial cancer of skin
- Mapped Trait(s):
- Samples: 406,220
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,119,238 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000443
Reference score
- Variants: 177
- Variants ignored: 0
-
Trait: Other non-epithelial cancer of skin
- Mapped Trait(s):
- Samples: 406,220
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 168 (94.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000444
Reference score
- Variants: 7,231
- Variants ignored: 0
-
Trait: Other non-epithelial cancer of skin
- Mapped Trait(s):
- Samples: 406,220
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 7,149 (98.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000445
Reference score
- Variants: 19
- Variants ignored: 0
-
Trait: Basal cell carcinoma
- Mapped Trait(s):
- Samples: 722,282
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 15 (78.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000446
Reference score
- Variants: 1,111,490
- Variants ignored: 0
-
Trait: Basal cell carcinoma
- Mapped Trait(s):
- Samples: 722,282
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,111,490 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000447
Reference score
- Variants: 72
- Variants ignored: 0
-
Trait: Basal cell carcinoma
- Mapped Trait(s):
- Samples: 722,282
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 68 (94.44%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000448
Reference score
- Variants: 183
- Variants ignored: 0
-
Trait: Basal cell carcinoma
- Mapped Trait(s):
- Samples: 722,282
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 179 (97.81%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000449
Reference score
- Variants: 1,073,162
- Variants ignored: 0
-
Trait: Basal cell carcinoma
- Mapped Trait(s):
- Samples: 722,282
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,073,162 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000450
Reference score
- Variants: 8
- Variants ignored: 0
-
Trait: Basal cell carcinoma
- Mapped Trait(s):
- Samples: 722,282
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 8 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000451
Reference score
- Variants: 2,231
- Variants ignored: 0
-
Trait: Basal cell carcinoma
- Mapped Trait(s):
- Samples: 722,282
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 2,224 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000452
Reference score
- Variants: 28
- Variants ignored: 0
-
Trait: Basal cell carcinoma
- Mapped Trait(s):
- Samples: 304,241
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 26 (92.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000453
Reference score
- Variants: 28
- Variants ignored: 0
-
Trait: Basal cell carcinoma
- Mapped Trait(s):
- Samples: 304,241
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 26 (92.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000454
Reference score
- Variants: 27
- Variants ignored: 0
-
Trait: Basal cell carcinoma
- Mapped Trait(s):
- Samples: 304,241
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 25 (92.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000455
Reference score
- Variants: 28
- Variants ignored: 0
-
Trait: Basal cell carcinoma
- Mapped Trait(s):
- Samples: 304,241
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 26 (92.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000456
Reference score
- Variants: 30
- Variants ignored: 0
-
Trait: Basal cell carcinoma
- Mapped Trait(s):
- Samples: 1,048,484
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 29 (96.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000457
Reference score
- Variants: 30
- Variants ignored: 0
-
Trait: Basal cell carcinoma
- Mapped Trait(s):
- Samples: 1,048,484
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 29 (96.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000458
Reference score
- Variants: 23
- Variants ignored: 0
-
Trait: Basal cell carcinoma
- Mapped Trait(s):
- Samples: 1,048,484
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 22 (95.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000459
Reference score
- Variants: 24
- Variants ignored: 0
-
Trait: Basal cell carcinoma
- Mapped Trait(s):
- Samples: 1,048,484
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 23 (95.83%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000460
Reference score
- Variants: 4,279,140
- Variants ignored: 0
-
Trait: Squamous cell carcinoma
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 4,264,940 (99.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000461
Reference score
- Variants: 13
- Variants ignored: 0
-
Trait: Squamous cell carcinoma
- Mapped Trait(s):
- Samples: 362,144
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 13 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000462
Reference score
- Variants: 13
- Variants ignored: 0
-
Trait: Squamous cell carcinoma
- Mapped Trait(s):
- Samples: 362,144
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 13 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000463
Reference score
- Variants: 7
- Variants ignored: 0
-
Trait: Squamous cell carcinoma
- Mapped Trait(s):
- Samples: 362,144
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 7 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000464
Reference score
- Variants: 14
- Variants ignored: 0
-
Trait: Squamous cell carcinoma
- Mapped Trait(s):
- Samples: 362,144
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 14 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000465
Reference score
- Variants: 10
- Variants ignored: 0
-
Trait: Squamous cell carcinoma
- Mapped Trait(s):
- Samples: 299,480
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 10 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000466
Reference score
- Variants: 10
- Variants ignored: 0
-
Trait: Squamous cell carcinoma
- Mapped Trait(s):
- Samples: 299,480
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 10 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000467
Reference score
- Variants: 6
- Variants ignored: 0
-
Trait: Squamous cell carcinoma
- Mapped Trait(s):
- Samples: 299,480
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 6 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000468
Reference score
- Variants: 9
- Variants ignored: 0
-
Trait: Squamous cell carcinoma
- Mapped Trait(s):
- Samples: 299,480
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 9 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000469
Reference score
- Variants: 1,119,238
- Variants ignored: 0
-
Trait: Carcinoma in situ of skin
- Mapped Trait(s):
- Samples: 395,738
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,119,238 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000470
Reference score
- Variants: 5
- Variants ignored: 0
-
Trait: Carcinoma in situ of skin
- Mapped Trait(s):
- Samples: 395,738
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 4 (80%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000471
Reference score
- Variants: 7
- Variants ignored: 0
-
Trait: Carcinoma in situ of skin
- Mapped Trait(s):
- Samples: 395,738
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 7 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000472
Reference score
- Variants: 22
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 194,153
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 22 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000473
Reference score
- Variants: 1,111,495
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 194,153
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,111,495 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000474
Reference score
- Variants: 68
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 194,153
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 67 (98.53%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000475
Reference score
- Variants: 30,041
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 194,153
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 29,942 (99.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000476
Reference score
- Variants: 32
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 194,174
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 32 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000477
Reference score
- Variants: 1,111,495
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 194,174
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,111,495 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000478
Reference score
- Variants: 120
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 194,174
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 119 (99.17%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000479
Reference score
- Variants: 2,267
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 194,174
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 2,259 (99.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000480
Reference score
- Variants: 20
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 388,348
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 20 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000481
Reference score
- Variants: 1,111,495
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 388,348
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,111,495 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000482
Reference score
- Variants: 42
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 388,348
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 42 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000483
Reference score
- Variants: 4,047
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 388,348
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 4,034 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000484
Reference score
- Variants: 25
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 388,348
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 24 (96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000485
Reference score
- Variants: 62
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 559,287
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 62 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000486
Reference score
- Variants: 86
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 559,287
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 86 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000487
Reference score
- Variants: 62
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 559,287
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 62 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000488
Reference score
- Variants: 79
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 559,287
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 79 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000489
Reference score
- Variants: 49
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 49 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000490
Reference score
- Variants: 49
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 49 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000491
Reference score
- Variants: 1,119,140
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,119,140 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000492
Reference score
- Variants: 1,120,410
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,120,410 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000493
Reference score
- Variants: 217
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 216 (99.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000494
Reference score
- Variants: 49
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 49 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000495
Reference score
- Variants: 18,866
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 18,866 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000496
Reference score
- Variants: 41,744
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 41,743 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000497
Reference score
- Variants: 257
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 257 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000498
Reference score
- Variants: 257
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 257 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000499
Reference score
- Variants: 1,119,140
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,119,140 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000500
Reference score
- Variants: 1,120,410
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,120,410 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000501
Reference score
- Variants: 1,142
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,134 (99.3%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000502
Reference score
- Variants: 747
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 741 (99.2%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000503
Reference score
- Variants: 61,635
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 61,635 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000504
Reference score
- Variants: 148,560
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 148,540 (99.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000505
Reference score
- Variants: 334
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 334 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000506
Reference score
- Variants: 334
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 334 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000507
Reference score
- Variants: 1,119,140
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,119,140 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000508
Reference score
- Variants: 1,120,410
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,120,410 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000509
Reference score
- Variants: 3,038
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 3,002 (98.82%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000510
Reference score
- Variants: 1,682
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,669 (99.23%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000511
Reference score
- Variants: 118,388
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 118,386 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000512
Reference score
- Variants: 286,144
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 286,107 (99.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000513
Reference score
- Variants: 41
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 213,515
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 41 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000514
Reference score
- Variants: 1,119,237
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 213,515
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,119,237 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000515
Reference score
- Variants: 84
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 213,515
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 83 (98.81%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000516
Reference score
- Variants: 6,977
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 213,515
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 6,925 (99.25%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000517
Reference score
- Variants: 10
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 10 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000518
Reference score
- Variants: 10
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 10 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000519
Reference score
- Variants: 1,115,376
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,115,376 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000520
Reference score
- Variants: 1,116,435
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,116,435 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000521
Reference score
- Variants: 9
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 9 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000522
Reference score
- Variants: 14
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 14 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000523
Reference score
- Variants: 270
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 270 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000524
Reference score
- Variants: 2,708
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 2,679 (98.93%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000525
Reference score
- Variants: 86
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 85 (98.84%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000526
Reference score
- Variants: 86
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 85 (98.84%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000527
Reference score
- Variants: 1,115,436
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,115,436 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000528
Reference score
- Variants: 1,116,495
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,116,495 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000529
Reference score
- Variants: 310
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 305 (98.39%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000530
Reference score
- Variants: 174
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 172 (98.85%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000531
Reference score
- Variants: 98,026
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 97,576 (99.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000532
Reference score
- Variants: 12,277
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 12,098 (98.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000533
Reference score
- Variants: 110
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 107 (97.27%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000534
Reference score
- Variants: 110
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 107 (97.27%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000535
Reference score
- Variants: 1,115,484
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,115,484 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000536
Reference score
- Variants: 1,116,546
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,116,546 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000537
Reference score
- Variants: 363
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 357 (98.35%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000538
Reference score
- Variants: 85
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 83 (97.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000539
Reference score
- Variants: 18,356
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 18,244 (99.39%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000540
Reference score
- Variants: 7,118
- Variants ignored: 0
-
Trait: Breast cancer (female)
- Mapped Trait(s):
- Samples: 1,063,736
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 7,011 (98.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000541
Reference score
- Variants: 18
- Variants ignored: 0
-
Trait: Malignant neoplasm of uterus
- Mapped Trait(s):
- Samples: 243,283
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 18 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000542
Reference score
- Variants: 20
- Variants ignored: 0
-
Trait: Malignant neoplasm of uterus
- Mapped Trait(s):
- Samples: 243,283
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 20 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000543
Reference score
- Variants: 8
- Variants ignored: 0
-
Trait: Cancer of other female genital organs
- Mapped Trait(s):
- Samples: 194,174
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 8 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000544
Reference score
- Variants: 21
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 512,028
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 21 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000545
Reference score
- Variants: 21
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 512,028
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 21 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000546
Reference score
- Variants: 1,115,189
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 314,752
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,115,189 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000547
Reference score
- Variants: 6
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 314,752
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 4 (66.67%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000548
Reference score
- Variants: 1,441
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 314,752
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,438 (99.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000549
Reference score
- Variants: 16
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 314,752
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 14 (87.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000550
Reference score
- Variants: 1,115,189
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 314,752
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,115,189 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000551
Reference score
- Variants: 12
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 314,752
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 10 (83.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000552
Reference score
- Variants: 41,269
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 314,752
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 41,257 (99.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000553
Reference score
- Variants: 10
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 314,752
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 9 (90%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000554
Reference score
- Variants: 1,115,189
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 314,752
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,115,189 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000555
Reference score
- Variants: 15
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 314,752
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 13 (86.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000556
Reference score
- Variants: 486,841
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 314,752
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 486,531 (99.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000557
Reference score
- Variants: 1,115,187
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 314,752
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,115,187 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000558
Reference score
- Variants: 1,098,236
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 314,752
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,097,138 (99.9%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000559
Reference score
- Variants: 21
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 314,752
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 19 (90.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000560
Reference score
- Variants: 21
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 314,752
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 19 (90.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000561
Reference score
- Variants: 1,114,056
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 314,752
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,114,056 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000562
Reference score
- Variants: 1,115,189
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 314,752
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,115,189 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000563
Reference score
- Variants: 12
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 314,752
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 10 (83.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000564
Reference score
- Variants: 110,710
- Variants ignored: 0
-
Trait: Malignant neoplasm of ovary
- Mapped Trait(s):
- Samples: 314,752
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 110,667 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000565
Reference score
- Variants: 21
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 166,988
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 21 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000566
Reference score
- Variants: 1,111,494
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 166,988
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,111,494 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000567
Reference score
- Variants: 78
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 166,988
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 77 (98.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000568
Reference score
- Variants: 1,401
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 166,988
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,398 (99.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000569
Reference score
- Variants: 49
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 167,020
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 48 (97.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000570
Reference score
- Variants: 1,111,493
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 167,020
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,111,493 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000571
Reference score
- Variants: 100
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 167,020
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 96 (96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000572
Reference score
- Variants: 1,809
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 167,020
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,808 (99.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000573
Reference score
- Variants: 31
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 167,020
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 31 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000574
Reference score
- Variants: 1,111,493
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 167,020
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,111,493 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000575
Reference score
- Variants: 47
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 167,020
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 45 (95.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000576
Reference score
- Variants: 905
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 167,020
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 904 (99.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000577
Reference score
- Variants: 117
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 644,688
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 111 (94.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000578
Reference score
- Variants: 117
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 644,688
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 111 (94.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000579
Reference score
- Variants: 122
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 644,688
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 116 (95.08%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000580
Reference score
- Variants: 118
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 644,688
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 112 (94.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000581
Reference score
- Variants: 377
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 140,254
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 362 (96.02%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000582
Reference score
- Variants: 377
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 140,254
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 362 (96.02%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000583
Reference score
- Variants: 1,119,311
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 140,254
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,119,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000584
Reference score
- Variants: 1,120,596
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 140,254
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,120,596 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000585
Reference score
- Variants: 1,301
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 140,254
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,246 (95.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000586
Reference score
- Variants: 1,023
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 140,254
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 980 (95.8%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000587
Reference score
- Variants: 26,418
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 140,254
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 26,399 (99.93%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000588
Reference score
- Variants: 178,259
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 140,254
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 178,175 (99.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000589
Reference score
- Variants: 42
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 175,928
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 42 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000590
Reference score
- Variants: 1,119,236
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 175,928
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,119,236 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000591
Reference score
- Variants: 80
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 175,928
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 79 (98.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000592
Reference score
- Variants: 1,334
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Samples: 175,928
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,323 (99.18%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000593
Reference score
- Variants: 45
- Variants ignored: 0
-
Trait: Cancer of other male genital organs
- Mapped Trait(s):
- Samples: 167,020
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 44 (97.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000594
Reference score
- Variants: 97
- Variants ignored: 0
-
Trait: Cancer of other male genital organs
- Mapped Trait(s):
- Samples: 167,020
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 93 (95.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000595
Reference score
- Variants: 9
- Variants ignored: 0
-
Trait: Malignant neoplasm of testis
- Mapped Trait(s):
- Samples: 166,988
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 7 (77.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000596
Reference score
- Variants: 5
- Variants ignored: 0
-
Trait: Malignant neoplasm of testis
- Mapped Trait(s):
- Samples: 166,988
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 5 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000597
Reference score
- Variants: 771
- Variants ignored: 0
-
Trait: Malignant neoplasm of testis
- Mapped Trait(s):
- Samples: 166,988
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 767 (99.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000598
Reference score
- Variants: 6
- Variants ignored: 0
-
Trait: Malignant neoplasm of testis
- Mapped Trait(s):
- Samples: 167,020
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 5 (83.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000599
Reference score
- Variants: 31
- Variants ignored: 0
-
Trait: Malignant neoplasm of testis
- Mapped Trait(s):
- Samples: 167,020
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 30 (96.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000600
Reference score
- Variants: 250
- Variants ignored: 0
-
Trait: Malignant neoplasm of testis
- Mapped Trait(s):
- Samples: 167,020
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 248 (99.2%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000601
Reference score
- Variants: 40
- Variants ignored: 0
-
Trait: Malignant neoplasm of testis
- Mapped Trait(s):
- Samples: 77,639
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 39 (97.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000602
Reference score
- Variants: 40
- Variants ignored: 0
-
Trait: Malignant neoplasm of testis
- Mapped Trait(s):
- Samples: 77,639
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 39 (97.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000603
Reference score
- Variants: 22
- Variants ignored: 0
-
Trait: Malignant neoplasm of testis
- Mapped Trait(s):
- Samples: 77,639
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 22 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000604
Reference score
- Variants: 44
- Variants ignored: 0
-
Trait: Malignant neoplasm of testis
- Mapped Trait(s):
- Samples: 77,639
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 43 (97.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000605
Reference score
- Variants: 12
- Variants ignored: 0
-
Trait: Malignant neoplasm of kidney, except pelvis
- Mapped Trait(s):
- Samples: 33,826
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 11 (91.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000606
Reference score
- Variants: 12
- Variants ignored: 0
-
Trait: Malignant neoplasm of kidney, except pelvis
- Mapped Trait(s):
- Samples: 33,826
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 11 (91.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000607
Reference score
- Variants: 1,095,241
- Variants ignored: 0
-
Trait: Cancer of bladder
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,095,241 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000608
Reference score
- Variants: 1,097,063
- Variants ignored: 0
-
Trait: Cancer of bladder
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,097,063 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000609
Reference score
- Variants: 1,130
- Variants ignored: 0
-
Trait: Cancer of bladder
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,126 (99.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000610
Reference score
- Variants: 13
- Variants ignored: 0
-
Trait: Cancer of bladder
- Mapped Trait(s):
- Samples: 248,538
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 13 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000611
Reference score
- Variants: 13
- Variants ignored: 0
-
Trait: Cancer of bladder
- Mapped Trait(s):
- Samples: 248,538
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 13 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000612
Reference score
- Variants: 13
- Variants ignored: 0
-
Trait: Cancer of bladder
- Mapped Trait(s):
- Samples: 248,538
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 13 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000613
Reference score
- Variants: 15
- Variants ignored: 0
-
Trait: Cancer of bladder
- Mapped Trait(s):
- Samples: 248,538
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 15 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000614
Reference score
- Variants: 1,119,238
- Variants ignored: 0
-
Trait: Cancer of bladder
- Mapped Trait(s):
- Samples: 407,223
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,119,238 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000615
Reference score
- Variants: 106
- Variants ignored: 0
-
Trait: Cancer of bladder
- Mapped Trait(s):
- Samples: 407,223
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 105 (99.06%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000616
Reference score
- Variants: 24,359
- Variants ignored: 0
-
Trait: Cancer of bladder
- Mapped Trait(s):
- Samples: 407,223
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 24,227 (99.46%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000617
Reference score
- Variants: 834,009
- Variants ignored: 0
-
Trait: Cancer of eye
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 834,009 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000618
Reference score
- Variants: 23
- Variants ignored: 0
-
Trait: Cancer of brain and nervous system
- Mapped Trait(s):
- Samples: 112,282
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 23 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000619
Reference score
- Variants: 19
- Variants ignored: 0
-
Trait: Cancer of brain and nervous system
- Mapped Trait(s):
- Samples: 112,282
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 19 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000620
Reference score
- Variants: 522
- Variants ignored: 0
-
Trait: Cancer of brain
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 521 (99.81%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000621
Reference score
- Variants: 12
- Variants ignored: 0
-
Trait: Cancer of brain
- Mapped Trait(s):
- Samples: 33,914
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 12 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000622
Reference score
- Variants: 12
- Variants ignored: 0
-
Trait: Cancer of brain
- Mapped Trait(s):
- Samples: 33,914
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 12 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000623
Reference score
- Variants: 11
- Variants ignored: 0
-
Trait: Cancer of brain
- Mapped Trait(s):
- Samples: 33,914
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 11 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000624
Reference score
- Variants: 5
- Variants ignored: 0
-
Trait: Cancer of brain
- Mapped Trait(s):
- Samples: 33,914
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 5 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000625
Reference score
- Variants: 11
- Variants ignored: 0
-
Trait: Cancer of brain
- Mapped Trait(s):
- Samples: 407,725
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 11 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000626
Reference score
- Variants: 8
- Variants ignored: 0
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 8 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000627
Reference score
- Variants: 11
- Variants ignored: 0
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 11 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000628
Reference score
- Variants: 656
- Variants ignored: 0
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 654 (99.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000629
Reference score
- Variants: 8
- Variants ignored: 0
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 8 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000630
Reference score
- Variants: 10
- Variants ignored: 0
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Samples: 357,784
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 10 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000631
Reference score
- Variants: 10
- Variants ignored: 0
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Samples: 357,784
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 10 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000632
Reference score
- Variants: 8
- Variants ignored: 0
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Samples: 357,784
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 8 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000633
Reference score
- Variants: 5
- Variants ignored: 0
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Samples: 357,784
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 5 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000634
Reference score
- Variants: 1,119,238
- Variants ignored: 0
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Samples: 407,757
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,119,238 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000635
Reference score
- Variants: 5
- Variants ignored: 0
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Samples: 407,757
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 5 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000636
Reference score
- Variants: 954
- Variants ignored: 0
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Samples: 407,757
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 945 (99.06%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000637
Reference score
- Variants: 1,047,511
- Variants ignored: 0
-
Trait: Hodgkin's disease
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,047,511 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000638
Reference score
- Variants: 16
- Variants ignored: 0
-
Trait: Hodgkin's disease
- Mapped Trait(s):
- Samples: 83,473
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 16 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000639
Reference score
- Variants: 20
- Variants ignored: 0
-
Trait: Hodgkin's disease
- Mapped Trait(s):
- Samples: 83,473
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 20 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000640
Reference score
- Variants: 1,119,335
- Variants ignored: 0
-
Trait: Hodgkin's disease
- Mapped Trait(s):
- Samples: 404,724
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,111,172 (99.27%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000641
Reference score
- Variants: 12
- Variants ignored: 0
-
Trait: Non-Hodgkins lymphoma
- Mapped Trait(s):
- Samples: 25,391
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 12 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000642
Reference score
- Variants: 10
- Variants ignored: 0
-
Trait: Non-Hodgkins lymphoma
- Mapped Trait(s):
- Samples: 25,391
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 10 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000643
Reference score
- Variants: 1,048,780
- Variants ignored: 0
-
Trait: Nodular lymphoma
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 1,048,780 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000644
Reference score
- Variants: 2,209,179
- Variants ignored: 0
-
Trait: Nodular lymphoma
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 2,201,948 (99.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000645
Reference score
- Variants: 6
- Variants ignored: 0
-
Trait: Lymphoid leukemia
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 5 (83.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000646
Reference score
- Variants: 32
- Variants ignored: 0
-
Trait: Lymphoid leukemia, chronic
- Mapped Trait(s):
- Samples: 51,308
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 32 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000647
Reference score
- Variants: 32
- Variants ignored: 0
-
Trait: Lymphoid leukemia, chronic
- Mapped Trait(s):
- Samples: 51,308
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 32 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000648
Reference score
- Variants: 44
- Variants ignored: 0
-
Trait: Lymphoid leukemia, chronic
- Mapped Trait(s):
- Samples: 51,308
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 44 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000649
Reference score
- Variants: 27
- Variants ignored: 0
-
Trait: Lymphoid leukemia, chronic
- Mapped Trait(s):
- Samples: 51,308
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 27 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000650
Reference score
- Variants: 6
- Variants ignored: 0
-
Trait: Lymphoid leukemia, chronic
- Mapped Trait(s):
- Samples: 404,972
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 6 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000651
Reference score
- Variants: 76
- Variants ignored: 0
-
Trait: Lymphoid leukemia, chronic
- Mapped Trait(s):
- Samples: 404,972
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 76 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000652
Reference score
- Variants: 27
- Variants ignored: 0
-
Trait: Multiple myeloma
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 25 (92.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000653
Reference score
- Variants: 22
- Variants ignored: 0
-
Trait: Multiple myeloma
- Mapped Trait(s):
- Samples: 1,048,104
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 22 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000654
Reference score
- Variants: 21
- Variants ignored: 0
-
Trait: Multiple myeloma
- Mapped Trait(s):
- Samples: 1,048,104
- Population:
- Publication: Fritsche LG et.al, Am J Hum Genet (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 21 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000655
Reference score
- Variants: 10
- Variants ignored: 2
-
Trait: Non-alcoholic fatty liver disease
- Mapped Trait(s):
- Samples: 9,677
- Population:
- Publication: Namjou B et.al, BMC Med (2019-07-17)
- View in PGS-Catalog
Target study
- Coverage: 8 (80%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000656
Reference score
- Variants: 11
- Variants ignored: 2
-
Trait: Non-alcoholic fatty liver disease activity score
- Mapped Trait(s):
- EFO_0008421: non-alcoholic fatty liver disease severity measurement
- Samples: 235
- Population:
- Publication: Namjou B et.al, BMC Med (2019-07-17)
- View in PGS-Catalog
Target study
- Coverage: 9 (81.82%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000657
Reference score
- Variants: 21,716
- Variants ignored: 0
-
Trait: Heel quantitative ultrasound speed of sound (SOS)
- Mapped Trait(s):
- EFO_0007772: calcaneal bone quantitative ultrasound measurement
- Publication: Forgetta V et.al, PLoS Med (2020-07-02)
- View in PGS-Catalog
Target study
- Coverage: 0 (0%) zero
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000658
Reference score
- Variants: 229
- Variants ignored: 0
-
Trait: Total cholesterol
- Mapped Trait(s):
- Samples: 128,305
- Population:
- Publication: Tam CHT et.al, Genome Med (2021-02-19)
- View in PGS-Catalog
Target study
- Coverage: 229 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000659
Reference score
- Variants: 142
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 105,597
- Population:
- Publication: Tam CHT et.al, Genome Med (2021-02-19)
- View in PGS-Catalog
Target study
- Coverage: 142 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000660
Reference score
- Variants: 549
- Variants ignored: 0
-
Trait: HDL cholesterol
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 70,657
- Population:
- Publication: Tam CHT et.al, Genome Med (2021-02-19)
- View in PGS-Catalog
Target study
- Coverage: 549 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000661
Reference score
- Variants: 84
- Variants ignored: 0
-
Trait: LDL cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 72,866
- Population:
- Publication: Tam CHT et.al, Genome Med (2021-02-19)
- View in PGS-Catalog
Target study
- Coverage: 84 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000662
Reference score
- Variants: 269
- Variants ignored: 0
-
Trait: Prostate Cancer
- Mapped Trait(s):
- Samples: 234,253
- Population:
- European: 75.8%
- East Asian: 11.7%
- Multi-Ancestry (excluding Europeans): 9.1%
- Hispanic or Latin American: 3.4%
- Publication: Conti DV et.al, Nat Genet (2021-01-04)
- View in PGS-Catalog
Target study
- Coverage: 260 (96.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000663
Reference score
- Variants: 22
- Variants ignored: 0
-
Trait: Pancreatic cancer
- Mapped Trait(s):
- Samples: 57,275
- Population:
- European: 86.6%
- Unknown: 12.3%
- Multi-Ancestry (excluding Europeans): 1.1%
- Publication: Kim J et.al, Cancer Epidemiol Biomarkers Prev (2020-04-22)
- View in PGS-Catalog
Target study
- Coverage: 21 (95.45%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000664
Reference score
- Variants: 7
- Variants ignored: 0
-
Trait: Rapid decline of glomerular filtration rate (GFR)
- Mapped Trait(s):
- Samples: 1,102,457
- Population:
- European: 51.5%
- Multi-Ancestry (including Europeans): 30.6%
- East Asian: 15%
- African: 1.3%
- South Asian: 1.2%
- Hispanic or Latin American: 0.4%
- Publication: Gorski M et.al, Kidney Int (2020-10-30)
- View in PGS-Catalog
Target study
- Coverage: 7 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000665
Reference score
- Variants: 32
- Variants ignored: 0
-
Trait: Ischemic stroke
- Mapped Trait(s):
- Samples: 524,354
- Population:
- European: 85.2%
- East Asian: 8.7%
- African: 3.9%
- South Asian: 1.7%
- Hispanic or Latin American: 0.3%
- Additional Asian Ancestries: 0.1%
- Publication: Marston NA et.al, Circulation (2020-11-13)
- View in PGS-Catalog
Target study
- Coverage: 0 (0%) zero
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000666
Reference score
- Variants: 28
- Variants ignored: 0
-
Trait: Body surface area-indexed left ventricular end-systolic volume
- Mapped Trait(s):
- EFO_0008206: left ventricular systolic function measurement
- Samples: 36,041
- Population:
- European: 98.2%
- South Asian: 0.8%
- Unknown: 0.4%
- East Asian: 0.3%
- African: 0.3%
- Publication: Pirruccello JP et.al, Nat Commun (2020-05-07)
- View in PGS-Catalog
Target study
- Coverage: 28 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000667
Reference score
- Variants: 43
- Variants ignored: 0
-
Trait: Lipoprotein A
- Mapped Trait(s):
- Samples: 48,333
- Population:
- Publication: Trinder M et.al, JAMA Cardiol (2020-10-06)
- View in PGS-Catalog
Target study
- Coverage: 39 (90.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000668
Reference score
- Variants: 12,076
- Variants ignored: 0
-
Trait: Alanine aminotransferase [U/L]
- Mapped Trait(s):
- EFO_0004735: serum alanine aminotransferase measurement
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 11,495 (95.19%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000669
Reference score
- Variants: 11,912
- Variants ignored: 0
-
Trait: Albumin [g/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 11,372 (95.47%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000670
Reference score
- Variants: 18,328
- Variants ignored: 0
-
Trait: Alkaline phosphatase [U/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 17,492 (95.44%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000671
Reference score
- Variants: 19,324
- Variants ignored: 0
-
Trait: Apolipoprotein A [g/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 18,442 (95.44%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000672
Reference score
- Variants: 18,666
- Variants ignored: 0
-
Trait: Apolipoprotein B [g/L] (statin adjusted)
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 17,787 (95.29%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000673
Reference score
- Variants: 12,829
- Variants ignored: 0
-
Trait: Aspartate aminotransferase [U/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 12,172 (94.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000674
Reference score
- Variants: 15,548
- Variants ignored: 0
-
Trait: AST to ALT ratio
- Mapped Trait(s):
- EFO_0010934: aspartate aminotransferase to alanine aminotransferase ratio
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 14,796 (95.16%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000675
Reference score
- Variants: 17,378
- Variants ignored: 0
-
Trait: C-reactive protein [mg/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 16,538 (95.17%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000676
Reference score
- Variants: 12,334
- Variants ignored: 0
-
Trait: Calcium [mmol/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 11,692 (94.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000677
Reference score
- Variants: 17,204
- Variants ignored: 0
-
Trait: Cholesterol [mmol/L] (statin adjusted)
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 16,376 (95.19%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000678
Reference score
- Variants: 21,027
- Variants ignored: 0
-
Trait: Creatinine [umol/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 20,056 (95.38%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000679
Reference score
- Variants: 5,469
- Variants ignored: 0
-
Trait: Creatinine in urine [umol/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 5,137 (93.93%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000680
Reference score
- Variants: 24,487
- Variants ignored: 0
-
Trait: Cystatin C [mg/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 23,331 (95.28%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000681
Reference score
- Variants: 3,104
- Variants ignored: 0
-
Trait: Direct bilirubin [umol/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 2,902 (93.49%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000682
Reference score
- Variants: 17,467
- Variants ignored: 0
-
Trait: eGFR [ml/min/1.73m2]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 16,603 (95.05%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000683
Reference score
- Variants: 17,323
- Variants ignored: 0
-
Trait: Gamma glutamyltransferase [U/L]
- Mapped Trait(s):
- EFO_0004532: serum gamma-glutamyl transferase measurement
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 16,491 (95.2%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000684
Reference score
- Variants: 3,313
- Variants ignored: 0
-
Trait: Glucose [mmol/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 3,066 (92.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000685
Reference score
- Variants: 14,658
- Variants ignored: 0
-
Trait: HbA1c [mmol/mol]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 13,888 (94.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000686
Reference score
- Variants: 25,069
- Variants ignored: 0
-
Trait: HDL cholesterol [mmol/L]
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 23,914 (95.39%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000687
Reference score
- Variants: 23,443
- Variants ignored: 0
-
Trait: IGF-1 [nmol/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 22,354 (95.35%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000688
Reference score
- Variants: 16,184
- Variants ignored: 0
-
Trait: LDL cholesterol [mmol/L] (statin adjusted)
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 15,428 (95.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000689
Reference score
- Variants: 8,308
- Variants ignored: 0
-
Trait: Lipoprotein A [nmol/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 7,851 (94.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000690
Reference score
- Variants: 111
- Variants ignored: 0
-
Trait: Microalbumin in urine [mg/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 87 (78.38%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000691
Reference score
- Variants: 18,670
- Variants ignored: 0
-
Trait: Non-albumin protein [g/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 17,820 (95.45%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000692
Reference score
- Variants: 12,448
- Variants ignored: 0
-
Trait: Phosphate [mmol/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 11,808 (94.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000693
Reference score
- Variants: 2,423
- Variants ignored: 0
-
Trait: Potassium in urine [mmol/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 2,256 (93.11%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000694
Reference score
- Variants: 19,328
- Variants ignored: 0
-
Trait: SHBG [nmol/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 18,481 (95.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000695
Reference score
- Variants: 5,833
- Variants ignored: 0
-
Trait: Sodium in urine [mmol/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 5,478 (93.91%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000696
Reference score
- Variants: 8,223
- Variants ignored: 0
-
Trait: Testosterone [nmol/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 7,804 (94.9%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000697
Reference score
- Variants: 1,159
- Variants ignored: 0
-
Trait: Total bilirubin [umol/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 1,089 (93.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000698
Reference score
- Variants: 16,420
- Variants ignored: 0
-
Trait: Total protein [g/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 15,668 (95.42%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000699
Reference score
- Variants: 16,003
- Variants ignored: 0
-
Trait: Triglycerides [mmol/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 15,210 (95.04%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000700
Reference score
- Variants: 20,171
- Variants ignored: 0
-
Trait: Urate [umol/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 19,222 (95.3%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000701
Reference score
- Variants: 12,351
- Variants ignored: 0
-
Trait: Urea [mmol/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 11,700 (94.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000702
Reference score
- Variants: 8,012
- Variants ignored: 0
-
Trait: Vitamin D [nmol/L]
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 7,633 (95.27%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000703
Reference score
- Variants: 183,692
- Variants ignored: 0
-
Trait: Angina
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 175,884 (95.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000704
Reference score
- Variants: 183,271
- Variants ignored: 0
-
Trait: Alcoholic cirrhosis
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 175,486 (95.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000705
Reference score
- Variants: 183,458
- Variants ignored: 0
-
Trait: Gallstones
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 175,665 (95.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000706
Reference score
- Variants: 186,726
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 178,826 (95.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000707
Reference score
- Variants: 183,329
- Variants ignored: 0
-
Trait: Cholecystitis
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 175,541 (95.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000708
Reference score
- Variants: 183,272
- Variants ignored: 0
-
Trait: Kidney failure
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 175,487 (95.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000709
Reference score
- Variants: 183,287
- Variants ignored: 0
-
Trait: Heart failure
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 175,501 (95.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000710
Reference score
- Variants: 183,566
- Variants ignored: 0
-
Trait: Myocardial infarction
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 175,758 (95.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000711
Reference score
- Variants: 183,332
- Variants ignored: 0
-
Trait: Gout
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 175,540 (95.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000712
Reference score
- Variants: 183,695
- Variants ignored: 0
-
Trait: T2D (cases vs HbA1c filtered controls)
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 175,883 (95.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000713
Reference score
- Variants: 183,830
- Variants ignored: 0
-
Trait: T2D
- Mapped Trait(s):
- Publication: Sinnott-Armstrong N et.al, Nat Genet (2021-01-18)
- View in PGS-Catalog
Target study
- Coverage: 176,006 (95.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000714
Reference score
- Variants: 55
- Variants ignored: 0
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 22,548
- Population:
- Publication: Sipeky C et.al, Sci Rep (2020-10-13)
- View in PGS-Catalog
Target study
- Coverage: 33 (60%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000716
Reference score
- Variants: 295
- Variants ignored: 0
-
Trait: Early life body size
- Mapped Trait(s):
- Samples: 453,169
- Population:
- Publication: Richardson TG et.al, BMJ (2020-05-06)
- View in PGS-Catalog
Target study
- Coverage: 295 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000717
Reference score
- Variants: 557
- Variants ignored: 0
-
Trait: Adult life body size
- Mapped Trait(s):
- Samples: 453,169
- Population:
- Publication: Richardson TG et.al, BMJ (2020-05-06)
- View in PGS-Catalog
Target study
- Coverage: 557 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000718
Reference score
- Variants: 44
- Variants ignored: 0
-
Trait: Beta-blocker survival benefit
- Mapped Trait(s):
- Samples: 248
- Population:
- Publication: Lanfear DE et.al, Circ Heart Fail (2020-10-04)
- View in PGS-Catalog
Target study
- Coverage: 44 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000719
Reference score
- Variants: 134
- Variants ignored: 26
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 140,254
- Population:
- Publication: Jia G et.al, JNCI Cancer Spectr (2020-03-12)
- View in PGS-Catalog
Target study
- Coverage: 103 (76.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000720
Reference score
- Variants: 95
- Variants ignored: 19
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 74,409
- Population:
- European: 91.1%
- African: 8.9%
- Publication: Jia G et.al, JNCI Cancer Spectr (2020-03-12)
- View in PGS-Catalog
Target study
- Coverage: 76 (80%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000721
Reference score
- Variants: 19
- Variants ignored: 5
-
Trait: Lung cancer
- Mapped Trait(s):
- Samples: 293,065
- Population:
- Publication: Jia G et.al, JNCI Cancer Spectr (2020-03-12)
- View in PGS-Catalog
Target study
- Coverage: 14 (73.68%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000722
Reference score
- Variants: 15
- Variants ignored: 3
-
Trait: Kidney cancer
- Mapped Trait(s):
- Samples: 142,756
- Population:
- Publication: Jia G et.al, JNCI Cancer Spectr (2020-03-12)
- View in PGS-Catalog
Target study
- Coverage: 12 (80%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000723
Reference score
- Variants: 14
- Variants ignored: 2
-
Trait: Bladder cancer
- Mapped Trait(s):
- Samples: 455,744
- Population:
- Publication: Jia G et.al, JNCI Cancer Spectr (2020-03-12)
- View in PGS-Catalog
Target study
- Coverage: 12 (85.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000724
Reference score
- Variants: 31
- Variants ignored: 7
-
Trait: Epithelial ovarian cancer
- Mapped Trait(s):
- Samples: 85,426
- Population:
- Publication: Jia G et.al, JNCI Cancer Spectr (2020-03-12)
- View in PGS-Catalog
Target study
- Coverage: 24 (77.42%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000725
Reference score
- Variants: 22
- Variants ignored: 3
-
Trait: Pancreatic cancer
- Mapped Trait(s):
- Samples: 21,536
- Population:
- Publication: Jia G et.al, JNCI Cancer Spectr (2020-03-12)
- View in PGS-Catalog
Target study
- Coverage: 19 (86.36%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000726
Reference score
- Variants: 12
- Variants ignored: 0
-
Trait: Cirrhosis
- Mapped Trait(s):
- Samples: 440,073
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Emdin CA et.al, Gastroenterology (2020-12-10)
- View in PGS-Catalog
Target study
- Coverage: 12 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000727
Reference score
- Variants: 2,210,336
- Variants ignored: 0
-
Trait: Atrial fibrillation
- Mapped Trait(s):
- Samples: 1,030,836
- Population:
- Publication: Ritchie SC et.al, Nat Metab (2021-11-08)
- View in PGS-Catalog
Target study
- Coverage: 2,186,424 (98.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000728
Reference score
- Variants: 1,958,860
- Variants ignored: 0
-
Trait: Chronic kidney disease
- Mapped Trait(s):
- Samples: 625,219
- Population:
- Publication: Ritchie SC et.al, Nat Metab (2021-11-08)
- View in PGS-Catalog
Target study
- Coverage: 1,953,582 (99.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000729
Reference score
- Variants: 2,017,388
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 298,957
- Population:
- Publication: Ritchie SC et.al, Nat Metab (2021-11-08)
- View in PGS-Catalog
Target study
- Coverage: 1,999,128 (99.09%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000730
Reference score
- Variants: 47
- Variants ignored: 0
-
Trait: Basal cell carcinoma
- Mapped Trait(s):
- Samples: 103,008
- Population:
- Publication: Fontanillas P et.al, Nat Commun (2021-01-08)
- View in PGS-Catalog
Target study
- Coverage: 41 (87.23%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000731
Reference score
- Variants: 14
- Variants ignored: 0
-
Trait: Squamous cell carcinoma
- Mapped Trait(s):
- Samples: 103,008
- Population:
- Publication: Fontanillas P et.al, Nat Commun (2021-01-08)
- View in PGS-Catalog
Target study
- Coverage: 12 (85.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000732
Reference score
- Variants: 18
- Variants ignored: 0
-
Trait: Melanoma
- Mapped Trait(s):
- Samples: 103,008
- Population:
- Publication: Fontanillas P et.al, Nat Commun (2021-01-08)
- View in PGS-Catalog
Target study
- Coverage: 15 (83.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000733
Reference score
- Variants: 49
- Variants ignored: 0
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 31,747
- Population:
- Publication: Karunamuni RA et.al, Int J Cancer (2020-09-24)
- View in PGS-Catalog
Target study
- Coverage: 23 (46.94%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000734
Reference score
- Variants: 95
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 125,478
- Population:
- European: 95.8%
- East Asian: 4.2%
- Publication: Archambault AN et.al, Gastroenterology (2019-12-19)
- View in PGS-Catalog
Target study
- Coverage: 93 (97.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000735
Reference score
- Variants: 44
- Variants ignored: 0
-
Trait: PR interval
- Mapped Trait(s):
- Samples: 92,340
- Population:
- Publication: Tadros R et.al, Eur Heart J (2019-10-01)
- View in PGS-Catalog
Target study
- Coverage: 44 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000736
Reference score
- Variants: 26
- Variants ignored: 0
-
Trait: QRS duration
- Mapped Trait(s):
- Samples: 60,255
- Population:
- Publication: Tadros R et.al, Eur Heart J (2019-10-01)
- View in PGS-Catalog
Target study
- Coverage: 26 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000737
Reference score
- Variants: 3
- Variants ignored: 0
-
Trait: Brugada syndrome
- Mapped Trait(s):
- Samples: 1,427
- Population:
- Publication: Tadros R et.al, Eur Heart J (2019-10-01)
- View in PGS-Catalog
Target study
- Coverage: 3 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000738
Reference score
- Variants: 48
- Variants ignored: 0
-
Trait: Vitiligo
- Mapped Trait(s):
- Samples: 40,258
- Population:
- Publication: Roberts GHL et.al, Am J Hum Genet (2019-07-18)
- View in PGS-Catalog
Target study
- Coverage: 46 (95.83%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000739
Reference score
- Variants: 27
- Variants ignored: 0
-
Trait: Hypertrophic cardiomyopathy
- Mapped Trait(s):
- Samples: 50,266
- Population:
- European: 89.7%
- South Asian: 3.7%
- African: 3.1%
- Unknown: 2.1%
- East Asian: 0.8%
- Additional Diverse Ancestries: 0.6%
- Publication: Harper AR et.al, Nat Genet (2021-01-25)
- View in PGS-Catalog
Target study
- Coverage: 25 (92.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000740
Reference score
- Variants: 128
- Variants ignored: 0
-
Trait: Lung cancer
- Mapped Trait(s):
- Samples: 308,645
- Population:
- Publication: Hung RJ et.al, Cancer Res (2021-01-20)
- View in PGS-Catalog
Target study
- Coverage: 123 (96.09%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000741
Reference score
- Variants: 46
- Variants ignored: 0
-
Trait: Prostate cancer
- Mapped Trait(s):
- Publication: Huynh-Le MP et.al, Nat Commun (2021-02-23)
- View in PGS-Catalog
Target study
- Coverage: 22 (47.83%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000742
Reference score
- Variants: 166
- Variants ignored: 0
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 172,001
- Population:
- Publication: Karunamuni RA et.al, Prostate Cancer Prostatic Dis (2021-01-08)
- View in PGS-Catalog
Target study
- Coverage: 159 (95.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000743
Reference score
- Variants: 45
- Variants ignored: 0
-
Trait: Melanoma
- Mapped Trait(s):
- Samples: 36,077
- Population:
- Publication: Cust AE et.al, J Invest Dermatol (2018-06-08)
- View in PGS-Catalog
Target study
- Coverage: 43 (95.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000744
Reference score
- Variants: 31
- Variants ignored: 0
-
Trait: Melanoma
- Mapped Trait(s):
- Samples: 36,077
- Population:
- Publication: Cust AE et.al, J Invest Dermatol (2018-06-08)
- View in PGS-Catalog
Target study
- Coverage: 30 (96.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000745
Reference score
- Variants: 9
- Variants ignored: 0
-
Trait: Melanoma
- Mapped Trait(s):
- Samples: 36,077
- Population:
- Publication: Cust AE et.al, J Invest Dermatol (2018-06-08)
- View in PGS-Catalog
Target study
- Coverage: 8 (88.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000746
Reference score
- Variants: 1,940
- Variants ignored: 0
-
Trait: Coronary artery disease
- Mapped Trait(s):
- Samples: 187,599
- Population:
- European: 75.3%
- South Asian: 13.6%
- East Asian: 6%
- Hispanic or Latin American: 2.2%
- African: 1.7%
- Greater Middle Eastern: 1.2%
- Publication: Gola D et.al, Circ Genom Precis Med (2020-11-10)
- View in PGS-Catalog
Target study
- Coverage: 1,940 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000747
Reference score
- Variants: 375,822
- Variants ignored: 0
-
Trait: Coronary artery disease
- Mapped Trait(s):
- Samples: 187,599
- Population:
- European: 75.3%
- South Asian: 13.6%
- East Asian: 6%
- Hispanic or Latin American: 2.2%
- African: 1.7%
- Greater Middle Eastern: 1.2%
- Publication: Gola D et.al, Circ Genom Precis Med (2020-11-10)
- View in PGS-Catalog
Target study
- Coverage: 375,818 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000748
Reference score
- Variants: 3,423,987
- Variants ignored: 0
-
Trait: Coronary artery disease
- Mapped Trait(s):
- Samples: 187,599
- Population:
- European: 75.3%
- South Asian: 13.6%
- East Asian: 6%
- Hispanic or Latin American: 2.2%
- African: 1.7%
- Greater Middle Eastern: 1.2%
- Publication: Gola D et.al, Circ Genom Precis Med (2020-11-10)
- View in PGS-Catalog
Target study
- Coverage: 3,416,440 (99.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000749
Reference score
- Variants: 1,056,021
- Variants ignored: 0
-
Trait: Coronary artery disease
- Mapped Trait(s):
- Samples: 187,599
- Population:
- European: 75.3%
- South Asian: 13.6%
- East Asian: 6%
- Hispanic or Latin American: 2.2%
- African: 1.7%
- Greater Middle Eastern: 1.2%
- Publication: Gola D et.al, Circ Genom Precis Med (2020-11-10)
- View in PGS-Catalog
Target study
- Coverage: 1,053,758 (99.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000750
Reference score
- Variants: 43
- Variants ignored: 0
-
Trait: Parkinson's disease
- Mapped Trait(s):
- Samples: 417,508
- Population:
- Publication: Bobbili DR et.al, J Med Genet (2020-02-13)
- View in PGS-Catalog
Target study
- Coverage: 43 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000751
Reference score
- Variants: 178
- Variants ignored: 36
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 436,934
- Population:
- European: 93.5%
- African: 2.9%
- Multi-Ancestry (excluding Europeans): 1.9%
- East Asian: 1.7%
- Publication: Du Z et.al, Int J Cancer (2019-07-03)
- View in PGS-Catalog
Target study
- Coverage: 118 (66.29%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000752
Reference score
- Variants: 11,446
- Variants ignored: 0
-
Trait: Lipoprotein(a) concentration [nmol/L]
- Mapped Trait(s):
- Samples: 258,775
- Population:
- Publication: Dron JS et.al, Circ Genom Precis Med (2021-02-01)
- View in PGS-Catalog
Target study
- Coverage: 11,428 (99.84%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000753
Reference score
- Variants: 29
- Variants ignored: 0
-
Trait: Abdominal aortic aneurysm
- Mapped Trait(s):
- Samples: 179,814
- Population:
- Publication: Klarin D et.al, Circulation (2020-09-28)
- View in PGS-Catalog
Target study
- Coverage: 29 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000754
Reference score
- Variants: 293,684
- Variants ignored: 0
-
Trait: Systemic lupus erythrmatosus
- Mapped Trait(s):
- Samples: 10,064
- Population:
- Publication: Wang YF et.al, Nat Commun (2021-02-03)
- View in PGS-Catalog
Target study
- Coverage: 293,684 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000755
Reference score
- Variants: 14
- Variants ignored: 2
-
Trait: Serum uric acid levels
- Mapped Trait(s):
- Samples: 6,881
- Population:
- Publication: Cho SK et.al, Sci Rep (2020-06-08)
- View in PGS-Catalog
Target study
- Coverage: 12 (85.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000756
Reference score
- Variants: 32
- Variants ignored: 0
-
Trait: Narcolepsy
- Mapped Trait(s):
- Samples: 27,019
- Population:
- European: 61.9%
- East Asian: 38.1%
- Publication: Ouyang H et.al, Ann Transl Med (2020-02-01)
- View in PGS-Catalog
Target study
- Coverage: 31 (96.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000757
Reference score
- Variants: 5
- Variants ignored: 0
-
Trait: Narcolepsy
- Mapped Trait(s):
- Samples: 10,303
- Population:
- Publication: Ouyang H et.al, Ann Transl Med (2020-02-01)
- View in PGS-Catalog
Target study
- Coverage: 4 (80%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000758
Reference score
- Variants: 33,938
- Variants ignored: 0
-
Trait: Adult standing height
- Mapped Trait(s):
- Samples: 607,346
- Population:
- Publication: Lu T et.al, J Clin Endocrinol Metab (2021-03-31)
- View in PGS-Catalog
Target study
- Coverage: 33,839 (99.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000759
Reference score
- Variants: 140
- Variants ignored: 0
-
Trait: Hypothyroidism
- Mapped Trait(s):
- Publication: Khan Z et.al, Nat Commun (2021-06-07)
- View in PGS-Catalog
Target study
- Coverage: 137 (97.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000760
Reference score
- Variants: 42
- Variants ignored: 0
-
Trait: Vitiligo
- Mapped Trait(s):
- Samples: 40,258
- Population:
- Publication: Khan Z et.al, Nat Commun (2021-06-07)
- View in PGS-Catalog
Target study
- Coverage: 42 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000761
Reference score
- Variants: 1,099,649
- Variants ignored: 0
-
Trait: Hypothyroidism
- Mapped Trait(s):
- Publication: Khan Z et.al, Nat Commun (2021-06-07)
- View in PGS-Catalog
Target study
- Coverage: 1,096,904 (99.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000762
Reference score
- Variants: 100,325
- Variants ignored: 0
-
Trait: Hearing difficulties
- Mapped Trait(s):
- Samples: 250,389
- Population:
- Publication: Cherny SS et.al, Eur J Hum Genet (2020-03-20)
- View in PGS-Catalog
Target study
- Coverage: 100,163 (99.84%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000763
Reference score
- Variants: 4,270
- Variants ignored: 0
-
Trait: Hearing aid use
- Mapped Trait(s):
- Samples: 253,918
- Population:
- Publication: Cherny SS et.al, Eur J Hum Genet (2020-03-20)
- View in PGS-Catalog
Target study
- Coverage: 4,268 (99.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000764
Reference score
- Variants: 23
- Variants ignored: 10
-
Trait: Primary-open angle glaucoma
- Mapped Trait(s):
- Samples: 0
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Cole BS et.al, Invest Ophthalmol Vis Sci (2021-02-01)
- View in PGS-Catalog
Target study
- Coverage: 13 (56.52%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000765
Reference score
- Variants: 95
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 125,478
- Population:
- European: 95.8%
- East Asian: 4.2%
- Publication: Huyghe JR et.al, Nat Genet (2018-12-03)
- View in PGS-Catalog
Target study
- Coverage: 93 (97.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000766
Reference score
- Variants: 56
- Variants ignored: 27
-
Trait: Cutaneous melanoma
- Mapped Trait(s):
- Samples: 411,948
- Population:
- Publication: Bakshi A et.al, J Natl Cancer Inst (2021-04-10)
- View in PGS-Catalog
Target study
- Coverage: 28 (50%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000767
Reference score
- Variants: 14
- Variants ignored: 2
-
Trait: Depression
- Mapped Trait(s):
- Samples: 650,197
- Population:
- Publication: Guffanti G et.al, Transl Psychiatry (2019-09-19)
- View in PGS-Catalog
Target study
- Coverage: 9 (64.29%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000768
Reference score
- Variants: 68
- Variants ignored: 0
-
Trait: QT-interval
- Mapped Trait(s):
- Samples: 71,061
- Population:
- Publication: Lahrouchi N et.al, Circulation (2020-05-20)
- View in PGS-Catalog
Target study
- Coverage: 68 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000769
Reference score
- Variants: 16
- Variants ignored: 2
-
Trait: Response to bronchodilator (albutamol)
- Mapped Trait(s):
- Samples: 1,644
- Population:
- Publication: Sordillo JE et.al, J Pers Med (2021-04-20)
- View in PGS-Catalog
Target study
- Coverage: 14 (87.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000771
Reference score
- Variants: 95
- Variants ignored: 0
-
Trait: Systemic lupus erythematosus
- Mapped Trait(s):
- Samples: 184,331
- Population:
- European: 53.3%
- East Asian: 32.4%
- Multi-Ancestry (including Europeans): 9.1%
- Multi-Ancestry (excluding Europeans): 2%
- African: 2%
- Hispanic or Latin American: 1.2%
- Publication: Chen L et.al, Hum Mol Genet (2020-06-01)
- View in PGS-Catalog
Target study
- Coverage: 94 (98.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000772
Reference score
- Variants: 95
- Variants ignored: 0
-
Trait: Systemic lupus erythematosus
- Mapped Trait(s):
- Samples: 184,331
- Population:
- European: 53.3%
- East Asian: 32.4%
- Multi-Ancestry (including Europeans): 9.1%
- Multi-Ancestry (excluding Europeans): 2%
- African: 2%
- Hispanic or Latin American: 1.2%
- Publication: Chen L et.al, Hum Mol Genet (2020-06-01)
- View in PGS-Catalog
Target study
- Coverage: 94 (98.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000773
Reference score
- Variants: 179
- Variants ignored: 0
-
Trait: Breast cancer
- Mapped Trait(s):
- Samples: 227,101
- Population:
- Publication: Du Z et.al, J Natl Cancer Inst (2021-03-26)
- View in PGS-Catalog
Target study
- Coverage: 179 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000774
Reference score
- Variants: 179
- Variants ignored: 0
-
Trait: Estrogen receptor positive breast cancer
- Mapped Trait(s):
- Samples: 227,101
- Population:
- Publication: Du Z et.al, J Natl Cancer Inst (2021-03-26)
- View in PGS-Catalog
Target study
- Coverage: 179 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000775
Reference score
- Variants: 179
- Variants ignored: 0
-
Trait: Estrogen receptor negative breast cancer
- Mapped Trait(s):
- Samples: 227,101
- Population:
- Publication: Du Z et.al, J Natl Cancer Inst (2021-03-26)
- View in PGS-Catalog
Target study
- Coverage: 179 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000776
Reference score
- Variants: 9
- Variants ignored: 63
-
Trait: Cirrhosis
- Mapped Trait(s):
- Samples: 168,430
- Population:
- Publication: Innes H et.al, Gastroenterology (2020-06-16)
- View in PGS-Catalog
Target study
- Coverage: 0 (0%) zero
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000777
Reference score
- Variants: 3
- Variants ignored: 0
-
Trait: Parkinsons disease dementia
- Mapped Trait(s):
- Samples: 2,650
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Liu G et.al, Nat Genet (2021-05-06)
- View in PGS-Catalog
Target study
- Coverage: 3 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000778
Reference score
- Variants: 20
- Variants ignored: 0
-
Trait: Hypertrophic cardiomyopathy
- Mapped Trait(s):
- Samples: 8,361
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Tadros R et.al, Nat Genet (2021-01-25)
- View in PGS-Catalog
Target study
- Coverage: 20 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000779
Reference score
- Variants: 7
- Variants ignored: 0
-
Trait: Alzheimer's disease
- Mapped Trait(s):
- Samples: 147,484
- Population:
- European: 91.4%
- Multi-Ancestry (excluding Europeans): 8.6%
- Publication: Zhou X et.al, Alzheimers Dement (Amst) (2020-08-05)
- View in PGS-Catalog
Target study
- Coverage: 7 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000780
Reference score
- Variants: 135
- Variants ignored: 0
-
Trait: Allergic diseases
- Mapped Trait(s):
- Samples: 360,838
- Population:
- Publication: Clark H et.al, Clin Exp Allergy (2019-10-15)
- View in PGS-Catalog
Target study
- Coverage: 135 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000781
Reference score
- Variants: 5
- Variants ignored: 0
-
Trait: Glioma
- Mapped Trait(s):
- Samples: 30,659
- Population:
- Publication: Adel Fahmideh M et.al, Sci Rep (2019-12-02)
- View in PGS-Catalog
Target study
- Coverage: 2 (40%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000782
Reference score
- Variants: 15
- Variants ignored: 0
-
Trait: Bladder cancer
- Mapped Trait(s):
- Samples: 464,396
- Population:
- Publication: Kachuri L et.al, Nat Commun (2020-11-27)
- View in PGS-Catalog
Target study
- Coverage: 14 (93.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000783
Reference score
- Variants: 162
- Variants ignored: 50
-
Trait: Breast cancer
- Mapped Trait(s):
- Samples: 139,274
- Population:
- Publication: Kachuri L et.al, Nat Commun (2020-11-27)
- View in PGS-Catalog
Target study
- Coverage: 153 (94.44%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000784
Reference score
- Variants: 10
- Variants ignored: 9
-
Trait: Cervical cancer
- Mapped Trait(s):
- Samples: 20,405
- Population:
- Publication: Kachuri L et.al, Nat Commun (2020-11-27)
- View in PGS-Catalog
Target study
- Coverage: 9 (90%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000785
Reference score
- Variants: 103
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 403,807
- Population:
- European: 90.3%
- Unknown: 6.5%
- African: 1.6%
- East Asian: 1.3%
- Additional Diverse Ancestries: 0.2%
- Publication: Kachuri L et.al, Nat Commun (2020-11-27)
- View in PGS-Catalog
Target study
- Coverage: 101 (98.06%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000786
Reference score
- Variants: 9
- Variants ignored: 0
-
Trait: Endometrial cancer
- Mapped Trait(s):
- Samples: 43,054
- Population:
- European: 66.4%
- Unknown: 33.6%
- Publication: Kachuri L et.al, Nat Commun (2020-11-27)
- View in PGS-Catalog
Target study
- Coverage: 9 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000787
Reference score
- Variants: 19
- Variants ignored: 0
-
Trait: Kidney cancer
- Mapped Trait(s):
- Samples: 42,061
- Population:
- Publication: Kachuri L et.al, Nat Commun (2020-11-27)
- View in PGS-Catalog
Target study
- Coverage: 16 (84.21%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000788
Reference score
- Variants: 75
- Variants ignored: 0
-
Trait: Lymphocytic leukemiaaa
- Mapped Trait(s):
- Samples: 156,613
- Population:
- European: 78.8%
- Hispanic or Latin American: 8.4%
- Unknown: 6.5%
- African: 3.5%
- Multi-Ancestry (excluding Europeans): 2.8%
- Publication: Kachuri L et.al, Nat Commun (2020-11-27)
- View in PGS-Catalog
Target study
- Coverage: 69 (92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000789
Reference score
- Variants: 109
- Variants ignored: 0
-
Trait: Lung cancer
- Mapped Trait(s):
- Samples: 215,467
- Population:
- Publication: Kachuri L et.al, Nat Commun (2020-11-27)
- View in PGS-Catalog
Target study
- Coverage: 108 (99.08%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000790
Reference score
- Variants: 24
- Variants ignored: 0
-
Trait: Melanoma
- Mapped Trait(s):
- Samples: 365,516
- Population:
- Publication: Kachuri L et.al, Nat Commun (2020-11-27)
- View in PGS-Catalog
Target study
- Coverage: 22 (91.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000791
Reference score
- Variants: 19
- Variants ignored: 9
-
Trait: Non-Hodgkin's lymphoma
- Mapped Trait(s):
- Samples: 34,043
- Population:
- European: 85.3%
- Unknown: 14.7%
- Publication: Kachuri L et.al, Nat Commun (2020-11-27)
- View in PGS-Catalog
Target study
- Coverage: 18 (94.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000792
Reference score
- Variants: 14
- Variants ignored: 9
-
Trait: Oral cavity and pharyngeal cancers
- Mapped Trait(s):
- Samples: 41,845
- Population:
- European: 66%
- Multi-Ancestry (including Europeans): 27.3%
- Unknown: 6.7%
- Publication: Kachuri L et.al, Nat Commun (2020-11-27)
- View in PGS-Catalog
Target study
- Coverage: 10 (71.43%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000793
Reference score
- Variants: 36
- Variants ignored: 0
-
Trait: Ovarian cancer
- Mapped Trait(s):
- Samples: 152,183
- Population:
- Publication: Kachuri L et.al, Nat Commun (2020-11-27)
- View in PGS-Catalog
Target study
- Coverage: 35 (97.22%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000794
Reference score
- Variants: 22
- Variants ignored: 0
-
Trait: Pancreatic cancer
- Mapped Trait(s):
- Samples: 57,275
- Population:
- European: 86.6%
- Unknown: 12.3%
- Multi-Ancestry (excluding Europeans): 1.1%
- Publication: Kachuri L et.al, Nat Commun (2020-11-27)
- View in PGS-Catalog
Target study
- Coverage: 22 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000795
Reference score
- Variants: 161
- Variants ignored: 46
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 461,661
- Population:
- European: 93.4%
- African: 2.8%
- East Asian: 2.5%
- Hispanic or Latin American: 1.2%
- Unknown: 0.1%
- Publication: Kachuri L et.al, Nat Commun (2020-11-27)
- View in PGS-Catalog
Target study
- Coverage: 152 (94.41%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000796
Reference score
- Variants: 52
- Variants ignored: 0
-
Trait: Testicular cancer
- Mapped Trait(s):
- Samples: 56,799
- Population:
- Publication: Kachuri L et.al, Nat Commun (2020-11-27)
- View in PGS-Catalog
Target study
- Coverage: 50 (96.15%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000797
Reference score
- Variants: 12
- Variants ignored: 8
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Samples: 291,738
- Population:
- Publication: Kachuri L et.al, Nat Commun (2020-11-27)
- View in PGS-Catalog
Target study
- Coverage: 11 (91.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000798
Reference score
- Variants: 157
- Variants ignored: 0
-
Trait: Coronary heart disease
- Mapped Trait(s):
- Samples: 547,261
- Population:
- Publication: Severance LM et.al, J Cardiovasc Comput Tomogr (2019-05-09)
- View in PGS-Catalog
Target study
- Coverage: 157 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000799
Reference score
- Variants: 22
- Variants ignored: 8
-
Trait: Asthma
- Mapped Trait(s):
- Samples: 169,861
- Population:
- European: 87.4%
- East Asian: 6.1%
- Multi-Ancestry (excluding Europeans): 4.8%
- Hispanic or Latin American: 1.6%
- Publication: Dijk FN et.al, J Allergy Clin Immunol (2019-05-27)
- View in PGS-Catalog
Target study
- Coverage: 14 (63.64%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000800
Reference score
- Variants: 133
- Variants ignored: 29
-
Trait: Allergic disease
- Mapped Trait(s):
- Samples: 360,838
- Population:
- Publication: Dijk FN et.al, J Allergy Clin Immunol (2019-05-27)
- View in PGS-Catalog
Target study
- Coverage: 104 (78.2%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000801
Reference score
- Variants: 40
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 220,743
- Population:
- European: 77.2%
- East Asian: 19.8%
- African: 3%
- Publication: Hang D et.al, Int J Epidemiol (2020-02-01)
- View in PGS-Catalog
Target study
- Coverage: 40 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000802
Reference score
- Variants: 19
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 111,769
- Population:
- European: 63.6%
- East Asian: 36.4%
- Publication: He CY et.al, Genomics (2021-02-02)
- View in PGS-Catalog
Target study
- Coverage: 0 (0%) zero
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000803
Reference score
- Variants: 41
- Variants ignored: 0
-
Trait: Systemic lupus erythematosus
- Mapped Trait(s):
- Samples: 14,267
- Population:
- Publication: Kawai VK et.al, Lupus (2021-05-12)
- View in PGS-Catalog
Target study
- Coverage: 41 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000804
Reference score
- Variants: 582
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 2,814,564
- Population:
- European: 79.2%
- Multi-Ancestry (excluding Europeans): 15.4%
- African: 4%
- Hispanic or Latin American: 1.5%
- Publication: Polfus LM et.al, HGG Adv (2021-03-09)
- View in PGS-Catalog
Target study
- Coverage: 582 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000805
Reference score
- Variants: 582
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 1,114,458
- Population:
- Publication: Polfus LM et.al, HGG Adv (2021-03-09)
- View in PGS-Catalog
Target study
- Coverage: 582 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000806
Reference score
- Variants: 582
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 56,092
- Population:
- Publication: Polfus LM et.al, HGG Adv (2021-03-09)
- View in PGS-Catalog
Target study
- Coverage: 582 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000807
Reference score
- Variants: 582
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 216,287
- Population:
- Multi-Ancestry (excluding Europeans): 100%
- Publication: Polfus LM et.al, HGG Adv (2021-03-09)
- View in PGS-Catalog
Target study
- Coverage: 582 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000808
Reference score
- Variants: 582
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 20,445
- Population:
- Hispanic or Latin American: 100%
- Publication: Polfus LM et.al, HGG Adv (2021-03-09)
- View in PGS-Catalog
Target study
- Coverage: 582 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000809
Reference score
- Variants: 127
- Variants ignored: 33
-
Trait: Multiple sclerosis
- Mapped Trait(s):
- Samples: 75,982
- Population:
- Publication: Barnes CLK et.al, Eur J Hum Genet (2021-06-04)
- View in PGS-Catalog
Target study
- Coverage: 73 (57.48%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000810
Reference score
- Variants: 136
- Variants ignored: 0
-
Trait: Allergic disease (asthma, hay fever or eczema)
- Mapped Trait(s):
- Samples: 360,838
- Population:
- Publication: Ferreira MA et.al, Nat Genet (2017-10-30)
- View in PGS-Catalog
Target study
- Coverage: 136 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000811
Reference score
- Variants: 39
- Variants ignored: 21
-
Trait: Alzheimer's disease
- Mapped Trait(s):
- Samples: 644,112
- Population:
- Publication: Najar J et.al, Alzheimers Dement (Amst) (2021-01-22)
- View in PGS-Catalog
Target study
- Coverage: 17 (43.59%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000812
Reference score
- Variants: 57
- Variants ignored: 15
-
Trait: Alzheimer's disease
- Mapped Trait(s):
- Samples: 63,926
- Population:
- Publication: Najar J et.al, Alzheimers Dement (Amst) (2021-01-22)
- View in PGS-Catalog
Target study
- Coverage: 42 (73.68%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000813
Reference score
- Variants: 46
- Variants ignored: 0
-
Trait: melanoma
- Mapped Trait(s):
- Samples: 36,077
- Population:
- Publication: Potjer TP et.al, J Med Genet (2020-09-29)
- View in PGS-Catalog
Target study
- Coverage: 45 (97.83%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000815
Reference score
- Variants: 290
- Variants ignored: 0
-
Trait: Alkaline phosphatase
- Mapped Trait(s):
- Samples: 437,438
- Population:
- Publication: Pazoki R et.al, Nat Commun (2021-05-10)
- View in PGS-Catalog
Target study
- Coverage: 287 (98.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000816
Reference score
- Variants: 150
- Variants ignored: 0
-
Trait: Alanine transaminase
- Mapped Trait(s):
- EFO_0004735: serum alanine aminotransferase measurement
- Samples: 437,267
- Population:
- Publication: Pazoki R et.al, Nat Commun (2021-05-10)
- View in PGS-Catalog
Target study
- Coverage: 148 (98.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000817
Reference score
- Variants: 200
- Variants ignored: 0
-
Trait: Gamma-glutamyl transferase
- Mapped Trait(s):
- EFO_0004532: serum gamma-glutamyl transferase measurement
- Samples: 437,194
- Population:
- Publication: Pazoki R et.al, Nat Commun (2021-05-10)
- View in PGS-Catalog
Target study
- Coverage: 200 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000818
Reference score
- Variants: 138
- Variants ignored: 0
-
Trait: Coronary heart disease
- Mapped Trait(s):
- Samples: 1,022,858
- Population:
- Unknown: 78%
- Multi-Ancestry (including Europeans): 19%
- European: 3%
- Publication: Bauer A et.al, Genet Epidemiol (2021-06-03)
- View in PGS-Catalog
Target study
- Coverage: 138 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000819
Reference score
- Variants: 3,537,914
- Variants ignored: 0
-
Trait: Diabetic retinopathy
- Mapped Trait(s):
- Samples: 17,567
- Population:
- Publication: Forrest IS et.al, Hum Mol Genet (2021-05-01)
- View in PGS-Catalog
Target study
- Coverage: 3,537,914 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000820
Reference score
- Variants: 890,908
- Variants ignored: 0
-
Trait: Hypothyroidism (self-reported)
- Mapped Trait(s):
- Samples: 459,318
- Population:
- Publication: Luo J et.al, Clin Cancer Res (2021-07-08)
- View in PGS-Catalog
Target study
- Coverage: 890,908 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000821
Reference score
- Variants: 872,391
- Variants ignored: 0
-
Trait: Thyroid medication use
- Mapped Trait(s):
- Samples: 305,582
- Population:
- Publication: Luo J et.al, Clin Cancer Res (2021-07-08)
- View in PGS-Catalog
Target study
- Coverage: 872,391 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000822
Reference score
- Variants: 59
- Variants ignored: 0
-
Trait: Urinary albumin to creatinine ratio
- Mapped Trait(s):
- Samples: 564,257
- Population:
- European: 97%
- African: 1.2%
- East Asian: 1.1%
- South Asian: 0.4%
- Hispanic or Latin American: 0.3%
- Publication: Teumer A et.al, Nat Commun (2019-09-11)
- View in PGS-Catalog
Target study
- Coverage: 58 (98.31%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000823
Reference score
- Variants: 23
- Variants ignored: 0
-
Trait: Alzheimer's disease
- Mapped Trait(s):
- Samples: 361,206
- Population:
- Multi-Ancestry (including Europeans): 56.6%
- European: 34%
- Unknown: 9.5%
- Publication: van der Lee SJ et.al, Lancet Neurol (2018-03-16)
- View in PGS-Catalog
Target study
- Coverage: 21 (91.3%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000824
Reference score
- Variants: 809
- Variants ignored: 0
-
Trait: Low-density lipoprotein cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 94,595
- Population:
- Publication: Zubair N et.al, Sci Rep (2019-05-02)
- View in PGS-Catalog
Target study
- Coverage: 800 (98.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000825
Reference score
- Variants: 883
- Variants ignored: 0
-
Trait: High-density lipoprotein cholesterol
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 94,595
- Population:
- Publication: Zubair N et.al, Sci Rep (2019-05-02)
- View in PGS-Catalog
Target study
- Coverage: 876 (99.21%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000826
Reference score
- Variants: 769
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 94,595
- Population:
- Publication: Zubair N et.al, Sci Rep (2019-05-02)
- View in PGS-Catalog
Target study
- Coverage: 753 (97.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000827
Reference score
- Variants: 113
- Variants ignored: 0
-
Trait: Waist circumference (male)
- Mapped Trait(s):
- Samples: 142,762
- Population:
- Publication: Zubair N et.al, Sci Rep (2019-05-02)
- View in PGS-Catalog
Target study
- Coverage: 113 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000828
Reference score
- Variants: 149
- Variants ignored: 0
-
Trait: Waist circumference (female)
- Mapped Trait(s):
- Samples: 142,762
- Population:
- Publication: Zubair N et.al, Sci Rep (2019-05-02)
- View in PGS-Catalog
Target study
- Coverage: 149 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000829
Reference score
- Variants: 290
- Variants ignored: 0
-
Trait: Body mass index (male)
- Mapped Trait(s):
- Samples: 238,944
- Population:
- European: 99.1%
- Hispanic or Latin American: 0.5%
- African: 0.4%
- Publication: Zubair N et.al, Sci Rep (2019-05-02)
- View in PGS-Catalog
Target study
- Coverage: 287 (98.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000830
Reference score
- Variants: 372
- Variants ignored: 0
-
Trait: Body mass index (female)
- Mapped Trait(s):
- Samples: 238,944
- Population:
- European: 99.1%
- Hispanic or Latin American: 0.5%
- African: 0.4%
- Publication: Zubair N et.al, Sci Rep (2019-05-02)
- View in PGS-Catalog
Target study
- Coverage: 369 (99.19%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000831
Reference score
- Variants: 1,032
- Variants ignored: 0
-
Trait: Total cholesterol
- Mapped Trait(s):
- Samples: 283,785
- Population:
- Publication: Zubair N et.al, Sci Rep (2019-05-02)
- View in PGS-Catalog
Target study
- Coverage: 1,017 (98.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000832
Reference score
- Variants: 384
- Variants ignored: 72
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 574,306
- Population:
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 309 (80.47%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000834
Reference score
- Variants: 220
- Variants ignored: 49
-
Trait: Corrected insulin response (at 30mins during OGTT)
- Mapped Trait(s):
- Samples: 4,789
- Population:
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 171 (77.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000835
Reference score
- Variants: 319
- Variants ignored: 65
-
Trait: Insulin secretion rate
- Mapped Trait(s):
- Samples: 4,828
- Population:
- Hispanic or Latin American: 48.4%
- European: 44.7%
- Additional Diverse Ancestries: 6.9%
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 254 (79.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000836
Reference score
- Variants: 223
- Variants ignored: 51
-
Trait: Fasting Insulin
- Mapped Trait(s):
- Samples: 51,750
- Population:
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 172 (77.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000837
Reference score
- Variants: 219
- Variants ignored: 52
-
Trait: Insulin sensitivity index
- Mapped Trait(s):
- Samples: 16,753
- Population:
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 167 (76.26%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000838
Reference score
- Variants: 224
- Variants ignored: 54
-
Trait: Fasting Glucose
- Mapped Trait(s):
- Samples: 51,750
- Population:
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 170 (75.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000839
Reference score
- Variants: 219
- Variants ignored: 54
-
Trait: Two hour glucose during OGTT
- Mapped Trait(s):
- Samples: 15,234
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 165 (75.34%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000840
Reference score
- Variants: 223
- Variants ignored: 54
-
Trait: Fasting Proinsulin
- Mapped Trait(s):
- Samples: 10,701
- Population:
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 169 (75.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000841
Reference score
- Variants: 122
- Variants ignored: 25
-
Trait: Body mass index
- Mapped Trait(s):
- Samples: 238,944
- Population:
- European: 99.1%
- Hispanic or Latin American: 0.5%
- African: 0.4%
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 97 (79.51%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000842
Reference score
- Variants: 39
- Variants ignored: 7
-
Trait: Waist-hip ratio
- Mapped Trait(s):
- Samples: 142,762
- Population:
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 32 (82.05%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000843
Reference score
- Variants: 63
- Variants ignored: 12
-
Trait: WHR adjusted for BMI
- Mapped Trait(s):
- Samples: 142,762
- Population:
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 51 (80.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000844
Reference score
- Variants: 518
- Variants ignored: 100
-
Trait: Predicted visceral adipose tissue
- Mapped Trait(s):
- Samples: 325,153
- Population:
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 417 (80.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000845
Reference score
- Variants: 303
- Variants ignored: 64
-
Trait: High density lipoprotein (HDL)
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 94,595
- Population:
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 236 (77.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000846
Reference score
- Variants: 275
- Variants ignored: 45
-
Trait: Low density lipoprotein (LDL)
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 94,595
- Population:
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 229 (83.27%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000847
Reference score
- Variants: 201
- Variants ignored: 42
-
Trait: Triglycerides (TG)
- Mapped Trait(s):
- Samples: 94,595
- Population:
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 158 (78.61%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000848
Reference score
- Variants: 6
- Variants ignored: 1
-
Trait: Type 2 diabetes (based on SNPs associated with adiposity)
- Mapped Trait(s):
- Samples: 298,957
- Population:
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 5 (83.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000849
Reference score
- Variants: 3
- Variants ignored: 0
-
Trait: Type 2 diabetes (based on SNPs associated with impaired lipids)
- Mapped Trait(s):
- Samples: 298,957
- Population:
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 3 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000850
Reference score
- Variants: 16
- Variants ignored: 2
-
Trait: Type 2 diabetes (based on SNPs associated with insulin action)
- Mapped Trait(s):
- Samples: 298,957
- Population:
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 14 (87.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000851
Reference score
- Variants: 37
- Variants ignored: 8
-
Trait: Type 2 diabetes (based on SNPs associated with insulin action/secretion)
- Mapped Trait(s):
- Samples: 298,957
- Population:
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 28 (75.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000852
Reference score
- Variants: 8
- Variants ignored: 1
-
Trait: Type 2 diabetes (based on SNPs associated with insulin secretion)
- Mapped Trait(s):
- Samples: 298,957
- Population:
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 7 (87.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000853
Reference score
- Variants: 21
- Variants ignored: 6
-
Trait: Type 2 diabetes (based on SNPs associated with insulin secretion)
- Mapped Trait(s):
- Samples: 298,957
- Population:
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 15 (71.43%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000854
Reference score
- Variants: 27
- Variants ignored: 7
-
Trait: Type 2 diabetes (based on SNPs associated with beta cell function)
- Mapped Trait(s):
- Samples: 17,365
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 20 (74.07%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000855
Reference score
- Variants: 18
- Variants ignored: 2
-
Trait: Type 2 diabetes (based on SNPs associated with lipodystrophy)
- Mapped Trait(s):
- Samples: 17,365
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 16 (88.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000856
Reference score
- Variants: 3
- Variants ignored: 0
-
Trait: Type 2 diabetes (based on SNPs associated with liver lipids)
- Mapped Trait(s):
- Samples: 17,365
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 3 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000857
Reference score
- Variants: 4
- Variants ignored: 0
-
Trait: Type 2 diabetes (based on SNPs associated with obesity)
- Mapped Trait(s):
- Samples: 17,365
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 4 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000858
Reference score
- Variants: 6
- Variants ignored: 1
-
Trait: Type 2 diabetes (based on SNPs associated with proinsulin levels)
- Mapped Trait(s):
- Samples: 17,365
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 5 (83.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000859
Reference score
- Variants: 34
- Variants ignored: 2
-
Trait: Chronic kidney disease
- Mapped Trait(s):
- Samples: 625,219
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 32 (94.12%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000860
Reference score
- Variants: 625
- Variants ignored: 129
-
Trait: Estimated glomerular filtration rate
- Mapped Trait(s):
- Samples: 625,219
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 496 (79.36%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000861
Reference score
- Variants: 93
- Variants ignored: 20
-
Trait: Urine Albumin-to-Creatinine ratio
- Mapped Trait(s):
- Samples: 564,257
- Population:
- European: 97%
- African: 1.2%
- East Asian: 1.1%
- South Asian: 0.4%
- Hispanic or Latin American: 0.3%
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 73 (78.49%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000862
Reference score
- Variants: 30
- Variants ignored: 5
-
Trait: Diabetic Retinopathy
- Mapped Trait(s):
- Samples: 4,323
- Population:
- European: 60.5%
- African: 39.5%
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 14 (46.67%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000863
Reference score
- Variants: 330
- Variants ignored: 67
-
Trait: Cardiovascular disease
- Mapped Trait(s):
- Samples: 250,736
- Population:
- Publication: Aly DM et.al, Nat Genet (2021-11-04)
- View in PGS-Catalog
Target study
- Coverage: 260 (78.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000865
Reference score
- Variants: 4
- Variants ignored: 0
-
Trait: Hepatic fat content
- Mapped Trait(s):
- Samples: 17,458
- Population:
- European: 65.2%
- African: 19.9%
- East Asian: 7.6%
- Hispanic or Latin American: 6.5%
- Unknown: 0.8%
- Publication: Dongiovanni P et.al, J Intern Med (2017-12-27)
- View in PGS-Catalog
Target study
- Coverage: 3 (75%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000866
Reference score
- Variants: 4
- Variants ignored: 0
-
Trait: Hepatic fat content
- Mapped Trait(s):
- Samples: 17,458
- Population:
- European: 65.2%
- African: 19.9%
- East Asian: 7.6%
- Hispanic or Latin American: 6.5%
- Unknown: 0.8%
- Publication: Dongiovanni P et.al, J Intern Med (2017-12-27)
- View in PGS-Catalog
Target study
- Coverage: 3 (75%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000867
Reference score
- Variants: 10
- Variants ignored: 0
-
Trait: Allergy
- Mapped Trait(s):
- Samples: 53,862
- Population:
- Publication: Arabkhazaeli A et.al, Pediatr Allergy Immunol (2017-11-22)
- View in PGS-Catalog
Target study
- Coverage: 3 (30%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000868
Reference score
- Variants: 221
- Variants ignored: 0
-
Trait: Type II diabetes
- Mapped Trait(s):
- Samples: 898,130
- Population:
- Publication: Aksit MA et.al, J Clin Endocrinol Metab (2020-05-01)
- View in PGS-Catalog
Target study
- Coverage: 221 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000869
Reference score
- Variants: 48
- Variants ignored: 0
-
Trait: Type I diabetes
- Mapped Trait(s):
- Samples: 29,652
- Population:
- Publication: Aksit MA et.al, J Clin Endocrinol Metab (2020-05-01)
- View in PGS-Catalog
Target study
- Coverage: 48 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000870
Reference score
- Variants: 18
- Variants ignored: 0
-
Trait: Cystic fibrosis related diabetes
- Mapped Trait(s):
- Samples: 5,740
- Population:
- Publication: Aksit MA et.al, J Clin Endocrinol Metab (2020-05-01)
- View in PGS-Catalog
Target study
- Coverage: 18 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000871
Reference score
- Variants: 14
- Variants ignored: 0
-
Trait: Insulin secretion
- Mapped Trait(s):
- Samples: 159,208
- Population:
- Publication: Aksit MA et.al, J Clin Endocrinol Metab (2020-05-01)
- View in PGS-Catalog
Target study
- Coverage: 14 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000872
Reference score
- Variants: 5
- Variants ignored: 0
-
Trait: Non-alcoholic fatty liver disease
- Mapped Trait(s):
- Samples: 64,002
- Population:
- European: 90.5%
- African: 5.4%
- East Asian: 2.1%
- Hispanic or Latin American: 1.8%
- Unknown: 0.2%
- Publication: Bianco C et.al, J Hepatol (2020-11-25)
- View in PGS-Catalog
Target study
- Coverage: 4 (80%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000874
Reference score
- Variants: 41
- Variants ignored: 8
-
Trait: Chronic lymphocytic leukemia
- Mapped Trait(s):
- Samples: 17,691
- Population:
- Publication: Kleinstern G et.al, Blood (2018-04-19)
- View in PGS-Catalog
Target study
- Coverage: 33 (80.49%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000875
Reference score
- Variants: 36
- Variants ignored: 0
-
Trait: Low-density lipoprotein cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 94,595
- Population:
- Publication: Leal LG et.al, Mol Genet Genomic Med (2020-04-19)
- View in PGS-Catalog
Target study
- Coverage: 35 (97.22%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000876
Reference score
- Variants: 31
- Variants ignored: 5
-
Trait: Alzheimer's disease
- Mapped Trait(s):
- Samples: 43,708
- Population:
- Publication: Leonenko G et.al, Ann Clin Transl Neurol (2019-02-18)
- View in PGS-Catalog
Target study
- Coverage: 25 (80.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000877
Reference score
- Variants: 53
- Variants ignored: 0
-
Trait: Insulin resistance
- Mapped Trait(s):
- Samples: 349,497
- Population:
- Publication: Lotta LA et.al, Nat Genet (2016-11-14)
- View in PGS-Catalog
Target study
- Coverage: 53 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000878
Reference score
- Variants: 4
- Variants ignored: 1
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 3,178
- Population:
- Publication: Oh JJ et.al, Front Oncol (2020-10-22)
- View in PGS-Catalog
Target study
- Coverage: 1 (25%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000879
Reference score
- Variants: 146
- Variants ignored: 0
-
Trait: Intraocular pressure
- Mapped Trait(s):
- Samples: 133,492
- Population:
- Publication: Qassim A et.al, Ophthalmology (2020-01-07)
- View in PGS-Catalog
Target study
- Coverage: 146 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000880
Reference score
- Variants: 18
- Variants ignored: 0
-
Trait: Lung cancer
- Mapped Trait(s):
- Samples: 85,716
- Population:
- Publication: Xie J et.al, Sleep (2021-04-05)
- View in PGS-Catalog
Target study
- Coverage: 17 (94.44%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000881
Reference score
- Variants: 72
- Variants ignored: 15
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 374,196
- Population:
- European: 92.4%
- African: 3.4%
- East Asian: 2.7%
- Hispanic or Latin American: 1.5%
- Publication: Xu J et.al, Prostate (2021-05-06)
- View in PGS-Catalog
Target study
- Coverage: 52 (72.22%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000882
Reference score
- Variants: 1,094,650
- Variants ignored: 0
-
Trait: 25-hydroxyvitamin D
- Mapped Trait(s):
- Samples: 417,580
- Population:
- Publication: Revez JA et.al, Nat Commun (2020-04-02)
- View in PGS-Catalog
Target study
- Coverage: 1,092,014 (99.76%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000883
Reference score
- Variants: 1,477,661
- Variants ignored: 0
-
Trait: Estimated glomerular filtration rate
- Mapped Trait(s):
- Samples: 1,159,871
- Population:
- European: 81.8%
- East Asian: 14.4%
- South Asian: 1.8%
- African: 1.5%
- Hispanic or Latin American: 0.4%
- Publication: Yu Z et.al, J Am Soc Nephrol (2021-09-21)
- View in PGS-Catalog
Target study
- Coverage: 1,477,661 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000884
Reference score
- Variants: 40,042
- Variants ignored: 0
-
Trait: Estimated glomerular filtration rate
- Mapped Trait(s):
- Samples: 1,159,871
- Population:
- European: 81.8%
- East Asian: 14.4%
- South Asian: 1.8%
- African: 1.5%
- Hispanic or Latin American: 0.4%
- Publication: Yu Z et.al, J Am Soc Nephrol (2021-09-21)
- View in PGS-Catalog
Target study
- Coverage: 40,042 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000885
Reference score
- Variants: 1,460
- Variants ignored: 0
-
Trait: Estimated glomerular filtration rate
- Mapped Trait(s):
- Samples: 1,159,871
- Population:
- European: 81.8%
- East Asian: 14.4%
- South Asian: 1.8%
- African: 1.5%
- Hispanic or Latin American: 0.4%
- Publication: Yu Z et.al, J Am Soc Nephrol (2021-09-21)
- View in PGS-Catalog
Target study
- Coverage: 1,460 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000886
Reference score
- Variants: 1,222,318
- Variants ignored: 0
-
Trait: Low density lipoprotein (LDL) cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 87,760
- Population:
- Publication: Graham SE et.al, Nature (2021-12-09)
- View in PGS-Catalog
Target study
- Coverage: 1,222,318 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000887
Reference score
- Variants: 295
- Variants ignored: 0
-
Trait: Low density lipoprotein (LDL) cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 87,760
- Population:
- Publication: Graham SE et.al, Nature (2021-12-09)
- View in PGS-Catalog
Target study
- Coverage: 295 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000888
Reference score
- Variants: 1,239,184
- Variants ignored: 0
-
Trait: Low density lipoprotein (LDL) cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 1,088,526
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Graham SE et.al, Nature (2021-12-09)
- View in PGS-Catalog
Target study
- Coverage: 1,238,649 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000889
Reference score
- Variants: 9,009
- Variants ignored: 0
-
Trait: Low density lipoprotein (LDL) cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 1,088,526
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Graham SE et.al, Nature (2021-12-09)
- View in PGS-Catalog
Target study
- Coverage: 8,983 (99.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000890
Reference score
- Variants: 1,029,158
- Variants ignored: 0
-
Trait: Low density lipoprotein (LDL) cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 82,587
- Population:
- Publication: Graham SE et.al, Nature (2021-12-09)
- View in PGS-Catalog
Target study
- Coverage: 1,029,158 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000891
Reference score
- Variants: 66
- Variants ignored: 0
-
Trait: Low density lipoprotein (LDL) cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 82,587
- Population:
- Publication: Graham SE et.al, Nature (2021-12-09)
- View in PGS-Catalog
Target study
- Coverage: 66 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000892
Reference score
- Variants: 1,119,211
- Variants ignored: 0
-
Trait: Low density lipoprotein (LDL) cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 831,666
- Population:
- Publication: Graham SE et.al, Nature (2021-12-09)
- View in PGS-Catalog
Target study
- Coverage: 1,119,211 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000893
Reference score
- Variants: 5,427
- Variants ignored: 0
-
Trait: Low density lipoprotein (LDL) cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 831,666
- Population:
- Publication: Graham SE et.al, Nature (2021-12-09)
- View in PGS-Catalog
Target study
- Coverage: 5,403 (99.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000894
Reference score
- Variants: 1,175,595
- Variants ignored: 0
-
Trait: Low density lipoprotein (LDL) cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 46,040
- Population:
- Hispanic or Latin American: 100%
- Publication: Graham SE et.al, Nature (2021-12-09)
- View in PGS-Catalog
Target study
- Coverage: 1,175,263 (99.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000895
Reference score
- Variants: 76
- Variants ignored: 0
-
Trait: Low density lipoprotein (LDL) cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 46,040
- Population:
- Hispanic or Latin American: 100%
- Publication: Graham SE et.al, Nature (2021-12-09)
- View in PGS-Catalog
Target study
- Coverage: 76 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000896
Reference score
- Variants: 1,100,062
- Variants ignored: 0
-
Trait: Low density lipoprotein (LDL) cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 33,658
- Population:
- Publication: Graham SE et.al, Nature (2021-12-09)
- View in PGS-Catalog
Target study
- Coverage: 1,099,858 (99.98%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000897
Reference score
- Variants: 13
- Variants ignored: 0
-
Trait: Low density lipoprotein (LDL) cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 33,658
- Population:
- Publication: Graham SE et.al, Nature (2021-12-09)
- View in PGS-Catalog
Target study
- Coverage: 13 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000898
Reference score
- Variants: 40
- Variants ignored: 0
-
Trait: Alzheimer's disease
- Mapped Trait(s):
- Samples: 409,435
- Population:
- Publication: de Rojas I et.al, Nat Commun (2021-06-07)
- View in PGS-Catalog
Target study
- Coverage: 38 (95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000899
Reference score
- Variants: 176
- Variants ignored: 7
-
Trait: Coronary heart disease
- Mapped Trait(s):
- Samples: 1,716,874
- Population:
- Unknown: 63.8%
- European: 17%
- Multi-Ancestry (including Europeans): 15%
- South Asian: 1.9%
- East Asian: 1.3%
- African: 0.6%
- Hispanic or Latin American: 0.2%
- Greater Middle Eastern: 0.1%
- Publication: Feitosa MF et.al, Circ Genom Precis Med (2021-04-12)
- View in PGS-Catalog
Target study
- Coverage: 169 (96.02%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000900
Reference score
- Variants: 1,097,704
- Variants ignored: 0
-
Trait: Systolic blood pressure (female)
- Mapped Trait(s):
- Samples: 194,174
- Population:
- Publication: Kauko A et.al, Hypertension (2021-08-15)
- View in PGS-Catalog
Target study
- Coverage: 1,097,703 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000901
Reference score
- Variants: 1,097,704
- Variants ignored: 0
-
Trait: Systolic blood pressure (male)
- Mapped Trait(s):
- Samples: 167,020
- Population:
- Publication: Kauko A et.al, Hypertension (2021-08-15)
- View in PGS-Catalog
Target study
- Coverage: 1,097,703 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000902
Reference score
- Variants: 90
- Variants ignored: 18
-
Trait: Parkinson's disease
- Mapped Trait(s):
- Samples: 1,474,097
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Nalls MA et.al, Lancet Neurol (2019-12-01)
- View in PGS-Catalog
Target study
- Coverage: 70 (77.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000903
Reference score
- Variants: 1,805
- Variants ignored: 290
-
Trait: Parkinson's disease
- Mapped Trait(s):
- Samples: 1,474,097
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Nalls MA et.al, Lancet Neurol (2019-12-01)
- View in PGS-Catalog
Target study
- Coverage: 1,502 (83.21%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000906
Reference score
- Variants: 330
- Variants ignored: 0
-
Trait: Longevity
- Mapped Trait(s):
- Samples: 500,193
- Population:
- Publication: Tesi N et.al, J Gerontol A Biol Sci Med Sci (2021-04-01)
- View in PGS-Catalog
Target study
- Coverage: 330 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000907
Reference score
- Variants: 1,773,528
- Variants ignored: 0
-
Trait: Major depressive disorder
- Mapped Trait(s):
- Samples: 322,580
- Population:
- Publication: Campos AI et.al, medRxiv (2021-07-16)
- View in PGS-Catalog
Target study
- Coverage: 1,773,528 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000908
Reference score
- Variants: 2,746,982
- Variants ignored: 0
-
Trait: Insomnia
- Mapped Trait(s):
- Samples: 1,331,010
- Population:
- Publication: Campos AI et.al, medRxiv (2021-07-16)
- View in PGS-Catalog
Target study
- Coverage: 2,746,982 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000909
Reference score
- Variants: 2,862,172
- Variants ignored: 0
-
Trait: Headache
- Mapped Trait(s):
- Samples: 441,088
- Population:
- Publication: Campos AI et.al, medRxiv (2021-07-16)
- View in PGS-Catalog
Target study
- Coverage: 2,862,172 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000910
Reference score
- Variants: 735,440
- Variants ignored: 0
-
Trait: Body mass index
- Mapped Trait(s):
- Samples: 681,275
- Population:
- European: 67%
- Unknown: 33%
- Publication: Campos AI et.al, medRxiv (2021-07-16)
- View in PGS-Catalog
Target study
- Coverage: 735,440 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000911
Reference score
- Variants: 530,933
- Variants ignored: 0
-
Trait: Ischemic stroke
- Mapped Trait(s):
- Samples: 446,696
- Population:
- Publication: O'Sullivan JW et.al, Circ Genom Precis Med (2021-06-15)
- View in PGS-Catalog
Target study
- Coverage: 529,505 (99.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000912
Reference score
- Variants: 1,097,704
- Variants ignored: 0
-
Trait: Diastolic blood pressure
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Vaura F et.al, Hypertension (2021-02-22)
- View in PGS-Catalog
Target study
- Coverage: 1,097,703 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000913
Reference score
- Variants: 1,097,704
- Variants ignored: 0
-
Trait: Systolic blood pressure
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Vaura F et.al, Hypertension (2021-02-22)
- View in PGS-Catalog
Target study
- Coverage: 1,097,703 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000914
Reference score
- Variants: 6
- Variants ignored: 0
-
Trait: Abnormal electrocardiogram
- Mapped Trait(s):
- Samples: 1,006
- Population:
- Publication: Wang M et.al, Sci Rep (2021-02-25)
- View in PGS-Catalog
Target study
- Coverage: 5 (83.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000921
Reference score
- Variants: 1,947,711
- Variants ignored: 0
-
Trait: Body mass index
- Mapped Trait(s):
- Samples: 681,275
- Population:
- European: 67%
- Unknown: 33%
- Publication: Borisevich D et.al, PLoS One (2021-10-18)
- View in PGS-Catalog
Target study
- Coverage: 1,943,008 (99.76%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000922
Reference score
- Variants: 12
- Variants ignored: 18
-
Trait: Sarcoidosis
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 10 (83.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000923
Reference score
- Variants: 22
- Variants ignored: 18
-
Trait: Sarcoidosis (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 16 (72.73%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000924
Reference score
- Variants: 5
- Variants ignored: 0
-
Trait: Disorders of porphyrin and bilirubin metabolism (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 5 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000925
Reference score
- Variants: 402
- Variants ignored: 18
-
Trait: Unspecified acute lower respiratory infection (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 353 (87.81%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000926
Reference score
- Variants: 4,194
- Variants ignored: 0
-
Trait: Daytime dozing / sleeping (narcolepsy)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3,927 (93.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000927
Reference score
- Variants: 242
- Variants ignored: 18
-
Trait: Other dermatitis (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 225 (92.98%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000928
Reference score
- Variants: 170
- Variants ignored: 0
-
Trait: Other non-toxic goitre (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 162 (95.29%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000929
Reference score
- Variants: 6
- Variants ignored: 0
-
Trait: All cause dementia (algorithmically-defined)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 5 (83.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000930
Reference score
- Variants: 118
- Variants ignored: 0
-
Trait: Blood clot (diagnosed by doctor)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 101 (85.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000931
Reference score
- Variants: 534
- Variants ignored: 0
-
Trait: Blood clot or deep vein thrombosis (diagnosed by doctor)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 471 (88.2%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000932
Reference score
- Variants: 111
- Variants ignored: 0
-
Trait: Other intervertebral disk disorders (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 98 (88.29%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000933
Reference score
- Variants: 433
- Variants ignored: 18
-
Trait: Nasal polyp (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 367 (84.76%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000934
Reference score
- Variants: 129
- Variants ignored: 9
-
Trait: Nasal polyps
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 107 (82.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000935
Reference score
- Variants: 370
- Variants ignored: 0
-
Trait: High blood pressure, age at diagnosis
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 346 (93.51%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000936
Reference score
- Variants: 5,987
- Variants ignored: 18
-
Trait: High cholesterol
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 5,567 (92.98%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000937
Reference score
- Variants: 2,603
- Variants ignored: 0
-
Trait: Varicose veins
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,437 (93.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000938
Reference score
- Variants: 2,563
- Variants ignored: 18
-
Trait: Varicose veins of lower extremities (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,381 (92.9%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000939
Reference score
- Variants: 2,553
- Variants ignored: 0
-
Trait: Hiatus hernia
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,338 (91.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000940
Reference score
- Variants: 443
- Variants ignored: 36
-
Trait: Intestinal malabsorption (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 399 (90.07%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000941
Reference score
- Variants: 1
- Variants ignored: 9
-
Trait: Iridocyclitis (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 0 (0%) zero
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000942
Reference score
- Variants: 391
- Variants ignored: 0
-
Trait: Cholecystitis
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 354 (90.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000943
Reference score
- Variants: 5
- Variants ignored: 0
-
Trait: Cholecystitis (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 5 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000944
Reference score
- Variants: 598
- Variants ignored: 9
-
Trait: Eczema, dermatitis
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 543 (90.8%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000945
Reference score
- Variants: 26
- Variants ignored: 0
-
Trait: Dementia in alzheimer's disease (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 22 (84.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000946
Reference score
- Variants: 9
- Variants ignored: 0
-
Trait: Unspecified dementia (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 8 (88.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000947
Reference score
- Variants: 1,648
- Variants ignored: 9
-
Trait: Mouth ulcers
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,522 (92.35%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000948
Reference score
- Variants: 1,899
- Variants ignored: 18
-
Trait: Inguinal hernia
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,668 (87.84%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000949
Reference score
- Variants: 3,085
- Variants ignored: 0
-
Trait: Inguinal hernia (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,801 (90.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000950
Reference score
- Variants: 169
- Variants ignored: 9
-
Trait: Skin changes due to chronic exposure to nonionising radiation (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 142 (84.02%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000951
Reference score
- Variants: 13,735
- Variants ignored: 18
-
Trait: Heel Broadband ultrasound attenuation, direct entry
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 13,002 (94.66%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000952
Reference score
- Variants: 14,311
- Variants ignored: 18
-
Trait: Heel quantitative ultrasound index (QUI), direct entry
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 13,568 (94.81%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000953
Reference score
- Variants: 7,688
- Variants ignored: 9
-
Trait: Left heel broadband ultrasound attenuation
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 7,220 (93.91%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000954
Reference score
- Variants: 9,272
- Variants ignored: 9
-
Trait: Left heel quantitative ultrasound index (QUI), direct entry
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 8,704 (93.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000955
Reference score
- Variants: 7,069
- Variants ignored: 0
-
Trait: Right heel broadband ultrasound attenuation
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 6,640 (93.93%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000956
Reference score
- Variants: 9,756
- Variants ignored: 0
-
Trait: Right heel quantitative ultrasound index (QUI), direct entry
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 9,171 (94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000957
Reference score
- Variants: 11,276
- Variants ignored: 9
-
Trait: Essential (primary hypertension) (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 10,685 (94.76%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000958
Reference score
- Variants: 9,400
- Variants ignored: 9
-
Trait: Essential hypertension
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 8,893 (94.61%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000959
Reference score
- Variants: 16
- Variants ignored: 18
-
Trait: Connective tissue disorder
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 12 (75%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000960
Reference score
- Variants: 79
- Variants ignored: 45
-
Trait: Other systemic involvement of connective tissue (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 66 (83.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000961
Reference score
- Variants: 1,143
- Variants ignored: 0
-
Trait: Phlebitis and thrombophlebitis (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,025 (89.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000962
Reference score
- Variants: 2,168
- Variants ignored: 18
-
Trait: Chronic ischaemic heart disease (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,960 (90.41%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000963
Reference score
- Variants: 264
- Variants ignored: 0
-
Trait: Follicular cysts of skin and subcutaneous tissue (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 230 (87.12%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000964
Reference score
- Variants: 47
- Variants ignored: 0
-
Trait: Slipped disc
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 40 (85.11%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000965
Reference score
- Variants: 4,535
- Variants ignored: 99
-
Trait: Hypothyroidism/myxoedema
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 4,319 (95.24%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000966
Reference score
- Variants: 1
- Variants ignored: 9
-
Trait: Iritis
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 0 (0%) zero
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000967
Reference score
- Variants: 634
- Variants ignored: 0
-
Trait: Coxarthrosis [arthrosis of hip] (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 573 (90.38%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000969
Reference score
- Variants: 36,345
- Variants ignored: 9
-
Trait: Sitting height
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 34,737 (95.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000972
Reference score
- Variants: 1,097
- Variants ignored: 0
-
Trait: Microalbumin [> 40 mg/L]
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 985 (89.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000976
Reference score
- Variants: 16
- Variants ignored: 0
-
Trait: JCV seropositivity for Human Polyomavirus JCV
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 9 (56.25%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000977
Reference score
- Variants: 3
- Variants ignored: 0
-
Trait: MCV seropositivity for Merkel Cell Polyomavirus
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2 (66.67%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000978
Reference score
- Variants: 3,483
- Variants ignored: 0
-
Trait: Bread intake
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3,195 (91.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000980
Reference score
- Variants: 2,594
- Variants ignored: 0
-
Trait: Use of sun / ultraviolet protection (always)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,414 (93.06%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000982
Reference score
- Variants: 1,141
- Variants ignored: 0
-
Trait: Use of sun / ultraviolet protection (never / rarely)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,004 (87.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000984
Reference score
- Variants: 5,774
- Variants ignored: 0
-
Trait: Frequency of playing computer games
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 5,425 (93.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000987
Reference score
- Variants: 13,277
- Variants ignored: 63
-
Trait: Mean reticulocyte volume
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 12,630 (95.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000988
Reference score
- Variants: 7,184
- Variants ignored: 0
-
Trait: High light scatter reticulocyte percentage
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 6,801 (94.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000989
Reference score
- Variants: 6,251
- Variants ignored: 0
-
Trait: Reticulocyte %
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 5,873 (93.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000990
Reference score
- Variants: 237
- Variants ignored: 0
-
Trait: Retinal detachments and breaks (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 204 (86.08%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000991
Reference score
- Variants: 2,816
- Variants ignored: 9
-
Trait: Never eat sugar
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,613 (92.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000993
Reference score
- Variants: 3,925
- Variants ignored: 0
-
Trait: Oily fish consumption
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3,655 (93.12%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000994
Reference score
- Variants: 3,119
- Variants ignored: 0
-
Trait: Tea intake
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,893 (92.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000995
Reference score
- Variants: 6,042
- Variants ignored: 0
-
Trait: Dentures
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 5,677 (93.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000996
Reference score
- Variants: 368
- Variants ignored: 0
-
Trait: Diverticular disease/diverticulitis
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 327 (88.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000997
Reference score
- Variants: 5,757
- Variants ignored: 36
-
Trait: Diverticular disease of intestine (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 5,392 (93.66%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000998
Reference score
- Variants: 24,144
- Variants ignored: 36
-
Trait: Comparative body height at age 10
- Mapped Trait(s):
- EFO_0009819: comparative body size at age 10, self-reported
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 23,017 (95.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS000999
Reference score
- Variants: 13,034
- Variants ignored: 9
-
Trait: Comparative body size at age 10
- Mapped Trait(s):
- EFO_0009819: comparative body size at age 10, self-reported
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 12,386 (95.03%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001000
Reference score
- Variants: 10,264
- Variants ignored: 0
-
Trait: Nap during day
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 9,676 (94.27%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001001
Reference score
- Variants: 7,743
- Variants ignored: 9
-
Trait: Getting up in morning
- Mapped Trait(s):
- EFO_0009817: ease of getting up in the morning, self-reported
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 7,330 (94.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001002
Reference score
- Variants: 35,046
- Variants ignored: 0
-
Trait: Whole body water mass
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 33,319 (95.07%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001003
Reference score
- Variants: 8,085
- Variants ignored: 36
-
Trait: Number of medications taken
- Mapped Trait(s):
- EFO_0009803: number of treatments or medications taken, self-reported
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 7,641 (94.51%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001004
Reference score
- Variants: 5,212
- Variants ignored: 27
-
Trait: Number of non-cancer illnesses
- Mapped Trait(s):
- EFO_0009801: number of non-cancer illnesses, self-reported
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 4,901 (94.03%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001005
Reference score
- Variants: 526
- Variants ignored: 0
-
Trait: Number of self reported cancers
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 476 (90.49%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001006
Reference score
- Variants: 2,638
- Variants ignored: 0
-
Trait: Weight change compared with 1 year ago
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,469 (93.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001007
Reference score
- Variants: 9,997
- Variants ignored: 0
-
Trait: Age at first sexual intercourse
- Mapped Trait(s):
- EFO_0009749: age at first sexual intercourse measurement
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 9,439 (94.42%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001008
Reference score
- Variants: 10,464
- Variants ignored: 18
-
Trait: Overall health rating
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 9,886 (94.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001009
Reference score
- Variants: 9,523
- Variants ignored: 18
-
Trait: PEF
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 8,965 (94.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001010
Reference score
- Variants: 15,135
- Variants ignored: 27
-
Trait: PEF pred. ratio
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 14,399 (95.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001011
Reference score
- Variants: 5
- Variants ignored: 0
-
Trait: Viral warts (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3 (60%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001012
Reference score
- Variants: 2,103
- Variants ignored: 18
-
Trait: Number of falls in the last year
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,940 (92.25%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001013
Reference score
- Variants: 53
- Variants ignored: 0
-
Trait: Macular degeneration
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 41 (77.36%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001014
Reference score
- Variants: 69
- Variants ignored: 9
-
Trait: Other disorders of pancreatic internal secretion (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 56 (81.16%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001015
Reference score
- Variants: 449
- Variants ignored: 9
-
Trait: Enlarged prostate
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 345 (76.84%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001016
Reference score
- Variants: 7,922
- Variants ignored: 9
-
Trait: Sensitivity / hurt feelings
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 7,436 (93.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001017
Reference score
- Variants: 3,348
- Variants ignored: 9
-
Trait: Suffer from 'nerves'
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3,115 (93.04%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001018
Reference score
- Variants: 2,912
- Variants ignored: 9
-
Trait: Attending social / leisure activities (attend any of the followings in once a week or more often: sports club, gym, pub, social club, religious group, adult edication class, or other group activity)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,697 (92.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001019
Reference score
- Variants: 11,361
- Variants ignored: 9
-
Trait: Attending social / leisure activities (regular attendance at a gym or sports club)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 10,746 (94.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001020
Reference score
- Variants: 220
- Variants ignored: 0
-
Trait: Attending social / leisure activities (regular attendance at an adult education class)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 206 (93.64%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001021
Reference score
- Variants: 9,747
- Variants ignored: 0
-
Trait: Feelings of worry or anxiety
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 9,189 (94.28%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001022
Reference score
- Variants: 7,714
- Variants ignored: 0
-
Trait: Worry too long after an embarrassing experience
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 7,253 (94.02%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001023
Reference score
- Variants: 2
- Variants ignored: 0
-
Trait: Disorders of mineral metabolism (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001024
Reference score
- Variants: 786
- Variants ignored: 18
-
Trait: Hemorrhoid
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 707 (89.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001025
Reference score
- Variants: 36
- Variants ignored: 0
-
Trait: Nonrheumatic aortic valve disorders (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 26 (72.22%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001026
Reference score
- Variants: 45
- Variants ignored: 0
-
Trait: Forearm or wrist fracture
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 40 (88.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001027
Reference score
- Variants: 118
- Variants ignored: 0
-
Trait: Internal derangement of knee (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 100 (84.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001028
Reference score
- Variants: 123
- Variants ignored: 18
-
Trait: Diabetic eye disease
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 97 (78.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001029
Reference score
- Variants: 22
- Variants ignored: 0
-
Trait: Other disorders of cornea (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 19 (86.36%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001030
Reference score
- Variants: 51
- Variants ignored: 0
-
Trait: Pulmonary fibrosis
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 42 (82.35%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001031
Reference score
- Variants: 252
- Variants ignored: 0
-
Trait: Fibroblastic disorders (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 208 (82.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001032
Reference score
- Variants: 161
- Variants ignored: 0
-
Trait: Uterine fibroids
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 152 (94.41%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001033
Reference score
- Variants: 1
- Variants ignored: 0
-
Trait: Other coagulation defects (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001034
Reference score
- Variants: 6,651
- Variants ignored: 0
-
Trait: Salt added to food
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 6,278 (94.39%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001036
Reference score
- Variants: 38
- Variants ignored: 27
-
Trait: Epstein Barr virus nuclear antigen 1 IgG seropositivity
- Mapped Trait(s):
- EFO_0009271: Epstein Barr virus nuclear antigen-1 seropositivity
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 31 (81.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001037
Reference score
- Variants: 14,310
- Variants ignored: 18
-
Trait: Heel bone mineral density (BMD) T-score, automated
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 13,566 (94.8%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001038
Reference score
- Variants: 9,275
- Variants ignored: 9
-
Trait: Left heel bone mineral density (BMD) T-score, automated
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 8,707 (93.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001039
Reference score
- Variants: 9,753
- Variants ignored: 0
-
Trait: Right heel bone mineral density (BMD) T-score, automated
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 9,169 (94.01%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001040
Reference score
- Variants: 1,610
- Variants ignored: 9
-
Trait: Non melanoma skin cancer
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,483 (92.11%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001041
Reference score
- Variants: 1,298
- Variants ignored: 9
-
Trait: Skin cancer
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,184 (91.22%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001042
Reference score
- Variants: 226
- Variants ignored: 45
-
Trait: Thyrotoxicosis [hyperthyroidism] (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 210 (92.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001043
Reference score
- Variants: 69
- Variants ignored: 45
-
Trait: Hyperthyroidism, thyrotoxicosis
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 60 (86.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001044
Reference score
- Variants: 324
- Variants ignored: 0
-
Trait: Glucosamine intake
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 291 (89.81%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001045
Reference score
- Variants: 5
- Variants ignored: 18
-
Trait: Vitamin B9 intake
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3 (60%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001046
Reference score
- Variants: 6,169
- Variants ignored: 0
-
Trait: Past tobacco smoking (Smoked at least once)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 5,793 (93.91%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001047
Reference score
- Variants: 2,245
- Variants ignored: 0
-
Trait: Past tobacco smoking (Smoked occasionally)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,075 (92.43%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001048
Reference score
- Variants: 687
- Variants ignored: 0
-
Trait: NSTEMI (algorithmically-defined)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 586 (85.3%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001049
Reference score
- Variants: 4,299
- Variants ignored: 18
-
Trait: Risk taking behaviour
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 4,012 (93.32%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001050
Reference score
- Variants: 1,857
- Variants ignored: 0
-
Trait: Diaphragmatic hernia (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,722 (92.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001051
Reference score
- Variants: 69
- Variants ignored: 45
-
Trait: Polymyalgia rheumatica
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 56 (81.16%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001052
Reference score
- Variants: 5,661
- Variants ignored: 0
-
Trait: Time spend outdoors in summer
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 5,270 (93.09%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001053
Reference score
- Variants: 2,323
- Variants ignored: 0
-
Trait: Time spend outdoors in winter
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,104 (90.57%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001054
Reference score
- Variants: 7,407
- Variants ignored: 27
-
Trait: Snoring
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 6,909 (93.28%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001055
Reference score
- Variants: 11,428
- Variants ignored: 0
-
Trait: Chronotype (morning/evening person)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 10,823 (94.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001056
Reference score
- Variants: 991
- Variants ignored: 0
-
Trait: Beef intake
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 919 (92.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001057
Reference score
- Variants: 4,882
- Variants ignored: 9
-
Trait: Cereal consumption
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 4,593 (94.08%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001058
Reference score
- Variants: 146
- Variants ignored: 0
-
Trait: Cereal consumption (biscuit cereal)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 127 (86.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001059
Reference score
- Variants: 1,286
- Variants ignored: 9
-
Trait: Cereal consumption (other)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,180 (91.76%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001060
Reference score
- Variants: 6,678
- Variants ignored: 0
-
Trait: Cheese intake
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 6,312 (94.52%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001061
Reference score
- Variants: 1,085
- Variants ignored: 0
-
Trait: Cooked vegetable consumption
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 968 (89.22%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001062
Reference score
- Variants: 4,257
- Variants ignored: 0
-
Trait: Fresh fruit intake
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3,986 (93.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001063
Reference score
- Variants: 730
- Variants ignored: 9
-
Trait: Major dietary changes in the last 5 years due to illness
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 644 (88.22%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001064
Reference score
- Variants: 116
- Variants ignored: 0
-
Trait: Milk consumption (skimmed)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 103 (88.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001065
Reference score
- Variants: 5
- Variants ignored: 9
-
Trait: Never eat wheat
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3 (60%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001066
Reference score
- Variants: 1,609
- Variants ignored: 0
-
Trait: Poultry intake
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,488 (92.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001067
Reference score
- Variants: 2,346
- Variants ignored: 0
-
Trait: Processed meat intake
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,154 (91.82%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001068
Reference score
- Variants: 1,353
- Variants ignored: 0
-
Trait: Variation in diet
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,244 (91.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001069
Reference score
- Variants: 4,994
- Variants ignored: 9
-
Trait: Water intake
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 4,676 (93.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001070
Reference score
- Variants: 880
- Variants ignored: 0
-
Trait: Volume of ventricular cerebrospinal fluid (normalised for head size)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 789 (89.66%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001071
Reference score
- Variants: 6,782
- Variants ignored: 0
-
Trait: Facial aging, looking 'about your age'
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 6,368 (93.9%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001072
Reference score
- Variants: 39
- Variants ignored: 0
-
Trait: Facial aging, looking 'older than you are'
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 30 (76.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001073
Reference score
- Variants: 1,323
- Variants ignored: 0
-
Trait: Duration of walks
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,205 (91.08%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001074
Reference score
- Variants: 3,846
- Variants ignored: 9
-
Trait: Types of physical activity in last 4 weeks (other exercises)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3,588 (93.29%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001075
Reference score
- Variants: 7,535
- Variants ignored: 36
-
Trait: Usual walking pace
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 7,089 (94.08%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001076
Reference score
- Variants: 12,563
- Variants ignored: 63
-
Trait: Eosinophill %
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 11,915 (94.84%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001077
Reference score
- Variants: 13,703
- Variants ignored: 63
-
Trait: Neutrophill %
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 13,032 (95.1%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001078
Reference score
- Variants: 8,762
- Variants ignored: 18
-
Trait: Monocyte %
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 8,292 (94.64%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001079
Reference score
- Variants: 18,814
- Variants ignored: 0
-
Trait: Platelet distribution width
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 17,858 (94.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001080
Reference score
- Variants: 5,594
- Variants ignored: 9
-
Trait: Freq. of tiredness / lethargy in last 2 weeks
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 5,279 (94.37%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001081
Reference score
- Variants: 9
- Variants ignored: 0
-
Trait: JC VP1 antigen for Human Polyomavirus JCV
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 7 (77.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001082
Reference score
- Variants: 143
- Variants ignored: 9
-
Trait: MC VP1 antigen for Merkel Cell Polyomavirus
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 126 (88.11%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001085
Reference score
- Variants: 214
- Variants ignored: 0
-
Trait: Increased alcohol consumption, versus 10 years ago
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 191 (89.25%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001086
Reference score
- Variants: 1,028
- Variants ignored: 9
-
Trait: Alcohol consumption
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 917 (89.2%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001087
Reference score
- Variants: 8,353
- Variants ignored: 0
-
Trait: Alcohol intake frequency
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 7,849 (93.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001088
Reference score
- Variants: 2,842
- Variants ignored: 18
-
Trait: Average weekly alcohol consumption (beer and cider)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,517 (88.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001090
Reference score
- Variants: 7,555
- Variants ignored: 0
-
Trait: Often felt loved as a child
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 7,087 (93.81%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001091
Reference score
- Variants: 660
- Variants ignored: 18
-
Trait: Loneliness
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 585 (88.64%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001092
Reference score
- Variants: 1,649
- Variants ignored: 0
-
Trait: Hair colour, black
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,461 (88.6%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001093
Reference score
- Variants: 6,970
- Variants ignored: 18
-
Trait: Hair colour, blonde
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 6,609 (94.82%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001094
Reference score
- Variants: 4,024
- Variants ignored: 0
-
Trait: Hair colour, brown
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3,756 (93.34%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001095
Reference score
- Variants: 5,662
- Variants ignored: 0
-
Trait: Hair colour, dark brown
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 5,334 (94.21%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001096
Reference score
- Variants: 2,127
- Variants ignored: 0
-
Trait: Hair colour, light brown
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,969 (92.57%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001097
Reference score
- Variants: 21
- Variants ignored: 0
-
Trait: Hair colour, other
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 16 (76.19%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001098
Reference score
- Variants: 1,621
- Variants ignored: 0
-
Trait: Hair colour, red
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,494 (92.17%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001099
Reference score
- Variants: 6,639
- Variants ignored: 9
-
Trait: Spherical power (left eye)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 6,284 (94.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001100
Reference score
- Variants: 7,350
- Variants ignored: 9
-
Trait: Spherical power (right eye)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 6,993 (95.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001101
Reference score
- Variants: 27,396
- Variants ignored: 27
-
Trait: Body fat percentage
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 26,158 (95.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001102
Reference score
- Variants: 25,266
- Variants ignored: 9
-
Trait: Body fat percentage (left arm)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 24,236 (95.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001103
Reference score
- Variants: 28,134
- Variants ignored: 9
-
Trait: Body fat percentage (left leg)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 26,854 (95.45%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001104
Reference score
- Variants: 28,163
- Variants ignored: 9
-
Trait: Body fat percentage (right leg)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 26,853 (95.35%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001105
Reference score
- Variants: 25,651
- Variants ignored: 18
-
Trait: Body fat percentage (trunk fat)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 24,492 (95.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001106
Reference score
- Variants: 23,943
- Variants ignored: 9
-
Trait: Percentage of right arm fat
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 23,035 (96.21%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001107
Reference score
- Variants: 1,040
- Variants ignored: 0
-
Trait: UACR [> 30 mg/g]
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 928 (89.23%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001108
Reference score
- Variants: 32,154
- Variants ignored: 0
-
Trait: Basal metabolic rate
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 30,556 (95.03%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001109
Reference score
- Variants: 1,910
- Variants ignored: 27
-
Trait: Vasomotor and allergic rhinitis (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,753 (91.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001110
Reference score
- Variants: 6
- Variants ignored: 9
-
Trait: Reactive arthropathies (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 4 (66.67%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001111
Reference score
- Variants: 313
- Variants ignored: 18
-
Trait: Male genital tract cancer
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 224 (71.57%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001112
Reference score
- Variants: 499
- Variants ignored: 0
-
Trait: Aspirin
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 436 (87.37%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001113
Reference score
- Variants: 790
- Variants ignored: 9
-
Trait: Aspirin use self-reported
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 700 (88.61%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001114
Reference score
- Variants: 419
- Variants ignored: 0
-
Trait: Ibuprofen use self-reported
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 380 (90.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001115
Reference score
- Variants: 4,673
- Variants ignored: 18
-
Trait: Paracetamol use self-reported
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 4,399 (94.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001116
Reference score
- Variants: 174
- Variants ignored: 0
-
Trait: Ibuprofen (e.g. Nurofen)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 158 (90.8%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001117
Reference score
- Variants: 68
- Variants ignored: 27
-
Trait: Started insulin within one year diagnosis of diabetes
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 55 (80.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001118
Reference score
- Variants: 1,846
- Variants ignored: 9
-
Trait: Taking other prescription medications
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,712 (92.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001119
Reference score
- Variants: 13,767
- Variants ignored: 9
-
Trait: Left hand grip strength
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 12,944 (94.02%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001120
Reference score
- Variants: 12,644
- Variants ignored: 27
-
Trait: Right hand grip strength
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 11,899 (94.11%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001123
Reference score
- Variants: 48
- Variants ignored: 0
-
Trait: Coffee consumption
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 37 (77.08%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001124
Reference score
- Variants: 9,694
- Variants ignored: 0
-
Trait: Coffee consumption (ground coffee)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 9,095 (93.82%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001125
Reference score
- Variants: 432
- Variants ignored: 0
-
Trait: Coffee consumption (instant coffee)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 376 (87.04%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001126
Reference score
- Variants: 3,154
- Variants ignored: 0
-
Trait: Coffee intake
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,925 (92.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001127
Reference score
- Variants: 12,310
- Variants ignored: 0
-
Trait: Never Smoker
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 11,661 (94.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001128
Reference score
- Variants: 4,348
- Variants ignored: 0
-
Trait: Previous Smoker
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 4,074 (93.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001129
Reference score
- Variants: 974
- Variants ignored: 0
-
Trait: Smoking status (ever vs never smokers)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 886 (90.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001130
Reference score
- Variants: 725
- Variants ignored: 0
-
Trait: Number of cigarettes previously smoked per day
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 634 (87.45%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001131
Reference score
- Variants: 82
- Variants ignored: 9
-
Trait: Zoster [herpes zoster] (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 70 (85.37%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001132
Reference score
- Variants: 1,530
- Variants ignored: 9
-
Trait: Family history of chronic bronchitis/emphysema
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,402 (91.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001133
Reference score
- Variants: 14,103
- Variants ignored: 18
-
Trait: Diastolic BP (AR)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 13,425 (95.19%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001134
Reference score
- Variants: 15,481
- Variants ignored: 0
-
Trait: Systolic BP (AR)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 14,773 (95.43%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001135
Reference score
- Variants: 1,028
- Variants ignored: 18
-
Trait: Arthritis (nos)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 937 (91.15%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001136
Reference score
- Variants: 30
- Variants ignored: 0
-
Trait: Hematologic disease, genetic
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 23 (76.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001137
Reference score
- Variants: 321
- Variants ignored: 0
-
Trait: Retinal detachment
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 266 (82.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001138
Reference score
- Variants: 456
- Variants ignored: 18
-
Trait: Rheumatoid factor [> 16 IU/mL]
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 419 (91.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001139
Reference score
- Variants: 11
- Variants ignored: 0
-
Trait: Light smokers, at least 100 smokes in lifetime
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 8 (72.73%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001140
Reference score
- Variants: 1,368
- Variants ignored: 9
-
Trait: Seborrheic keratosis (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,245 (91.01%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001141
Reference score
- Variants: 7,676
- Variants ignored: 0
-
Trait: Facial ageing (looking younger than you are)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 7,238 (94.29%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001142
Reference score
- Variants: 2,215
- Variants ignored: 9
-
Trait: Volume of grey matter in Intracalcarine Cortex (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,057 (92.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001143
Reference score
- Variants: 699
- Variants ignored: 0
-
Trait: Volume of grey matter in Parietal Operculum Cortex (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 623 (89.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001144
Reference score
- Variants: 23,676
- Variants ignored: 9
-
Trait: Arm fat mass (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 22,697 (95.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001145
Reference score
- Variants: 23,528
- Variants ignored: 9
-
Trait: Arm fat mass (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 22,555 (95.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001146
Reference score
- Variants: 29,063
- Variants ignored: 0
-
Trait: Arm fat-free mass (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 27,537 (94.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001147
Reference score
- Variants: 23,565
- Variants ignored: 9
-
Trait: Leg fat mass (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 22,578 (95.81%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001148
Reference score
- Variants: 29,233
- Variants ignored: 9
-
Trait: Trunk fat mass
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 27,914 (95.49%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001149
Reference score
- Variants: 27,550
- Variants ignored: 0
-
Trait: Whole body fat mass
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 26,333 (95.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001150
Reference score
- Variants: 4,106
- Variants ignored: 0
-
Trait: Sleep duration
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3,882 (94.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001152
Reference score
- Variants: 10,179
- Variants ignored: 18
-
Trait: Red blood cell distribution width
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 9,624 (94.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001153
Reference score
- Variants: 5
- Variants ignored: 18
-
Trait: Folic acid or folate (Vitamin B9)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3 (60%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001154
Reference score
- Variants: 26,740
- Variants ignored: 0
-
Trait: Impedance (left arm)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 25,611 (95.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001155
Reference score
- Variants: 28,999
- Variants ignored: 18
-
Trait: Impedance (left leg)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 27,752 (95.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001156
Reference score
- Variants: 30,140
- Variants ignored: 18
-
Trait: Impedance (right arm)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 28,848 (95.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001157
Reference score
- Variants: 30,300
- Variants ignored: 18
-
Trait: Impedance (right leg)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 28,998 (95.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001158
Reference score
- Variants: 30,421
- Variants ignored: 0
-
Trait: Left leg mass (predicted)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 28,900 (95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001159
Reference score
- Variants: 32,103
- Variants ignored: 0
-
Trait: Right leg mass (predicted)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 30,497 (95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001160
Reference score
- Variants: 32,685
- Variants ignored: 0
-
Trait: Trunk mass (predicted)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 31,039 (94.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001161
Reference score
- Variants: 32,218
- Variants ignored: 18
-
Trait: Whole body impedance
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 30,807 (95.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001162
Reference score
- Variants: 24,605
- Variants ignored: 0
-
Trait: Hip circumference
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 23,555 (95.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001163
Reference score
- Variants: 9,323
- Variants ignored: 27
-
Trait: Monocyte count
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 8,831 (94.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001164
Reference score
- Variants: 280
- Variants ignored: 0
-
Trait: Testicular cancer
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 201 (71.79%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001165
Reference score
- Variants: 30,360
- Variants ignored: 9
-
Trait: Arm fat free mass (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 28,773 (94.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001166
Reference score
- Variants: 30,340
- Variants ignored: 0
-
Trait: Leg fat free mass (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 28,824 (95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001167
Reference score
- Variants: 32,046
- Variants ignored: 0
-
Trait: Leg fat-free mass (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 30,454 (95.03%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001168
Reference score
- Variants: 34,749
- Variants ignored: 0
-
Trait: Trunk fat free mass
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 33,012 (95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001169
Reference score
- Variants: 34,486
- Variants ignored: 0
-
Trait: Whole body fat free mass
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 32,772 (95.03%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001172
Reference score
- Variants: 12,579
- Variants ignored: 54
-
Trait: Eosinophill count
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 11,919 (94.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001173
Reference score
- Variants: 15,578
- Variants ignored: 18
-
Trait: Neutrophill count
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 14,815 (95.1%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001174
Reference score
- Variants: 970
- Variants ignored: 0
-
Trait: Cholelithiasis (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 907 (93.51%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001179
Reference score
- Variants: 7
- Variants ignored: 0
-
Trait: Vascular dementia (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 5 (71.43%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001180
Reference score
- Variants: 15,141
- Variants ignored: 27
-
Trait: Lung function (FEV1/FVC)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 14,405 (95.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001181
Reference score
- Variants: 4,739
- Variants ignored: 90
-
Trait: Other hypothyroidism (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 4,507 (95.1%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001182
Reference score
- Variants: 351
- Variants ignored: 0
-
Trait: Estradiol [> 212 pmol/L]
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 316 (90.03%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001185
Reference score
- Variants: 3,584
- Variants ignored: 0
-
Trait: Intra-ocular pressure, Goldmann-correlated ®
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3,317 (92.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001192
Reference score
- Variants: 4,525
- Variants ignored: 0
-
Trait: Gonarthrosis [arthrosis of knee] (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 4,202 (92.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001199
Reference score
- Variants: 4,212
- Variants ignored: 45
-
Trait: Lymphocyte count
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3,920 (93.07%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001200
Reference score
- Variants: 24,114
- Variants ignored: 45
-
Trait: Mean platelet volume
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 22,959 (95.21%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001218
Reference score
- Variants: 2,359
- Variants ignored: 0
-
Trait: Mean corpuscular haemoglobin concentration
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,201 (93.3%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001219
Reference score
- Variants: 13,003
- Variants ignored: 36
-
Trait: Mean corpuscular hemoglobin
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 12,361 (95.06%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001220
Reference score
- Variants: 17,311
- Variants ignored: 18
-
Trait: Mean corpuscular volume
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 16,512 (95.38%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001225
Reference score
- Variants: 15,721
- Variants ignored: 27
-
Trait: Percentage of hematocrit
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 14,902 (94.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001226
Reference score
- Variants: 6,278
- Variants ignored: 18
-
Trait: Birth weight
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 5,936 (94.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001227
Reference score
- Variants: 25,538
- Variants ignored: 9
-
Trait: Waist circumference
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 24,367 (95.41%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001228
Reference score
- Variants: 27,126
- Variants ignored: 9
-
Trait: Body mass index
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 25,927 (95.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001229
Reference score
- Variants: 51,209
- Variants ignored: 36
-
Trait: Standing height
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 48,952 (95.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001230
Reference score
- Variants: 31,222
- Variants ignored: 9
-
Trait: Body weight
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 29,790 (95.41%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001232
Reference score
- Variants: 10,055
- Variants ignored: 0
-
Trait: Fluid intelligence score
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 9,517 (94.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001233
Reference score
- Variants: 14,455
- Variants ignored: 0
-
Trait: Heart rate (AR)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 13,709 (94.84%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001234
Reference score
- Variants: 30,666
- Variants ignored: 0
-
Trait: Left arm mass (predicted)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 29,066 (94.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001235
Reference score
- Variants: 28,988
- Variants ignored: 0
-
Trait: Right arm mass (predicted)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 27,460 (94.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001236
Reference score
- Variants: 17,732
- Variants ignored: 9
-
Trait: Lung function (FEV1)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 16,790 (94.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001237
Reference score
- Variants: 20,921
- Variants ignored: 18
-
Trait: Lung function (FVC)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 19,833 (94.8%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001238
Reference score
- Variants: 24,893
- Variants ignored: 27
-
Trait: Platelet count
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 23,770 (95.49%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001239
Reference score
- Variants: 13,785
- Variants ignored: 27
-
Trait: White blood cell count
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 13,122 (95.19%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001240
Reference score
- Variants: 20,480
- Variants ignored: 45
-
Trait: Red blood cell count
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 19,447 (94.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001241
Reference score
- Variants: 21,694
- Variants ignored: 0
-
Trait: Ankle spacing width
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 20,650 (95.19%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001242
Reference score
- Variants: 13,416
- Variants ignored: 27
-
Trait: Ankle spacing width (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 12,671 (94.45%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001243
Reference score
- Variants: 15,134
- Variants ignored: 18
-
Trait: Ankle spacing width (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 14,322 (94.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001244
Reference score
- Variants: 958
- Variants ignored: 0
-
Trait: Ease of skin tanning (get mildly or occasionally tanned)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 887 (92.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001245
Reference score
- Variants: 2,693
- Variants ignored: 0
-
Trait: Ease of skin tanning (get moderately tanned)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,503 (92.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001246
Reference score
- Variants: 4,130
- Variants ignored: 0
-
Trait: Ease of skin tanning (get very tanned)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3,849 (93.2%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001247
Reference score
- Variants: 3,159
- Variants ignored: 9
-
Trait: Ease of skin tanning (never tan, only burn)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,959 (93.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001248
Reference score
- Variants: 880
- Variants ignored: 0
-
Trait: Gout
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 732 (83.18%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001249
Reference score
- Variants: 1,796
- Variants ignored: 0
-
Trait: Gout (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,555 (86.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001250
Reference score
- Variants: 341
- Variants ignored: 0
-
Trait: Calculus of kidney and ureter (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 282 (82.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001251
Reference score
- Variants: 57
- Variants ignored: 0
-
Trait: Other interstitial pulmonary diseases (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 48 (84.21%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001252
Reference score
- Variants: 3,731
- Variants ignored: 0
-
Trait: Hearing difficulty and deafness
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3,443 (92.28%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001253
Reference score
- Variants: 3,098
- Variants ignored: 0
-
Trait: Hearing difficulty
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,845 (91.83%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001254
Reference score
- Variants: 11
- Variants ignored: 0
-
Trait: Dupuytren's contracture
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 8 (72.73%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001255
Reference score
- Variants: 213
- Variants ignored: 0
-
Trait: Otosclerosis (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 192 (90.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001256
Reference score
- Variants: 876
- Variants ignored: 0
-
Trait: Gallstones
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 824 (94.06%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001257
Reference score
- Variants: 519
- Variants ignored: 0
-
Trait: Childhood sunburn
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 472 (90.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001258
Reference score
- Variants: 365
- Variants ignored: 0
-
Trait: Radius fracture
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 332 (90.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001259
Reference score
- Variants: 349
- Variants ignored: 9
-
Trait: Hayfever/allergic rhinitis
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 311 (89.11%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001260
Reference score
- Variants: 2,562
- Variants ignored: 9
-
Trait: Angina
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,333 (91.06%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001261
Reference score
- Variants: 2,524
- Variants ignored: 0
-
Trait: Angina pectoris (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,307 (91.4%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001262
Reference score
- Variants: 1,852
- Variants ignored: 9
-
Trait: Vascular/heart problems diagnosed by doctor Angina
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,678 (90.6%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001263
Reference score
- Variants: 2,087
- Variants ignored: 0
-
Trait: Atrial flutter
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,914 (91.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001264
Reference score
- Variants: 839
- Variants ignored: 0
-
Trait: Deep vein thrombosis
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 746 (88.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001265
Reference score
- Variants: 1,530
- Variants ignored: 0
-
Trait: Deep vein thrombosis (leg)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,391 (90.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001266
Reference score
- Variants: 1,773
- Variants ignored: 0
-
Trait: Deep vein thrombosis (diagnosed by doctor)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,623 (91.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001267
Reference score
- Variants: 10
- Variants ignored: 9
-
Trait: Ankylosing spondylitis
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 9 (90%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001268
Reference score
- Variants: 10
- Variants ignored: 9
-
Trait: Ankylosing spondylitis (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 9 (90%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001270
Reference score
- Variants: 41
- Variants ignored: 18
-
Trait: Multiple sclerosis
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 36 (87.8%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001271
Reference score
- Variants: 36
- Variants ignored: 18
-
Trait: Multiple sclerosis (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 31 (86.11%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001272
Reference score
- Variants: 158
- Variants ignored: 0
-
Trait: Chronic renal failure (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 136 (86.08%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001273
Reference score
- Variants: 316
- Variants ignored: 0
-
Trait: Osteoporosis
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 289 (91.46%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001274
Reference score
- Variants: 1,270
- Variants ignored: 0
-
Trait: Osteoporosis without pathological fracture (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,202 (94.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001275
Reference score
- Variants: 6
- Variants ignored: 0
-
Trait: Other retinal disorders (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 5 (83.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001276
Reference score
- Variants: 185
- Variants ignored: 18
-
Trait: Retinal disorders in diseases classified elsewhere (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 150 (81.08%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001277
Reference score
- Variants: 96
- Variants ignored: 0
-
Trait: PE +/- DVT
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 78 (81.25%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001278
Reference score
- Variants: 551
- Variants ignored: 0
-
Trait: previously: Blood clot in the leg (DVT) or lung
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 493 (89.47%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001279
Reference score
- Variants: 94
- Variants ignored: 0
-
Trait: previously: Blood clot in the lung
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 79 (84.04%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001280
Reference score
- Variants: 88
- Variants ignored: 0
-
Trait: PE (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 69 (78.41%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001281
Reference score
- Variants: 25
- Variants ignored: 0
-
Trait: Migraine
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 24 (96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001282
Reference score
- Variants: 329
- Variants ignored: 0
-
Trait: Migraine (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 300 (91.19%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001283
Reference score
- Variants: 993
- Variants ignored: 18
-
Trait: Allergic disease (hay fever, rhinitis or eczema)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 896 (90.23%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001284
Reference score
- Variants: 6,755
- Variants ignored: 54
-
Trait: Allergic disease (hay fever, allergic rhinitis, or eczema)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 6,384 (94.51%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001285
Reference score
- Variants: 7,313
- Variants ignored: 54
-
Trait: Allergic disease (hay fever, rhinitis, or eczema) (diagnosed by doctor)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 6,926 (94.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001286
Reference score
- Variants: 466
- Variants ignored: 0
-
Trait: Allergic disease (hay fever or allergic rhinitis) (diagnosed by doctor)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 414 (88.84%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001287
Reference score
- Variants: 36
- Variants ignored: 27
-
Trait: Psoriatic arthropathy
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 26 (72.22%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001288
Reference score
- Variants: 195
- Variants ignored: 18
-
Trait: Inflammatory bowel disease
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 170 (87.18%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001289
Reference score
- Variants: 11
- Variants ignored: 0
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 8 (72.73%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001290
Reference score
- Variants: 579
- Variants ignored: 0
-
Trait: Osteoarthritis
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 534 (92.23%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001291
Reference score
- Variants: 948
- Variants ignored: 9
-
Trait: Prostate cancer
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 795 (83.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001292
Reference score
- Variants: 602
- Variants ignored: 9
-
Trait: Family history of prostate cancer
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 542 (90.03%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001293
Reference score
- Variants: 92
- Variants ignored: 0
-
Trait: Other diseases of liver (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 79 (85.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001294
Reference score
- Variants: 3,496
- Variants ignored: 36
-
Trait: Non-insulin-dependent diabetes (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3,217 (92.02%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001295
Reference score
- Variants: 385
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 325 (84.42%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001296
Reference score
- Variants: 356
- Variants ignored: 36
-
Trait: Insulin-dependent diabetes mellitus (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 305 (85.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001297
Reference score
- Variants: 69
- Variants ignored: 27
-
Trait: Type 1 diabetes
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 57 (82.61%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001298
Reference score
- Variants: 9,227
- Variants ignored: 0
-
Trait: Obesity (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 8,700 (94.29%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001299
Reference score
- Variants: 24
- Variants ignored: 9
-
Trait: Cervical cancer
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 20 (83.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001300
Reference score
- Variants: 9
- Variants ignored: 18
-
Trait: Celiac disease or gluten sensitivity, diagnosed
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 4 (44.44%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001301
Reference score
- Variants: 428
- Variants ignored: 45
-
Trait: Malabsorption/coeliac disease
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 378 (88.32%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001302
Reference score
- Variants: 1,214
- Variants ignored: 0
-
Trait: Cataract
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,110 (91.43%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001303
Reference score
- Variants: 480
- Variants ignored: 0
-
Trait: Other cataract (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 434 (90.42%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001304
Reference score
- Variants: 116
- Variants ignored: 0
-
Trait: Melanoma (malignant)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 104 (89.66%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001305
Reference score
- Variants: 121
- Variants ignored: 0
-
Trait: Vitamin b12 deficiency induced anemia (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 104 (85.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001306
Reference score
- Variants: 179
- Variants ignored: 27
-
Trait: Ulcerative colitis
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 154 (86.03%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001307
Reference score
- Variants: 809
- Variants ignored: 27
-
Trait: Ulcerative colitis (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 703 (86.9%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001308
Reference score
- Variants: 7
- Variants ignored: 0
-
Trait: Sjogren's syndrome/sicca syndrome
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 7 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001309
Reference score
- Variants: 323
- Variants ignored: 18
-
Trait: Other rheumatoid arthritis (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 285 (88.24%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001310
Reference score
- Variants: 175
- Variants ignored: 27
-
Trait: Rheumatoid arthritis
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 147 (84%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001311
Reference score
- Variants: 3
- Variants ignored: 9
-
Trait: Seropositive rheumatoid arthritis (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2 (66.67%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001312
Reference score
- Variants: 204
- Variants ignored: 36
-
Trait: Psoriasis
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 179 (87.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001313
Reference score
- Variants: 578
- Variants ignored: 36
-
Trait: Psoriasis (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 530 (91.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001314
Reference score
- Variants: 1,108
- Variants ignored: 0
-
Trait: Acute myocardial infarction (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 971 (87.64%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001315
Reference score
- Variants: 1,788
- Variants ignored: 0
-
Trait: Myocardial infarction
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,608 (89.93%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001316
Reference score
- Variants: 1,831
- Variants ignored: 0
-
Trait: Myocardial infarction (algorithmically-defined)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,650 (90.11%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001317
Reference score
- Variants: 1,030
- Variants ignored: 9
-
Trait: Vascular/heart problems diagnosed by doctor Heart attack
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 887 (86.12%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001318
Reference score
- Variants: 7,845
- Variants ignored: 18
-
Trait: Disorders of lipoprotein metabolism and other lipidaemias (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 7,357 (93.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001319
Reference score
- Variants: 2
- Variants ignored: 0
-
Trait: Other metabolic disorders (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001320
Reference score
- Variants: 13,791
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 13,127 (95.19%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001321
Reference score
- Variants: 1,103
- Variants ignored: 0
-
Trait: Eye problems/disorders (Glaucoma)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 992 (89.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001322
Reference score
- Variants: 655
- Variants ignored: 0
-
Trait: Glaucoma
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 596 (90.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001323
Reference score
- Variants: 2,066
- Variants ignored: 0
-
Trait: Glaucoma (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,874 (90.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001324
Reference score
- Variants: 13,862
- Variants ignored: 18
-
Trait: Family history of high blood pressure
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 13,144 (94.82%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001326
Reference score
- Variants: 42
- Variants ignored: 0
-
Trait: Emphysema
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 34 (80.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001327
Reference score
- Variants: 4,053
- Variants ignored: 18
-
Trait: Diabetes
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3,741 (92.3%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001328
Reference score
- Variants: 2,515
- Variants ignored: 18
-
Trait: Family history of diabetes
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,333 (92.76%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001329
Reference score
- Variants: 2,270
- Variants ignored: 27
-
Trait: Unspecified diabetes mellitus (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,072 (91.28%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001330
Reference score
- Variants: 220
- Variants ignored: 9
-
Trait: Crohn's disease [regional enteritis] (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 192 (87.27%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001331
Reference score
- Variants: 257
- Variants ignored: 9
-
Trait: Crohns disease
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 226 (87.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001332
Reference score
- Variants: 482
- Variants ignored: 0
-
Trait: Chronic obstructive pulmonary disease
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 412 (85.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001333
Reference score
- Variants: 569
- Variants ignored: 9
-
Trait: Chronic obstructive pulmonary disease (algorithmically-defined)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 497 (87.35%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001334
Reference score
- Variants: 498
- Variants ignored: 0
-
Trait: Other chronic obstructive pulmonary disease (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 430 (86.35%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001335
Reference score
- Variants: 14,076
- Variants ignored: 9
-
Trait: Vascular/heart problems diagnosed by doctor High BP
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 13,352 (94.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001336
Reference score
- Variants: 555
- Variants ignored: 0
-
Trait: Breast cancer
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 518 (93.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001337
Reference score
- Variants: 195
- Variants ignored: 0
-
Trait: Family history of breast cancer
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 172 (88.21%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001338
Reference score
- Variants: 1,223
- Variants ignored: 9
-
Trait: Hyperplasia of prostate (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,026 (83.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001339
Reference score
- Variants: 2,142
- Variants ignored: 0
-
Trait: Atrial fibrillation and flutter (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,961 (91.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001340
Reference score
- Variants: 2,955
- Variants ignored: 0
-
Trait: Atrial fibrillation
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,742 (92.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001341
Reference score
- Variants: 6,430
- Variants ignored: 36
-
Trait: Asthma
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 6,067 (94.35%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001343
Reference score
- Variants: 6,425
- Variants ignored: 36
-
Trait: Asthma (algorithmically-defined)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 6,068 (94.44%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001344
Reference score
- Variants: 6,139
- Variants ignored: 45
-
Trait: Asthma (diagnosed by doctor)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 5,801 (94.49%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001345
Reference score
- Variants: 435
- Variants ignored: 27
-
Trait: Asthma (diagnosed by doctor)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 387 (88.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001346
Reference score
- Variants: 8,508
- Variants ignored: 36
-
Trait: Asthma (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 8,034 (94.43%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001347
Reference score
- Variants: 139
- Variants ignored: 0
-
Trait: Family history of Alzheimer's/dementia
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 119 (85.61%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001348
Reference score
- Variants: 15
- Variants ignored: 0
-
Trait: Alzheimer's disease (algorithmically-defined)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 12 (80%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001349
Reference score
- Variants: 6
- Variants ignored: 0
-
Trait: Alzheimer's disease (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 6 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001350
Reference score
- Variants: 1,023,373
- Variants ignored: 0
-
Trait: Fasting glucose
- Mapped Trait(s):
- Samples: 200,622
- Population:
- Publication: Chen J et.al, Nat Genet (2021-05-31)
- View in PGS-Catalog
Target study
- Coverage: 1,023,373 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001351
Reference score
- Variants: 1,025,098
- Variants ignored: 0
-
Trait: Fasting insulin
- Mapped Trait(s):
- Samples: 151,013
- Population:
- Publication: Chen J et.al, Nat Genet (2021-05-31)
- View in PGS-Catalog
Target study
- Coverage: 1,025,098 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001352
Reference score
- Variants: 1,018,836
- Variants ignored: 0
-
Trait: Glycated haemoglobin levels (HbA1c)
- Mapped Trait(s):
- Samples: 146,806
- Population:
- Publication: Chen J et.al, Nat Genet (2021-05-31)
- View in PGS-Catalog
Target study
- Coverage: 1,018,836 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001353
Reference score
- Variants: 6
- Variants ignored: 1
-
Trait: Parkinson's disease
- Mapped Trait(s):
- Samples: 31,575
- Population:
- Publication: Sia MW et.al, Mov Disord (2021-08-17)
- View in PGS-Catalog
Target study
- Coverage: 5 (83.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001354
Reference score
- Variants: 12
- Variants ignored: 4
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Samples: 290,551
- Population:
- Publication: Song N et.al, Cancer Epidemiol Biomarkers Prev (2021-08-31)
- View in PGS-Catalog
Target study
- Coverage: 8 (66.67%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001355
Reference score
- Variants: 2,994,055
- Variants ignored: 0
-
Trait: Coronary artery disease
- Mapped Trait(s):
- Samples: 184,305
- Population:
- Publication: Ye Y et.al, Circ Genom Precis Med (2021-01-12)
- View in PGS-Catalog
Target study
- Coverage: 2,994,055 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001356
Reference score
- Variants: 2,996,793
- Variants ignored: 0
-
Trait: Atrial fibrillation
- Mapped Trait(s):
- Samples: 133,073
- Population:
- Publication: Ye Y et.al, Circ Genom Precis Med (2021-01-12)
- View in PGS-Catalog
Target study
- Coverage: 2,996,793 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001357
Reference score
- Variants: 2,996,761
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 159,208
- Population:
- Publication: Ye Y et.al, Circ Genom Precis Med (2021-01-12)
- View in PGS-Catalog
Target study
- Coverage: 2,996,761 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001358
Reference score
- Variants: 148
- Variants ignored: 0
-
Trait: 3mm cylindrical power (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 132 (89.19%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001359
Reference score
- Variants: 9,497
- Variants ignored: 0
-
Trait: 3mm strong meridian (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 9,010 (94.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001360
Reference score
- Variants: 10,082
- Variants ignored: 9
-
Trait: 3mm strong meridian (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 9,566 (94.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001361
Reference score
- Variants: 976
- Variants ignored: 0
-
Trait: 3mm strong meridian angle (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 880 (90.16%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001362
Reference score
- Variants: 8,600
- Variants ignored: 9
-
Trait: 3mm weak meridian (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 8,175 (95.06%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001363
Reference score
- Variants: 8,983
- Variants ignored: 9
-
Trait: 3mm weak meridian (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 8,522 (94.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001364
Reference score
- Variants: 319
- Variants ignored: 0
-
Trait: 6mm cylindrical power angle (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 287 (89.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001365
Reference score
- Variants: 8,504
- Variants ignored: 9
-
Trait: 6mm strong meridian (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 8,072 (94.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001366
Reference score
- Variants: 9,219
- Variants ignored: 9
-
Trait: 6mm strong meridian (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 8,726 (94.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001367
Reference score
- Variants: 8,580
- Variants ignored: 0
-
Trait: 6mm weak meridian (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 8,136 (94.83%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001368
Reference score
- Variants: 8,730
- Variants ignored: 0
-
Trait: 6mm weak meridian (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 8,274 (94.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001369
Reference score
- Variants: 4
- Variants ignored: 0
-
Trait: Acute appendicitis (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3 (75%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001370
Reference score
- Variants: 922
- Variants ignored: 18
-
Trait: Age asthma diagnosed
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 831 (90.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001371
Reference score
- Variants: 26
- Variants ignored: 18
-
Trait: Age diabetes diagnosed
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 19 (73.08%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001372
Reference score
- Variants: 255
- Variants ignored: 9
-
Trait: Age hayfever or allergic rhinitis diagnosed by doctor
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 236 (92.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001373
Reference score
- Variants: 8,870
- Variants ignored: 0
-
Trait: Age started wearing glasses or contact lenses
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 8,382 (94.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001374
Reference score
- Variants: 663
- Variants ignored: 0
-
Trait: Age stopped smoking
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 571 (86.12%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001375
Reference score
- Variants: 243
- Variants ignored: 0
-
Trait: Average heart rate
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 217 (89.3%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001376
Reference score
- Variants: 845
- Variants ignored: 0
-
Trait: Average number of times bowels opened per day
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 762 (90.18%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001377
Reference score
- Variants: 3,205
- Variants ignored: 0
-
Trait: Basophill %
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3,012 (93.98%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001378
Reference score
- Variants: 3,050
- Variants ignored: 0
-
Trait: Basophill count
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,871 (94.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001379
Reference score
- Variants: 850
- Variants ignored: 0
-
Trait: Body surface area
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 781 (91.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001380
Reference score
- Variants: 2,240
- Variants ignored: 0
-
Trait: Corneal hysteresis (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,087 (93.17%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001381
Reference score
- Variants: 2,500
- Variants ignored: 18
-
Trait: Corneal hysteresis (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,323 (92.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001382
Reference score
- Variants: 2,390
- Variants ignored: 0
-
Trait: Corneal resistance factor (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,222 (92.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001383
Reference score
- Variants: 3,941
- Variants ignored: 0
-
Trait: Corneal resistance factor (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3,686 (93.53%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001384
Reference score
- Variants: 1,526
- Variants ignored: 9
-
Trait: Degree bothered by feeling tired all the time in the last 3 months
- Mapped Trait(s):
- EFO_0011014: health-related quality of life measurement
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,410 (92.4%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001385
Reference score
- Variants: 9
- Variants ignored: 0
-
Trait: Degree bothered by headaches in the last 3 months
- Mapped Trait(s):
- EFO_0011014: health-related quality of life measurement
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 9 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001386
Reference score
- Variants: 534
- Variants ignored: 0
-
Trait: Degree bothered by pain in arms/legs/joints in the past 3 months
- Mapped Trait(s):
- EFO_0011014: health-related quality of life measurement
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 486 (91.01%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001387
Reference score
- Variants: 333
- Variants ignored: 0
-
Trait: Degree bothered by urinary frequency/bladder irritability in the last 3 months
- Mapped Trait(s):
- EFO_0011014: health-related quality of life measurement
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 297 (89.19%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001388
Reference score
- Variants: 1
- Variants ignored: 0
-
Trait: Difficulty not smoking for 1 day
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001389
Reference score
- Variants: 989
- Variants ignored: 0
-
Trait: Dried fruit intake
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 886 (89.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001390
Reference score
- Variants: 220
- Variants ignored: 0
-
Trait: Duodenal ulcer (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 180 (81.82%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001391
Reference score
- Variants: 819
- Variants ignored: 9
-
Trait: Ever taken cannabis
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 722 (88.16%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001392
Reference score
- Variants: 312
- Variants ignored: 0
-
Trait: Family history of lung cancer
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 277 (88.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001393
Reference score
- Variants: 398
- Variants ignored: 0
-
Trait: Father's age at death
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 350 (87.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001394
Reference score
- Variants: 860
- Variants ignored: 0
-
Trait: Freq. of drinking alcohol
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 783 (91.05%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001395
Reference score
- Variants: 256
- Variants ignored: 9
-
Trait: Frequency of discomfort/pain in abdomen in last 3 months
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 230 (89.84%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001396
Reference score
- Variants: 2,431
- Variants ignored: 18
-
Trait: Frequency of unenthusiasm / disinterest in last 2 weeks
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,235 (91.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001397
Reference score
- Variants: 1,276
- Variants ignored: 0
-
Trait: Frequency of walking for pleasure in last 4 weeks
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,158 (90.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001398
Reference score
- Variants: 659
- Variants ignored: 0
-
Trait: Friendship satisfaction
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 597 (90.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001399
Reference score
- Variants: 5
- Variants ignored: 0
-
Trait: GE / gI antigen for Varicella Zoster Virus
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3 (60%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001400
Reference score
- Variants: 15,602
- Variants ignored: 18
-
Trait: Haemoglobin concentration
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 14,771 (94.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001401
Reference score
- Variants: 1,814
- Variants ignored: 9
-
Trait: Health satisfaction
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,681 (92.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001402
Reference score
- Variants: 14,251
- Variants ignored: 18
-
Trait: Heel bone mineral density (BMD)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 13,499 (94.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001403
Reference score
- Variants: 8,285
- Variants ignored: 9
-
Trait: Heel bone mineral density (BMD) (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 7,774 (93.83%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001404
Reference score
- Variants: 9,637
- Variants ignored: 0
-
Trait: Heel bone mineral density (BMD) (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 9,074 (94.16%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001405
Reference score
- Variants: 3,166
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,935 (92.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001406
Reference score
- Variants: 15,856
- Variants ignored: 18
-
Trait: High light scatter reticulocyte count
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 15,027 (94.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001407
Reference score
- Variants: 66
- Variants ignored: 27
-
Trait: HTLV-1 gag antigen for Human T-Lymphotropic Virus 1
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 47 (71.21%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001408
Reference score
- Variants: 10,871
- Variants ignored: 9
-
Trait: Immature reticulocyte fraction
- Mapped Trait(s):
- EFO_0009253: Immature Reticulocyte Fraction Measurement
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 10,290 (94.66%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001409
Reference score
- Variants: 1,166
- Variants ignored: 0
-
Trait: Intra-ocular pressure, corneal-compensated (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,061 (90.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001410
Reference score
- Variants: 1,563
- Variants ignored: 9
-
Trait: Intra-ocular pressure, corneal-compensated (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,419 (90.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001411
Reference score
- Variants: 3,513
- Variants ignored: 0
-
Trait: Intra-ocular pressure, Goldmann-correlated (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3,261 (92.83%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001412
Reference score
- Variants: 266
- Variants ignored: 9
-
Trait: LV ejection fraction
- Mapped Trait(s):
- EFO_0008373: left ventricular ejection fraction measurement
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 229 (86.09%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001413
Reference score
- Variants: 26
- Variants ignored: 0
-
Trait: LV stroke volume
- Mapped Trait(s):
- EFO_0010555: left ventricular stroke volume measurement
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 23 (88.46%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001414
Reference score
- Variants: 15,143
- Variants ignored: 54
-
Trait: Lymphocyte %
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 14,427 (95.27%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001415
Reference score
- Variants: 731
- Variants ignored: 0
-
Trait: Mean FA in anterior limb of internal capsule on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 661 (90.42%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001416
Reference score
- Variants: 1,280
- Variants ignored: 0
-
Trait: Mean FA in anterior limb of internal capsule on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,172 (91.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001417
Reference score
- Variants: 754
- Variants ignored: 0
-
Trait: Mean FA in body of corpus callosum on FA skeleton
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 689 (91.38%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001418
Reference score
- Variants: 1,295
- Variants ignored: 0
-
Trait: Mean FA in cerebral peduncle on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,185 (91.51%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001419
Reference score
- Variants: 895
- Variants ignored: 0
-
Trait: Mean FA in cingulum cingulate gyrus on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 815 (91.06%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001420
Reference score
- Variants: 1,224
- Variants ignored: 9
-
Trait: Mean FA in cingulum cingulate gyrus on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,097 (89.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001421
Reference score
- Variants: 330
- Variants ignored: 0
-
Trait: Mean FA in cingulum hippocampus on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 294 (89.09%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001422
Reference score
- Variants: 879
- Variants ignored: 0
-
Trait: Mean FA in cingulum hippocampus on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 799 (90.9%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001423
Reference score
- Variants: 342
- Variants ignored: 0
-
Trait: Mean FA in corticospinal tract on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 304 (88.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001424
Reference score
- Variants: 940
- Variants ignored: 0
-
Trait: Mean FA in external capsule on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 849 (90.32%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001425
Reference score
- Variants: 1,174
- Variants ignored: 0
-
Trait: Mean FA in fornix cres+stria terminalis on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,046 (89.1%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001426
Reference score
- Variants: 836
- Variants ignored: 9
-
Trait: Mean FA in fornix on FA skeleton
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 735 (87.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001427
Reference score
- Variants: 1,073
- Variants ignored: 0
-
Trait: Mean FA in genu of corpus callosum on FA skeleton
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 967 (90.12%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001428
Reference score
- Variants: 946
- Variants ignored: 0
-
Trait: Mean FA in inferior cerebellar peduncle on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 846 (89.43%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001429
Reference score
- Variants: 1,140
- Variants ignored: 0
-
Trait: Mean FA in middle cerebellar peduncle on FA skeleton
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,047 (91.84%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001430
Reference score
- Variants: 1,796
- Variants ignored: 0
-
Trait: Mean FA in posterior limb of internal capsule on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,656 (92.2%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001431
Reference score
- Variants: 2,080
- Variants ignored: 0
-
Trait: Mean FA in posterior limb of internal capsule on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,932 (92.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001432
Reference score
- Variants: 1,654
- Variants ignored: 0
-
Trait: Mean FA in posterior thalamic radiation on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,522 (92.02%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001433
Reference score
- Variants: 1,877
- Variants ignored: 18
-
Trait: Mean FA in posterior thalamic radiation on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,714 (91.32%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001434
Reference score
- Variants: 1,164
- Variants ignored: 0
-
Trait: Mean FA in retrolenticular part of internal capsule on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,078 (92.61%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001435
Reference score
- Variants: 456
- Variants ignored: 0
-
Trait: Mean FA in retrolenticular part of internal capsule on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 415 (91.01%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001436
Reference score
- Variants: 1,376
- Variants ignored: 9
-
Trait: Mean FA in sagittal stratum on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,247 (90.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001437
Reference score
- Variants: 1,445
- Variants ignored: 0
-
Trait: Mean FA in sagittal stratum on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,325 (91.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001438
Reference score
- Variants: 598
- Variants ignored: 9
-
Trait: Mean FA in splenium of corpus callosum on FA skeleton
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 535 (89.46%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001439
Reference score
- Variants: 1,647
- Variants ignored: 0
-
Trait: Mean FA in superior cerebellar peduncle on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,508 (91.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001440
Reference score
- Variants: 1,860
- Variants ignored: 0
-
Trait: Mean FA in superior cerebellar peduncle on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,709 (91.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001441
Reference score
- Variants: 821
- Variants ignored: 0
-
Trait: Mean FA in superior corona radiata on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 749 (91.23%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001442
Reference score
- Variants: 1,238
- Variants ignored: 0
-
Trait: Mean FA in superior corona radiata on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,143 (92.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001443
Reference score
- Variants: 1,286
- Variants ignored: 0
-
Trait: Mean FA in superior fronto-occipital fasciculus on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,180 (91.76%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001444
Reference score
- Variants: 480
- Variants ignored: 0
-
Trait: Mean FA in superior fronto-occipital fasciculus on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 426 (88.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001445
Reference score
- Variants: 3,389
- Variants ignored: 9
-
Trait: Mean FA in superior longitudinal fasciculus on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3,134 (92.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001446
Reference score
- Variants: 1,463
- Variants ignored: 0
-
Trait: Mean FA in superior longitudinal fasciculus on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,347 (92.07%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001447
Reference score
- Variants: 1,202
- Variants ignored: 0
-
Trait: Mean FA in tapetum on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,108 (92.18%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001448
Reference score
- Variants: 1,948
- Variants ignored: 9
-
Trait: Mean FA in tapetum on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,768 (90.76%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001449
Reference score
- Variants: 727
- Variants ignored: 0
-
Trait: Mean FA in uncinate fasciculus on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 670 (92.16%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001450
Reference score
- Variants: 1,490
- Variants ignored: 0
-
Trait: Mean ICVF in anterior corona radiata on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,381 (92.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001451
Reference score
- Variants: 2,090
- Variants ignored: 9
-
Trait: Mean ICVF in anterior corona radiata on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,931 (92.39%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001452
Reference score
- Variants: 870
- Variants ignored: 0
-
Trait: Mean ICVF in anterior limb of internal capsule on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 793 (91.15%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001453
Reference score
- Variants: 1,308
- Variants ignored: 0
-
Trait: Mean ICVF in anterior limb of internal capsule on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,210 (92.51%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001454
Reference score
- Variants: 2,881
- Variants ignored: 9
-
Trait: Mean ICVF in body of corpus callosum on FA skeleton
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,670 (92.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001455
Reference score
- Variants: 1,907
- Variants ignored: 0
-
Trait: Mean ICVF in cerebral peduncle on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,763 (92.45%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001456
Reference score
- Variants: 1,501
- Variants ignored: 0
-
Trait: Mean ICVF in cerebral peduncle on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,365 (90.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001457
Reference score
- Variants: 1,929
- Variants ignored: 9
-
Trait: Mean ICVF in cingulum cingulate gyrus on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,786 (92.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001458
Reference score
- Variants: 3,061
- Variants ignored: 9
-
Trait: Mean ICVF in cingulum cingulate gyrus on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,827 (92.36%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001459
Reference score
- Variants: 1,153
- Variants ignored: 9
-
Trait: Mean ICVF in cingulum hippocampus on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,045 (90.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001460
Reference score
- Variants: 2,400
- Variants ignored: 9
-
Trait: Mean ICVF in cingulum hippocampus on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,195 (91.46%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001461
Reference score
- Variants: 724
- Variants ignored: 0
-
Trait: Mean ICVF in external capsule on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 650 (89.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001462
Reference score
- Variants: 1,316
- Variants ignored: 0
-
Trait: Mean ICVF in external capsule on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,202 (91.34%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001463
Reference score
- Variants: 1,353
- Variants ignored: 0
-
Trait: Mean ICVF in fornix cres+stria terminalis on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,244 (91.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001464
Reference score
- Variants: 2,387
- Variants ignored: 0
-
Trait: Mean ICVF in fornix cres+stria terminalis on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,217 (92.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001465
Reference score
- Variants: 188
- Variants ignored: 0
-
Trait: Mean ICVF in fornix on FA skeleton
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 169 (89.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001466
Reference score
- Variants: 2,530
- Variants ignored: 9
-
Trait: Mean ICVF in genu of corpus callosum on FA skeleton
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,349 (92.85%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001467
Reference score
- Variants: 711
- Variants ignored: 0
-
Trait: Mean ICVF in inferior cerebellar peduncle on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 640 (90.01%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001468
Reference score
- Variants: 1,262
- Variants ignored: 0
-
Trait: Mean ICVF in inferior cerebellar peduncle on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,160 (91.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001469
Reference score
- Variants: 246
- Variants ignored: 0
-
Trait: Mean ICVF in medial lemniscus on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 214 (86.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001470
Reference score
- Variants: 250
- Variants ignored: 0
-
Trait: Mean ICVF in medial lemniscus on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 224 (89.6%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001471
Reference score
- Variants: 1,580
- Variants ignored: 9
-
Trait: Mean ICVF in middle cerebellar peduncle on FA skeleton
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,433 (90.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001472
Reference score
- Variants: 2,727
- Variants ignored: 9
-
Trait: Mean ICVF in posterior corona radiata on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,535 (92.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001473
Reference score
- Variants: 1,934
- Variants ignored: 0
-
Trait: Mean ICVF in posterior corona radiata on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,786 (92.35%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001474
Reference score
- Variants: 2,010
- Variants ignored: 9
-
Trait: Mean ICVF in posterior limb of internal capsule on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,863 (92.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001475
Reference score
- Variants: 1,957
- Variants ignored: 9
-
Trait: Mean ICVF in posterior limb of internal capsule on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,794 (91.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001476
Reference score
- Variants: 2,073
- Variants ignored: 9
-
Trait: Mean ICVF in posterior thalamic radiation on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,933 (93.25%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001477
Reference score
- Variants: 1,753
- Variants ignored: 9
-
Trait: Mean ICVF in posterior thalamic radiation on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,627 (92.81%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001478
Reference score
- Variants: 2,268
- Variants ignored: 9
-
Trait: Mean ICVF in retrolenticular part of internal capsule on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,099 (92.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001479
Reference score
- Variants: 2,113
- Variants ignored: 9
-
Trait: Mean ICVF in retrolenticular part of internal capsule on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,952 (92.38%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001480
Reference score
- Variants: 1,651
- Variants ignored: 9
-
Trait: Mean ICVF in sagittal stratum on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,518 (91.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001481
Reference score
- Variants: 2,195
- Variants ignored: 9
-
Trait: Mean ICVF in sagittal stratum on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,029 (92.44%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001482
Reference score
- Variants: 2,068
- Variants ignored: 0
-
Trait: Mean ICVF in superior cerebellar peduncle on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,891 (91.44%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001483
Reference score
- Variants: 1,420
- Variants ignored: 0
-
Trait: Mean ICVF in superior cerebellar peduncle on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,291 (90.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001484
Reference score
- Variants: 2,789
- Variants ignored: 0
-
Trait: Mean ICVF in superior corona radiata on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,576 (92.36%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001485
Reference score
- Variants: 2,299
- Variants ignored: 0
-
Trait: Mean ICVF in superior corona radiata on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,128 (92.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001486
Reference score
- Variants: 402
- Variants ignored: 0
-
Trait: Mean ICVF in superior fronto-occipital fasciculus on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 357 (88.81%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001487
Reference score
- Variants: 703
- Variants ignored: 0
-
Trait: Mean ICVF in superior fronto-occipital fasciculus on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 630 (89.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001488
Reference score
- Variants: 1,974
- Variants ignored: 9
-
Trait: Mean ICVF in superior longitudinal fasciculus on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,827 (92.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001489
Reference score
- Variants: 1,750
- Variants ignored: 9
-
Trait: Mean ICVF in superior longitudinal fasciculus on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,625 (92.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001490
Reference score
- Variants: 1,117
- Variants ignored: 0
-
Trait: Mean ICVF in tapetum on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,014 (90.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001491
Reference score
- Variants: 962
- Variants ignored: 0
-
Trait: Mean ICVF in uncinate fasciculus on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 870 (90.44%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001492
Reference score
- Variants: 641
- Variants ignored: 0
-
Trait: Mean ICVF in uncinate fasciculus on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 573 (89.39%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001493
Reference score
- Variants: 393
- Variants ignored: 9
-
Trait: Mean ISOVF in anterior corona radiata on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 344 (87.53%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001494
Reference score
- Variants: 116
- Variants ignored: 9
-
Trait: Mean ISOVF in anterior corona radiata on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 99 (85.34%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001495
Reference score
- Variants: 627
- Variants ignored: 0
-
Trait: Mean ISOVF in body of corpus callosum on FA skeleton
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 566 (90.27%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001496
Reference score
- Variants: 114
- Variants ignored: 9
-
Trait: Mean ISOVF in cingulum cingulate gyrus on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 92 (80.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001497
Reference score
- Variants: 157
- Variants ignored: 9
-
Trait: Mean ISOVF in cingulum cingulate gyrus on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 134 (85.35%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001498
Reference score
- Variants: 142
- Variants ignored: 9
-
Trait: Mean ISOVF in external capsule on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 120 (84.51%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001499
Reference score
- Variants: 733
- Variants ignored: 9
-
Trait: Mean ISOVF in fornix on FA skeleton
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 657 (89.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001500
Reference score
- Variants: 466
- Variants ignored: 9
-
Trait: Mean ISOVF in posterior corona radiata on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 414 (88.84%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001501
Reference score
- Variants: 554
- Variants ignored: 0
-
Trait: Mean ISOVF in posterior thalamic radiation on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 491 (88.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001502
Reference score
- Variants: 400
- Variants ignored: 9
-
Trait: Mean ISOVF in sagittal stratum on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 337 (84.25%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001503
Reference score
- Variants: 709
- Variants ignored: 9
-
Trait: Mean ISOVF in sagittal stratum on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 630 (88.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001504
Reference score
- Variants: 666
- Variants ignored: 0
-
Trait: Mean ISOVF in superior cerebellar peduncle on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 595 (89.34%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001505
Reference score
- Variants: 257
- Variants ignored: 9
-
Trait: Mean ISOVF in superior corona radiata on FA skeleton (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 224 (87.16%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001506
Reference score
- Variants: 392
- Variants ignored: 9
-
Trait: Mean ISOVF in superior corona radiata on FA skeleton (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 356 (90.82%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001507
Reference score
- Variants: 1,009
- Variants ignored: 0
-
Trait: Median T2star in caudate (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 912 (90.39%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001508
Reference score
- Variants: 930
- Variants ignored: 9
-
Trait: Median T2star in caudate (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 850 (91.4%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001509
Reference score
- Variants: 942
- Variants ignored: 9
-
Trait: Median T2star in pallidum (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 850 (90.23%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001510
Reference score
- Variants: 2,164
- Variants ignored: 0
-
Trait: Median T2star in pallidum (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,985 (91.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001511
Reference score
- Variants: 1,922
- Variants ignored: 0
-
Trait: Median T2star in putamen (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,775 (92.35%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001512
Reference score
- Variants: 2,474
- Variants ignored: 9
-
Trait: Median T2star in putamen (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,305 (93.17%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001513
Reference score
- Variants: 114
- Variants ignored: 0
-
Trait: Median T2star in thalamus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 99 (86.84%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001514
Reference score
- Variants: 273
- Variants ignored: 18
-
Trait: Non-cancer illness year/age first occurred
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 247 (90.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001515
Reference score
- Variants: 9
- Variants ignored: 0
-
Trait: Number of cigarettes currently smoked daily (current cigarette smokers)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 7 (77.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001516
Reference score
- Variants: 90
- Variants ignored: 0
-
Trait: Other diseases of intestine (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 73 (81.11%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001517
Reference score
- Variants: 20,910
- Variants ignored: 36
-
Trait: Platelet crit
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 19,973 (95.52%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001518
Reference score
- Variants: 591
- Variants ignored: 0
-
Trait: Portion size
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 532 (90.02%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001519
Reference score
- Variants: 693
- Variants ignored: 0
-
Trait: Position of pulse wave notch
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 625 (90.19%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001520
Reference score
- Variants: 1,358
- Variants ignored: 0
-
Trait: Position of the pulse wave peak
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,249 (91.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001521
Reference score
- Variants: 391
- Variants ignored: 0
-
Trait: PQ interval
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 339 (86.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001522
Reference score
- Variants: 17
- Variants ignored: 0
-
Trait: Psoriatic and enteropathic arthropathies (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 13 (76.47%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001523
Reference score
- Variants: 4,117
- Variants ignored: 0
-
Trait: Pulse rate
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 3,803 (92.37%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001524
Reference score
- Variants: 765
- Variants ignored: 0
-
Trait: Pulse rate (during blood-pressure measurement)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 694 (90.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001525
Reference score
- Variants: 401
- Variants ignored: 0
-
Trait: QRS duration
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 338 (84.29%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001526
Reference score
- Variants: 609
- Variants ignored: 0
-
Trait: QT interval
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 532 (87.36%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001527
Reference score
- Variants: 115
- Variants ignored: 0
-
Trait: QTC interval (QT interval according to Bazett)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 101 (87.83%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001528
Reference score
- Variants: 6,262
- Variants ignored: 9
-
Trait: Reticulocyte count
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 5,851 (93.44%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001529
Reference score
- Variants: 13,172
- Variants ignored: 0
-
Trait: Speed of sound through heel
- Mapped Trait(s):
- EFO_0007772: calcaneal bone quantitative ultrasound measurement
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 12,476 (94.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001530
Reference score
- Variants: 8,419
- Variants ignored: 9
-
Trait: Speed of sound through heel (L)
- Mapped Trait(s):
- EFO_0007772: calcaneal bone quantitative ultrasound measurement
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 7,870 (93.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001531
Reference score
- Variants: 8,912
- Variants ignored: 0
-
Trait: Speed of sound through heel (R)
- Mapped Trait(s):
- EFO_0007772: calcaneal bone quantitative ultrasound measurement
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 8,398 (94.23%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001532
Reference score
- Variants: 86
- Variants ignored: 0
-
Trait: Time from waking to first cigarette
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 74 (86.05%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001533
Reference score
- Variants: 343
- Variants ignored: 0
-
Trait: Tinnitus severity
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 305 (88.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001534
Reference score
- Variants: 355
- Variants ignored: 0
-
Trait: Total Volume of white matter hyperintensities (from T1 and T2 FLAIR images)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 318 (89.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001535
Reference score
- Variants: 309
- Variants ignored: 0
-
Trait: Use of sun/uv protection (Sometimes)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 273 (88.35%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001536
Reference score
- Variants: 77
- Variants ignored: 18
-
Trait: Vitiligo (time-to-event)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 64 (83.12%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001537
Reference score
- Variants: 647
- Variants ignored: 0
-
Trait: Volume of accumbens (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 564 (87.17%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001538
Reference score
- Variants: 643
- Variants ignored: 0
-
Trait: Volume of accumbens (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 577 (89.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001539
Reference score
- Variants: 1,183
- Variants ignored: 0
-
Trait: Volume of brain stem + 4th ventricle
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,078 (91.12%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001540
Reference score
- Variants: 1,871
- Variants ignored: 0
-
Trait: Volume of brain, grey+white matter
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,717 (91.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001541
Reference score
- Variants: 1,999
- Variants ignored: 18
-
Trait: Volume of brain, grey+white matter (normalised for head size)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,859 (93%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001542
Reference score
- Variants: 1,055
- Variants ignored: 0
-
Trait: Volume of caudate (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 959 (90.9%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001543
Reference score
- Variants: 1,910
- Variants ignored: 0
-
Trait: Volume of caudate (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,755 (91.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001544
Reference score
- Variants: 2,061
- Variants ignored: 0
-
Trait: Volume of grey matter
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,896 (91.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001545
Reference score
- Variants: 1,139
- Variants ignored: 0
-
Trait: Volume of grey matter (normalised for head size)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,045 (91.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001546
Reference score
- Variants: 115
- Variants ignored: 0
-
Trait: Volume of grey matter in Amygdala (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 93 (80.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001547
Reference score
- Variants: 632
- Variants ignored: 0
-
Trait: Volume of grey matter in Brain-Stem
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 569 (90.03%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001548
Reference score
- Variants: 194
- Variants ignored: 0
-
Trait: Volume of grey matter in Central Opercular Cortex (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 170 (87.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001549
Reference score
- Variants: 1,123
- Variants ignored: 0
-
Trait: Volume of grey matter in Central Opercular Cortex (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,004 (89.4%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001550
Reference score
- Variants: 389
- Variants ignored: 0
-
Trait: Volume of grey matter in Cingulate Gyrus, anterior division (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 338 (86.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001551
Reference score
- Variants: 244
- Variants ignored: 0
-
Trait: Volume of grey matter in Cingulate Gyrus, anterior division (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 201 (82.38%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001552
Reference score
- Variants: 652
- Variants ignored: 0
-
Trait: Volume of grey matter in Cingulate Gyrus, posterior division (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 573 (87.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001553
Reference score
- Variants: 2,371
- Variants ignored: 9
-
Trait: Volume of grey matter in Crus I Cerebellum (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,170 (91.52%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001554
Reference score
- Variants: 1,913
- Variants ignored: 0
-
Trait: Volume of grey matter in Crus II Cerebellum (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,762 (92.11%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001555
Reference score
- Variants: 2,510
- Variants ignored: 0
-
Trait: Volume of grey matter in Crus II Cerebellum (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,340 (93.23%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001556
Reference score
- Variants: 930
- Variants ignored: 9
-
Trait: Volume of grey matter in Cuneal Cortex (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 844 (90.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001557
Reference score
- Variants: 804
- Variants ignored: 9
-
Trait: Volume of grey matter in Frontal Operculum Cortex (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 720 (89.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001558
Reference score
- Variants: 826
- Variants ignored: 9
-
Trait: Volume of grey matter in Frontal Orbital Cortex (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 742 (89.83%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001559
Reference score
- Variants: 592
- Variants ignored: 0
-
Trait: Volume of grey matter in Frontal Orbital Cortex (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 526 (88.85%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001560
Reference score
- Variants: 2,320
- Variants ignored: 0
-
Trait: Volume of grey matter in Frontal Pole (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,127 (91.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001561
Reference score
- Variants: 1,604
- Variants ignored: 0
-
Trait: Volume of grey matter in Heschl's Gyrus (includes H1 and H2) (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,465 (91.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001562
Reference score
- Variants: 1,524
- Variants ignored: 0
-
Trait: Volume of grey matter in Heschl's Gyrus (includes H1 and H2) (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,390 (91.21%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001563
Reference score
- Variants: 1,427
- Variants ignored: 0
-
Trait: Volume of grey matter in Hippocampus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,305 (91.45%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001564
Reference score
- Variants: 1,336
- Variants ignored: 0
-
Trait: Volume of grey matter in Hippocampus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,231 (92.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001565
Reference score
- Variants: 775
- Variants ignored: 0
-
Trait: Volume of grey matter in I-IV Cerebellum (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 693 (89.42%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001566
Reference score
- Variants: 612
- Variants ignored: 0
-
Trait: Volume of grey matter in I-IV Cerebellum (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 548 (89.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001567
Reference score
- Variants: 697
- Variants ignored: 0
-
Trait: Volume of grey matter in Inferior Frontal Gyrus, pars triangularis (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 626 (89.81%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001568
Reference score
- Variants: 288
- Variants ignored: 0
-
Trait: Volume of grey matter in Inferior Temporal Gyrus, posterior division (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 262 (90.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001569
Reference score
- Variants: 1,554
- Variants ignored: 0
-
Trait: Volume of grey matter in Insular Cortex (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,418 (91.25%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001570
Reference score
- Variants: 1,365
- Variants ignored: 0
-
Trait: Volume of grey matter in Insular Cortex (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,251 (91.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001571
Reference score
- Variants: 2,025
- Variants ignored: 9
-
Trait: Volume of grey matter in Intracalcarine Cortex (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,879 (92.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001572
Reference score
- Variants: 1,245
- Variants ignored: 0
-
Trait: Volume of grey matter in IX Cerebellum (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,118 (89.8%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001573
Reference score
- Variants: 1,972
- Variants ignored: 0
-
Trait: Volume of grey matter in IX Cerebellum (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,804 (91.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001574
Reference score
- Variants: 1,159
- Variants ignored: 0
-
Trait: Volume of grey matter in Lateral Occipital Cortex, inferior division (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,052 (90.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001575
Reference score
- Variants: 581
- Variants ignored: 0
-
Trait: Volume of grey matter in Lateral Occipital Cortex, superior division (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 522 (89.85%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001576
Reference score
- Variants: 781
- Variants ignored: 0
-
Trait: Volume of grey matter in Lingual Gyrus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 704 (90.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001577
Reference score
- Variants: 369
- Variants ignored: 0
-
Trait: Volume of grey matter in Middle Frontal Gyrus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 333 (90.24%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001578
Reference score
- Variants: 489
- Variants ignored: 0
-
Trait: Volume of grey matter in Middle Frontal Gyrus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 435 (88.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001579
Reference score
- Variants: 1,076
- Variants ignored: 0
-
Trait: Volume of grey matter in Middle Temporal Gyrus, posterior division (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 971 (90.24%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001580
Reference score
- Variants: 235
- Variants ignored: 0
-
Trait: Volume of grey matter in Occipital Fusiform Gyrus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 206 (87.66%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001581
Reference score
- Variants: 1,616
- Variants ignored: 0
-
Trait: Volume of grey matter in Occipital Pole (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,462 (90.47%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001582
Reference score
- Variants: 145
- Variants ignored: 0
-
Trait: Volume of grey matter in Paracingulate Gyrus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 131 (90.34%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001583
Reference score
- Variants: 1,724
- Variants ignored: 0
-
Trait: Volume of grey matter in Parahippocampal Gyrus, anterior division (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,568 (90.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001584
Reference score
- Variants: 1,250
- Variants ignored: 0
-
Trait: Volume of grey matter in Parahippocampal Gyrus, anterior division (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,130 (90.4%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001585
Reference score
- Variants: 1,120
- Variants ignored: 0
-
Trait: Volume of grey matter in Parahippocampal Gyrus, posterior division (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,032 (92.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001586
Reference score
- Variants: 1,078
- Variants ignored: 0
-
Trait: Volume of grey matter in Parahippocampal Gyrus, posterior division (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 985 (91.37%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001587
Reference score
- Variants: 1,316
- Variants ignored: 0
-
Trait: Volume of grey matter in Planum Polare (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,206 (91.64%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001588
Reference score
- Variants: 989
- Variants ignored: 0
-
Trait: Volume of grey matter in Planum Polare (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 917 (92.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001589
Reference score
- Variants: 2,019
- Variants ignored: 9
-
Trait: Volume of grey matter in Planum Temporale (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,842 (91.23%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001590
Reference score
- Variants: 318
- Variants ignored: 0
-
Trait: Volume of grey matter in Precentral Gyrus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 287 (90.25%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001591
Reference score
- Variants: 1,370
- Variants ignored: 0
-
Trait: Volume of grey matter in Precentral Gyrus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,251 (91.31%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001592
Reference score
- Variants: 2,184
- Variants ignored: 0
-
Trait: Volume of grey matter in Precuneous Cortex (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,998 (91.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001593
Reference score
- Variants: 274
- Variants ignored: 0
-
Trait: Volume of grey matter in Putamen (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 238 (86.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001594
Reference score
- Variants: 562
- Variants ignored: 0
-
Trait: Volume of grey matter in Putamen (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 495 (88.08%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001595
Reference score
- Variants: 1,978
- Variants ignored: 0
-
Trait: Volume of grey matter in Subcallosal Cortex (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,813 (91.66%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001596
Reference score
- Variants: 1,458
- Variants ignored: 0
-
Trait: Volume of grey matter in Subcallosal Cortex (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,335 (91.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001597
Reference score
- Variants: 1,049
- Variants ignored: 0
-
Trait: Volume of grey matter in Superior Frontal Gyrus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 952 (90.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001598
Reference score
- Variants: 5
- Variants ignored: 0
-
Trait: Volume of grey matter in Superior Frontal Gyrus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 4 (80%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001599
Reference score
- Variants: 728
- Variants ignored: 0
-
Trait: Volume of grey matter in Superior Temporal Gyrus, anterior division (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 646 (88.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001600
Reference score
- Variants: 530
- Variants ignored: 0
-
Trait: Volume of grey matter in Superior Temporal Gyrus, posterior division (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 469 (88.49%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001601
Reference score
- Variants: 446
- Variants ignored: 0
-
Trait: Volume of grey matter in Supracalcarine Cortex (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 403 (90.36%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001602
Reference score
- Variants: 527
- Variants ignored: 0
-
Trait: Volume of grey matter in Supracalcarine Cortex (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 484 (91.84%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001603
Reference score
- Variants: 264
- Variants ignored: 0
-
Trait: Volume of grey matter in Temporal Fusiform Cortex, anterior division (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 240 (90.91%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001604
Reference score
- Variants: 1,533
- Variants ignored: 0
-
Trait: Volume of grey matter in Temporal Fusiform Cortex, posterior division (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,418 (92.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001605
Reference score
- Variants: 1,447
- Variants ignored: 9
-
Trait: Volume of grey matter in Temporal Fusiform Cortex, posterior division (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,335 (92.26%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001606
Reference score
- Variants: 1,200
- Variants ignored: 0
-
Trait: Volume of grey matter in Temporal Pole (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,082 (90.17%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001607
Reference score
- Variants: 1,025
- Variants ignored: 0
-
Trait: Volume of grey matter in Temporal Pole (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 928 (90.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001608
Reference score
- Variants: 2,508
- Variants ignored: 0
-
Trait: Volume of grey matter in Thalamus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,314 (92.26%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001609
Reference score
- Variants: 885
- Variants ignored: 0
-
Trait: Volume of grey matter in Thalamus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 806 (91.07%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001610
Reference score
- Variants: 1,592
- Variants ignored: 0
-
Trait: Volume of grey matter in V Cerebellum (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,443 (90.64%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001611
Reference score
- Variants: 184
- Variants ignored: 0
-
Trait: Volume of grey matter in V Cerebellum (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 163 (88.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001612
Reference score
- Variants: 687
- Variants ignored: 0
-
Trait: Volume of grey matter in Ventral Striatum (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 614 (89.37%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001613
Reference score
- Variants: 221
- Variants ignored: 0
-
Trait: Volume of grey matter in Ventral Striatum (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 190 (85.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001614
Reference score
- Variants: 837
- Variants ignored: 0
-
Trait: Volume of grey matter in Vermis Crus II Cerebellum
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 764 (91.28%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001615
Reference score
- Variants: 1,369
- Variants ignored: 0
-
Trait: Volume of grey matter in Vermis IX Cerebellum
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,236 (90.28%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001616
Reference score
- Variants: 612
- Variants ignored: 0
-
Trait: Volume of grey matter in Vermis VI Cerebellum
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 546 (89.22%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001617
Reference score
- Variants: 718
- Variants ignored: 0
-
Trait: Volume of grey matter in Vermis VIIb Cerebellum
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 654 (91.09%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001618
Reference score
- Variants: 776
- Variants ignored: 0
-
Trait: Volume of grey matter in Vermis VIIIa Cerebellum
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 698 (89.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001619
Reference score
- Variants: 1,916
- Variants ignored: 0
-
Trait: Volume of grey matter in Vermis VIIIb Cerebellum
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,739 (90.76%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001620
Reference score
- Variants: 636
- Variants ignored: 0
-
Trait: Volume of grey matter in Vermis X Cerebellum
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 560 (88.05%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001621
Reference score
- Variants: 902
- Variants ignored: 0
-
Trait: Volume of grey matter in VI Cerebellum (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 808 (89.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001622
Reference score
- Variants: 513
- Variants ignored: 0
-
Trait: Volume of grey matter in VI Cerebellum (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 470 (91.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001623
Reference score
- Variants: 649
- Variants ignored: 0
-
Trait: Volume of grey matter in VIIb Cerebellum (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 588 (90.6%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001624
Reference score
- Variants: 673
- Variants ignored: 0
-
Trait: Volume of grey matter in VIIb Cerebellum (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 607 (90.19%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001625
Reference score
- Variants: 500
- Variants ignored: 0
-
Trait: Volume of grey matter in VIIIa Cerebellum (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 453 (90.6%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001626
Reference score
- Variants: 694
- Variants ignored: 0
-
Trait: Volume of grey matter in VIIIa Cerebellum (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 618 (89.05%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001627
Reference score
- Variants: 819
- Variants ignored: 0
-
Trait: Volume of grey matter in VIIIb Cerebellum (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 730 (89.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001628
Reference score
- Variants: 1,539
- Variants ignored: 0
-
Trait: Volume of grey matter in VIIIb Cerebellum (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,389 (90.25%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001629
Reference score
- Variants: 950
- Variants ignored: 0
-
Trait: Volume of grey matter in X Cerebellum (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 872 (91.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001630
Reference score
- Variants: 442
- Variants ignored: 0
-
Trait: Volume of hippocampus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 394 (89.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001631
Reference score
- Variants: 1,405
- Variants ignored: 9
-
Trait: Volume of pallidum (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,270 (90.39%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001632
Reference score
- Variants: 303
- Variants ignored: 9
-
Trait: Volume of pallidum (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 264 (87.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001633
Reference score
- Variants: 1,920
- Variants ignored: 0
-
Trait: Volume of peripheral cortical grey matter
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,764 (91.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001634
Reference score
- Variants: 1,112
- Variants ignored: 0
-
Trait: Volume of peripheral cortical grey matter (normalised for head size)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,028 (92.45%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001635
Reference score
- Variants: 747
- Variants ignored: 0
-
Trait: Volume of putamen (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 663 (88.76%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001636
Reference score
- Variants: 2,048
- Variants ignored: 9
-
Trait: Volume of putamen (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,881 (91.85%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001637
Reference score
- Variants: 1,328
- Variants ignored: 0
-
Trait: Volume of thalamus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,216 (91.57%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001638
Reference score
- Variants: 1,792
- Variants ignored: 0
-
Trait: Volume of thalamus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,637 (91.35%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001639
Reference score
- Variants: 772
- Variants ignored: 0
-
Trait: Volume of ventricular cerebrospinal fluid
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 685 (88.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001640
Reference score
- Variants: 1,328
- Variants ignored: 9
-
Trait: Volume of white matter
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,197 (90.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001641
Reference score
- Variants: 1,005
- Variants ignored: 9
-
Trait: Volume of white matter (normalised for head size)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 911 (90.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001642
Reference score
- Variants: 1,304
- Variants ignored: 9
-
Trait: Volumetric scaling from T1 head image to standard space
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,205 (92.41%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001643
Reference score
- Variants: 1,025
- Variants ignored: 9
-
Trait: WA FA in tract acoustic radiation (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 935 (91.22%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001644
Reference score
- Variants: 826
- Variants ignored: 0
-
Trait: WA FA in tract acoustic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 756 (91.53%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001645
Reference score
- Variants: 379
- Variants ignored: 0
-
Trait: WA FA in tract anterior thalamic radiation (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 352 (92.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001646
Reference score
- Variants: 726
- Variants ignored: 0
-
Trait: WA FA in tract anterior thalamic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 667 (91.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001647
Reference score
- Variants: 773
- Variants ignored: 0
-
Trait: WA FA in tract cingulate gyrus part of cingulum (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 703 (90.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001648
Reference score
- Variants: 702
- Variants ignored: 0
-
Trait: WA FA in tract cingulate gyrus part of cingulum (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 644 (91.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001649
Reference score
- Variants: 60
- Variants ignored: 0
-
Trait: WA FA in tract corticospinal tract (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 52 (86.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001650
Reference score
- Variants: 1,261
- Variants ignored: 0
-
Trait: WA FA in tract forceps major
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,157 (91.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001651
Reference score
- Variants: 2,017
- Variants ignored: 0
-
Trait: WA FA in tract forceps minor
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,875 (92.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001652
Reference score
- Variants: 597
- Variants ignored: 9
-
Trait: WA FA in tract inferior fronto-occipital fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 537 (89.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001653
Reference score
- Variants: 1,371
- Variants ignored: 0
-
Trait: WA FA in tract inferior fronto-occipital fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,257 (91.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001654
Reference score
- Variants: 709
- Variants ignored: 0
-
Trait: WA FA in tract inferior longitudinal fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 654 (92.24%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001655
Reference score
- Variants: 767
- Variants ignored: 0
-
Trait: WA FA in tract inferior longitudinal fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 694 (90.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001656
Reference score
- Variants: 1,044
- Variants ignored: 0
-
Trait: WA FA in tract posterior thalamic radiation (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 951 (91.09%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001657
Reference score
- Variants: 1,279
- Variants ignored: 9
-
Trait: WA FA in tract posterior thalamic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,165 (91.09%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001658
Reference score
- Variants: 2,671
- Variants ignored: 9
-
Trait: WA FA in tract superior longitudinal fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 2,464 (92.25%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001659
Reference score
- Variants: 187
- Variants ignored: 0
-
Trait: WA FA in tract uncinate fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 167 (89.3%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001660
Reference score
- Variants: 205
- Variants ignored: 0
-
Trait: WA FA in tract uncinate fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 186 (90.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001661
Reference score
- Variants: 1,563
- Variants ignored: 18
-
Trait: WA ICVF in tract acoustic radiation (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,439 (92.07%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001662
Reference score
- Variants: 979
- Variants ignored: 0
-
Trait: WA ICVF in tract acoustic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 887 (90.6%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001663
Reference score
- Variants: 817
- Variants ignored: 0
-
Trait: WA ICVF in tract anterior thalamic radiation (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 747 (91.43%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001664
Reference score
- Variants: 791
- Variants ignored: 0
-
Trait: WA ICVF in tract anterior thalamic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 725 (91.66%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001665
Reference score
- Variants: 1,095
- Variants ignored: 9
-
Trait: WA ICVF in tract cingulate gyrus part of cingulum (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,014 (92.6%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001666
Reference score
- Variants: 998
- Variants ignored: 0
-
Trait: WA ICVF in tract cingulate gyrus part of cingulum (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 916 (91.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001667
Reference score
- Variants: 1,128
- Variants ignored: 9
-
Trait: WA ICVF in tract corticospinal tract (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,006 (89.18%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001668
Reference score
- Variants: 310
- Variants ignored: 9
-
Trait: WA ICVF in tract corticospinal tract (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 276 (89.03%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001669
Reference score
- Variants: 1,466
- Variants ignored: 9
-
Trait: WA ICVF in tract forceps major
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,351 (92.16%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001670
Reference score
- Variants: 2,047
- Variants ignored: 9
-
Trait: WA ICVF in tract forceps minor
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,900 (92.82%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001671
Reference score
- Variants: 2,008
- Variants ignored: 9
-
Trait: WA ICVF in tract inferior fronto-occipital fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,850 (92.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001672
Reference score
- Variants: 1,964
- Variants ignored: 18
-
Trait: WA ICVF in tract inferior fronto-occipital fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,817 (92.52%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001673
Reference score
- Variants: 1,804
- Variants ignored: 18
-
Trait: WA ICVF in tract inferior longitudinal fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,663 (92.18%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001674
Reference score
- Variants: 1,872
- Variants ignored: 9
-
Trait: WA ICVF in tract inferior longitudinal fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,722 (91.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001675
Reference score
- Variants: 663
- Variants ignored: 0
-
Trait: WA ICVF in tract medial lemniscus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 601 (90.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001676
Reference score
- Variants: 600
- Variants ignored: 9
-
Trait: WA ICVF in tract medial lemniscus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 522 (87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001677
Reference score
- Variants: 512
- Variants ignored: 0
-
Trait: WA ICVF in tract middle cerebellar peduncle
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 454 (88.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001678
Reference score
- Variants: 449
- Variants ignored: 9
-
Trait: WA ICVF in tract parahippocampal part of cingulum (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 401 (89.31%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001679
Reference score
- Variants: 955
- Variants ignored: 9
-
Trait: WA ICVF in tract parahippocampal part of cingulum (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 858 (89.84%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001680
Reference score
- Variants: 1,264
- Variants ignored: 9
-
Trait: WA ICVF in tract posterior thalamic radiation (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,170 (92.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001681
Reference score
- Variants: 1,618
- Variants ignored: 27
-
Trait: WA ICVF in tract posterior thalamic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,494 (92.34%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001682
Reference score
- Variants: 2,131
- Variants ignored: 18
-
Trait: WA ICVF in tract superior longitudinal fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,974 (92.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001683
Reference score
- Variants: 1,652
- Variants ignored: 9
-
Trait: WA ICVF in tract superior longitudinal fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,525 (92.31%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001684
Reference score
- Variants: 1,165
- Variants ignored: 0
-
Trait: WA ICVF in tract superior thalamic radiation (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,047 (89.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001685
Reference score
- Variants: 1,474
- Variants ignored: 9
-
Trait: WA ICVF in tract superior thalamic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,344 (91.18%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001686
Reference score
- Variants: 136
- Variants ignored: 0
-
Trait: WA ICVF in tract uncinate fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 126 (92.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001687
Reference score
- Variants: 837
- Variants ignored: 0
-
Trait: WA ICVF in tract uncinate fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 763 (91.16%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001688
Reference score
- Variants: 231
- Variants ignored: 0
-
Trait: WA ISOVF in tract acoustic radiation (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 211 (91.34%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001689
Reference score
- Variants: 725
- Variants ignored: 9
-
Trait: WA ISOVF in tract acoustic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 659 (90.9%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001690
Reference score
- Variants: 130
- Variants ignored: 9
-
Trait: WA ISOVF in tract anterior thalamic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 111 (85.38%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001691
Reference score
- Variants: 477
- Variants ignored: 9
-
Trait: WA ISOVF in tract cingulate gyrus part of cingulum (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 429 (89.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001692
Reference score
- Variants: 245
- Variants ignored: 9
-
Trait: WA ISOVF in tract cingulate gyrus part of cingulum (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 210 (85.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001693
Reference score
- Variants: 1,080
- Variants ignored: 9
-
Trait: WA ISOVF in tract inferior fronto-occipital fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 969 (89.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001694
Reference score
- Variants: 1,146
- Variants ignored: 9
-
Trait: WA ISOVF in tract inferior fronto-occipital fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,024 (89.35%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001695
Reference score
- Variants: 1,123
- Variants ignored: 9
-
Trait: WA ISOVF in tract inferior longitudinal fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,011 (90.03%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001696
Reference score
- Variants: 1,688
- Variants ignored: 9
-
Trait: WA ISOVF in tract inferior longitudinal fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,560 (92.42%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001697
Reference score
- Variants: 72
- Variants ignored: 0
-
Trait: WA ISOVF in tract posterior thalamic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 61 (84.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001698
Reference score
- Variants: 695
- Variants ignored: 9
-
Trait: WA ISOVF in tract superior longitudinal fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 637 (91.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001699
Reference score
- Variants: 197
- Variants ignored: 9
-
Trait: WA ISOVF in tract superior longitudinal fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 175 (88.83%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001700
Reference score
- Variants: 538
- Variants ignored: 9
-
Trait: WA ISOVF in tract superior thalamic radiation (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 489 (90.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001701
Reference score
- Variants: 174
- Variants ignored: 9
-
Trait: WA ISOVF in tract superior thalamic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 153 (87.93%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001702
Reference score
- Variants: 385
- Variants ignored: 9
-
Trait: WA ISOVF in tract uncinate fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 332 (86.23%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001703
Reference score
- Variants: 83
- Variants ignored: 0
-
Trait: WA ISOVF in tract uncinate fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 72 (86.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001704
Reference score
- Variants: 514
- Variants ignored: 0
-
Trait: WA L1 in tract forceps minor
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 461 (89.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001705
Reference score
- Variants: 547
- Variants ignored: 0
-
Trait: WA L1 in tract inferior fronto-occipital fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 476 (87.02%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001706
Reference score
- Variants: 322
- Variants ignored: 0
-
Trait: WA L1 in tract inferior fronto-occipital fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 279 (86.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001707
Reference score
- Variants: 499
- Variants ignored: 0
-
Trait: WA L1 in tract inferior longitudinal fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 439 (87.98%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001708
Reference score
- Variants: 316
- Variants ignored: 0
-
Trait: WA L1 in tract inferior longitudinal fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 276 (87.34%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001709
Reference score
- Variants: 1,382
- Variants ignored: 0
-
Trait: WA L1 in tract superior longitudinal fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,274 (92.19%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001710
Reference score
- Variants: 534
- Variants ignored: 0
-
Trait: WA L1 in tract superior longitudinal fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 484 (90.64%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001711
Reference score
- Variants: 457
- Variants ignored: 0
-
Trait: WA L1 in tract superior thalamic radiation (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 409 (89.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001712
Reference score
- Variants: 358
- Variants ignored: 0
-
Trait: WA L1 in tract superior thalamic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 311 (86.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001713
Reference score
- Variants: 173
- Variants ignored: 0
-
Trait: WA L1 in tract uncinate fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 151 (87.28%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001714
Reference score
- Variants: 993
- Variants ignored: 0
-
Trait: WA L2 in tract acoustic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 884 (89.02%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001715
Reference score
- Variants: 170
- Variants ignored: 9
-
Trait: WA L2 in tract anterior thalamic radiation (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 144 (84.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001716
Reference score
- Variants: 290
- Variants ignored: 0
-
Trait: WA L2 in tract anterior thalamic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 255 (87.93%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001717
Reference score
- Variants: 82
- Variants ignored: 0
-
Trait: WA L2 in tract cingulate gyrus part of cingulum (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 75 (91.46%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001718
Reference score
- Variants: 305
- Variants ignored: 0
-
Trait: WA L2 in tract cingulate gyrus part of cingulum (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 272 (89.18%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001719
Reference score
- Variants: 924
- Variants ignored: 0
-
Trait: WA L2 in tract forceps major
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 848 (91.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001720
Reference score
- Variants: 1,030
- Variants ignored: 0
-
Trait: WA L2 in tract forceps minor
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 945 (91.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001721
Reference score
- Variants: 691
- Variants ignored: 0
-
Trait: WA L2 in tract inferior fronto-occipital fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 600 (86.83%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001722
Reference score
- Variants: 814
- Variants ignored: 0
-
Trait: WA L2 in tract inferior fronto-occipital fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 727 (89.31%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001723
Reference score
- Variants: 711
- Variants ignored: 0
-
Trait: WA L2 in tract inferior longitudinal fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 636 (89.45%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001724
Reference score
- Variants: 793
- Variants ignored: 0
-
Trait: WA L2 in tract inferior longitudinal fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 723 (91.17%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001725
Reference score
- Variants: 1,749
- Variants ignored: 0
-
Trait: WA L2 in tract superior longitudinal fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,619 (92.57%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001726
Reference score
- Variants: 683
- Variants ignored: 0
-
Trait: WA L2 in tract superior thalamic radiation (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 623 (91.22%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001727
Reference score
- Variants: 709
- Variants ignored: 0
-
Trait: WA L2 in tract uncinate fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 640 (90.27%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001728
Reference score
- Variants: 706
- Variants ignored: 0
-
Trait: WA L2 in tract uncinate fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 641 (90.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001729
Reference score
- Variants: 794
- Variants ignored: 0
-
Trait: WA L3 in tract acoustic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 709 (89.29%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001730
Reference score
- Variants: 200
- Variants ignored: 0
-
Trait: WA L3 in tract anterior thalamic radiation (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 173 (86.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001731
Reference score
- Variants: 432
- Variants ignored: 0
-
Trait: WA L3 in tract anterior thalamic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 391 (90.51%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001732
Reference score
- Variants: 1,611
- Variants ignored: 0
-
Trait: WA L3 in tract cingulate gyrus part of cingulum (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,466 (91%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001733
Reference score
- Variants: 1,080
- Variants ignored: 0
-
Trait: WA L3 in tract cingulate gyrus part of cingulum (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 976 (90.37%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001734
Reference score
- Variants: 1,536
- Variants ignored: 0
-
Trait: WA L3 in tract forceps minor
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,417 (92.25%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001735
Reference score
- Variants: 945
- Variants ignored: 0
-
Trait: WA L3 in tract inferior fronto-occipital fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 856 (90.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001736
Reference score
- Variants: 864
- Variants ignored: 0
-
Trait: WA L3 in tract inferior fronto-occipital fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 773 (89.47%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001737
Reference score
- Variants: 919
- Variants ignored: 0
-
Trait: WA L3 in tract inferior longitudinal fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 834 (90.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001738
Reference score
- Variants: 825
- Variants ignored: 0
-
Trait: WA L3 in tract inferior longitudinal fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 749 (90.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001739
Reference score
- Variants: 1,884
- Variants ignored: 0
-
Trait: WA L3 in tract superior longitudinal fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,744 (92.57%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001740
Reference score
- Variants: 855
- Variants ignored: 0
-
Trait: WA L3 in tract superior thalamic radiation (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 773 (90.41%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001741
Reference score
- Variants: 1,510
- Variants ignored: 0
-
Trait: WA L3 in tract superior thalamic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,386 (91.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001742
Reference score
- Variants: 755
- Variants ignored: 0
-
Trait: WA L3 in tract uncinate fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 689 (91.26%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001743
Reference score
- Variants: 1,320
- Variants ignored: 0
-
Trait: WA L3 in tract uncinate fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,199 (90.83%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001744
Reference score
- Variants: 315
- Variants ignored: 0
-
Trait: WA MD in tract acoustic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 264 (83.81%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001745
Reference score
- Variants: 171
- Variants ignored: 9
-
Trait: WA MD in tract anterior thalamic radiation (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 150 (87.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001746
Reference score
- Variants: 296
- Variants ignored: 0
-
Trait: WA MD in tract cingulate gyrus part of cingulum (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 267 (90.2%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001747
Reference score
- Variants: 767
- Variants ignored: 0
-
Trait: WA MD in tract cingulate gyrus part of cingulum (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 687 (89.57%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001748
Reference score
- Variants: 209
- Variants ignored: 0
-
Trait: WA MD in tract forceps major
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 186 (89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001749
Reference score
- Variants: 1,164
- Variants ignored: 0
-
Trait: WA MD in tract forceps minor
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,056 (90.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001750
Reference score
- Variants: 813
- Variants ignored: 0
-
Trait: WA MD in tract inferior fronto-occipital fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 728 (89.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001751
Reference score
- Variants: 702
- Variants ignored: 0
-
Trait: WA MD in tract inferior fronto-occipital fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 617 (87.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001752
Reference score
- Variants: 572
- Variants ignored: 0
-
Trait: WA MD in tract inferior longitudinal fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 514 (89.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001753
Reference score
- Variants: 975
- Variants ignored: 0
-
Trait: WA MD in tract inferior longitudinal fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 885 (90.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001754
Reference score
- Variants: 1,809
- Variants ignored: 0
-
Trait: WA MD in tract superior longitudinal fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,674 (92.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001755
Reference score
- Variants: 610
- Variants ignored: 0
-
Trait: WA MD in tract superior thalamic radiation (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 539 (88.36%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001756
Reference score
- Variants: 96
- Variants ignored: 0
-
Trait: WA MD in tract superior thalamic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 81 (84.38%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001757
Reference score
- Variants: 872
- Variants ignored: 0
-
Trait: WA MD in tract uncinate fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 798 (91.51%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001758
Reference score
- Variants: 1,033
- Variants ignored: 0
-
Trait: WA MD in tract uncinate fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 938 (90.8%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001759
Reference score
- Variants: 1,836
- Variants ignored: 0
-
Trait: WA MO in tract forceps minor
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,700 (92.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001760
Reference score
- Variants: 258
- Variants ignored: 0
-
Trait: WA MO in tract medial lemniscus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 225 (87.21%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001761
Reference score
- Variants: 47
- Variants ignored: 0
-
Trait: WA MO in tract middle cerebellar peduncle
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 37 (78.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001762
Reference score
- Variants: 721
- Variants ignored: 0
-
Trait: WA MO in tract posterior thalamic radiation (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 645 (89.46%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001763
Reference score
- Variants: 342
- Variants ignored: 0
-
Trait: WA MO in tract posterior thalamic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 309 (90.35%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001764
Reference score
- Variants: 961
- Variants ignored: 0
-
Trait: WA MO in tract superior longitudinal fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 874 (90.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001765
Reference score
- Variants: 1,023
- Variants ignored: 0
-
Trait: WA MO in tract superior thalamic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 928 (90.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001766
Reference score
- Variants: 1
- Variants ignored: 0
-
Trait: WA OD in tract corticospinal tract (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001767
Reference score
- Variants: 378
- Variants ignored: 0
-
Trait: WA OD in tract inferior longitudinal fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 339 (89.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001768
Reference score
- Variants: 297
- Variants ignored: 0
-
Trait: WA OD in tract medial lemniscus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 263 (88.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001769
Reference score
- Variants: 1,298
- Variants ignored: 0
-
Trait: WA OD in tract superior longitudinal fasciculus (L)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,175 (90.52%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001770
Reference score
- Variants: 726
- Variants ignored: 0
-
Trait: WA OD in tract superior longitudinal fasciculus (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 656 (90.36%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001771
Reference score
- Variants: 1,352
- Variants ignored: 0
-
Trait: WA OD in tract superior thalamic radiation (R)
- Mapped Trait(s):
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 1,239 (91.64%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001772
Reference score
- Variants: 158
- Variants ignored: 18
-
Trait: ZEBRA antigen for Epstein-Barr Virus
- Mapped Trait(s):
- EFO_0009273: anti-Epstein Barr virus antibody measurement
- Publication: Tanigawa Y et.al, PLoS Genet (2022-03-24)
- View in PGS-Catalog
Target study
- Coverage: 132 (83.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001773
Reference score
- Variants: 25
- Variants ignored: 0
-
Trait: Moderate-to-severe atopic dermatitis
- Mapped Trait(s):
- Samples: 2,688
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Simard M et.al, J Allergy Clin Immunol (2020-05-19)
- View in PGS-Catalog
Target study
- Coverage: 23 (92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001774
Reference score
- Variants: 12
- Variants ignored: 0
-
Trait: Parkinson's disease
- Mapped Trait(s):
- Samples: 158,108
- Population:
- Publication: Chairta PP et.al, Genes (Basel) (2021-08-20)
- View in PGS-Catalog
Target study
- Coverage: 12 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001775
Reference score
- Variants: 39
- Variants ignored: 0
-
Trait: Alzheimer's disease
- Mapped Trait(s):
- Samples: 98,100
- Population:
- Publication: Ebenau JL et.al, Alzheimers Dement (Amst) (2021-09-14)
- View in PGS-Catalog
Target study
- Coverage: 38 (97.44%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001776
Reference score
- Variants: 45
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 250,737
- Population:
- European: 93.7%
- East Asian: 4.9%
- Unknown: 0.9%
- Additional Diverse Ancestries: 0.4%
- Multi-Ancestry (excluding Europeans): 0.2%
- Publication: Gafni A et.al, PLoS One (2021-09-15)
- View in PGS-Catalog
Target study
- Coverage: 45 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001777
Reference score
- Variants: 3
- Variants ignored: 0
-
Trait: Cirrhosis (alcohol related)
- Mapped Trait(s):
- Samples: 48,682
- Population:
- Publication: Whitfield JB et.al, J Hepatol (2021-10-13)
- View in PGS-Catalog
Target study
- Coverage: 3 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001778
Reference score
- Variants: 15
- Variants ignored: 0
-
Trait: Breast cancer
- Mapped Trait(s):
- Samples: 98,087
- Population:
- Multi-Ancestry (including Europeans): 70.9%
- European: 26%
- East Asian: 3.1%
- Publication: Yiangou K et.al, Cancers (Basel) (2021-09-11)
- View in PGS-Catalog
Target study
- Coverage: 15 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001779
Reference score
- Variants: 21
- Variants ignored: 0
-
Trait: Brugada syndrome
- Mapped Trait(s):
- Samples: 12,821
- Population:
- Publication: Barc J et.al, Nat Genet (2022-02-24)
- View in PGS-Catalog
Target study
- Coverage: 21 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001780
Reference score
- Variants: 1,090,048
- Variants ignored: 0
-
Trait: Coronary heart disease
- Mapped Trait(s):
- Samples: 187,599
- Population:
- European: 75.3%
- South Asian: 13.6%
- East Asian: 6%
- Hispanic or Latin American: 2.2%
- African: 1.7%
- Greater Middle Eastern: 1.2%
- Publication: Tamlander M et.al, Commun Biol (2022-02-23)
- View in PGS-Catalog
Target study
- Coverage: 1,089,642 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001781
Reference score
- Variants: 1,091,673
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 159,208
- Population:
- Publication: Tamlander M et.al, Commun Biol (2022-02-23)
- View in PGS-Catalog
Target study
- Coverage: 1,091,671 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001782
Reference score
- Variants: 884,043
- Variants ignored: 0
-
Trait: Asthma
- Mapped Trait(s):
- Samples: 1,800,785
- Population:
- European: 76.4%
- East Asian: 18.9%
- African: 1.8%
- Additional Asian Ancestries: 1.7%
- Additional Diverse Ancestries: 1%
- Greater Middle Eastern: 0.09%
- Publication: Wang Y et.al, medRxiv (2021-11-21)
- View in PGS-Catalog
Target study
- Coverage: 884,043 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001783
Reference score
- Variants: 884,139
- Variants ignored: 0
-
Trait: Chronic obstructive pulmonary disease
- Mapped Trait(s):
- Samples: 1,392,366
- Population:
- European: 71.5%
- East Asian: 23.7%
- African: 2.1%
- Additional Asian Ancestries: 1.6%
- Additional Diverse Ancestries: 1.1%
- Publication: Wang Y et.al, medRxiv (2021-11-21)
- View in PGS-Catalog
Target study
- Coverage: 884,139 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001784
Reference score
- Variants: 911,440
- Variants ignored: 0
-
Trait: Abdominal aortic aneurysm
- Mapped Trait(s):
- Samples: 1,046,004
- Population:
- European: 81.7%
- East Asian: 16.7%
- Additional Diverse Ancestries: 0.9%
- African: 0.6%
- Publication: Wang Y et.al, medRxiv (2021-11-21)
- View in PGS-Catalog
Target study
- Coverage: 911,440 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001785
Reference score
- Variants: 911,334
- Variants ignored: 0
-
Trait: Acute appendicitis
- Mapped Trait(s):
- Samples: 688,784
- Population:
- European: 85.7%
- East Asian: 11%
- Additional Asian Ancestries: 3.2%
- Publication: Wang Y et.al, medRxiv (2021-11-21)
- View in PGS-Catalog
Target study
- Coverage: 911,334 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001786
Reference score
- Variants: 899,660
- Variants ignored: 0
-
Trait: Appendectomy
- Mapped Trait(s):
- Samples: 357,072
- Population:
- Publication: Wang Y et.al, medRxiv (2021-11-21)
- View in PGS-Catalog
Target study
- Coverage: 899,660 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001787
Reference score
- Variants: 909,990
- Variants ignored: 0
-
Trait: Asthma
- Mapped Trait(s):
- Samples: 1,369,372
- Population:
- European: 70.5%
- East Asian: 24.7%
- African: 1.9%
- Additional Asian Ancestries: 1.6%
- Additional Diverse Ancestries: 1.3%
- Publication: Wang Y et.al, medRxiv (2021-11-21)
- View in PGS-Catalog
Target study
- Coverage: 909,990 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001788
Reference score
- Variants: 910,082
- Variants ignored: 0
-
Trait: Chronic obstructive pulmonary disease
- Mapped Trait(s):
- Samples: 992,289
- Population:
- European: 60.7%
- East Asian: 33.2%
- African: 2.4%
- Additional Asian Ancestries: 2.2%
- Additional Diverse Ancestries: 1.5%
- Publication: Wang Y et.al, medRxiv (2021-11-21)
- View in PGS-Catalog
Target study
- Coverage: 910,082 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001789
Reference score
- Variants: 910,151
- Variants ignored: 0
-
Trait: Gout
- Mapped Trait(s):
- Samples: 1,049,659
- Population:
- European: 60.2%
- East Asian: 33.3%
- African: 2.7%
- Additional Asian Ancestries: 2.1%
- Additional Diverse Ancestries: 1.7%
- Publication: Wang Y et.al, medRxiv (2021-11-21)
- View in PGS-Catalog
Target study
- Coverage: 910,151 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001790
Reference score
- Variants: 910,146
- Variants ignored: 0
-
Trait: Heart Failure
- Mapped Trait(s):
- Samples: 919,746
- Population:
- European: 65.3%
- East Asian: 28%
- African: 2.7%
- Additional Asian Ancestries: 2.4%
- Additional Diverse Ancestries: 1.6%
- Publication: Wang Y et.al, medRxiv (2021-11-21)
- View in PGS-Catalog
Target study
- Coverage: 910,146 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001791
Reference score
- Variants: 910,439
- Variants ignored: 0
-
Trait: Idiopathic pulmonary fibrosis
- Mapped Trait(s):
- Samples: 848,799
- Population:
- European: 64.6%
- East Asian: 30.1%
- Additional Asian Ancestries: 2.6%
- Additional Diverse Ancestries: 1.7%
- African: 1%
- Publication: Wang Y et.al, medRxiv (2021-11-21)
- View in PGS-Catalog
Target study
- Coverage: 910,439 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001792
Reference score
- Variants: 911,402
- Variants ignored: 0
-
Trait: Primary open-angle glaucoma
- Mapped Trait(s):
- Samples: 1,066,654
- Population:
- European: 71.9%
- East Asian: 25.3%
- African: 1.9%
- Additional Diverse Ancestries: 0.9%
- Publication: Wang Y et.al, medRxiv (2021-11-21)
- View in PGS-Catalog
Target study
- Coverage: 911,402 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001793
Reference score
- Variants: 910,099
- Variants ignored: 0
-
Trait: Stroke
- Mapped Trait(s):
- Samples: 939,362
- Population:
- European: 67%
- East Asian: 28.6%
- African: 2.7%
- Additional Diverse Ancestries: 1.6%
- Publication: Wang Y et.al, medRxiv (2021-11-21)
- View in PGS-Catalog
Target study
- Coverage: 910,099 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001794
Reference score
- Variants: 911,462
- Variants ignored: 0
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Samples: 1,201,302
- Population:
- European: 76.6%
- East Asian: 21.2%
- African: 1.2%
- Additional Diverse Ancestries: 0.9%
- Publication: Wang Y et.al, medRxiv (2021-11-21)
- View in PGS-Catalog
Target study
- Coverage: 911,462 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001795
Reference score
- Variants: 911,692
- Variants ignored: 0
-
Trait: Uterine cancer
- Mapped Trait(s):
- Samples: 692,891
- Population:
- European: 83.9%
- East Asian: 15.2%
- Additional Diverse Ancestries: 0.8%
- Publication: Wang Y et.al, medRxiv (2021-11-21)
- View in PGS-Catalog
Target study
- Coverage: 911,692 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001796
Reference score
- Variants: 910,337
- Variants ignored: 0
-
Trait: Venous thromboembolism
- Mapped Trait(s):
- Samples: 628,261
- Population:
- European: 79%
- East Asian: 12.4%
- African: 4.1%
- Additional Asian Ancestries: 2.4%
- Additional Diverse Ancestries: 2.2%
- Publication: Wang Y et.al, medRxiv (2021-11-21)
- View in PGS-Catalog
Target study
- Coverage: 910,337 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001797
Reference score
- Variants: 885,417
- Variants ignored: 0
-
Trait: Primary open-angle glaucoma
- Mapped Trait(s):
- Samples: 1,487,447
- Population:
- European: 78.9%
- East Asian: 18.1%
- African: 1.8%
- Additional Diverse Ancestries: 0.6%
- Additional Asian Ancestries: 0.6%
- Publication: Wang Y et.al, medRxiv (2021-11-21)
- View in PGS-Catalog
Target study
- Coverage: 885,417 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001798
Reference score
- Variants: 884,168
- Variants ignored: 0
-
Trait: Stroke
- Mapped Trait(s):
- Samples: 1,370,901
- Population:
- European: 75.8%
- East Asian: 19.6%
- African: 1.9%
- Additional Asian Ancestries: 1.6%
- Additional Diverse Ancestries: 1.1%
- Publication: Wang Y et.al, medRxiv (2021-11-21)
- View in PGS-Catalog
Target study
- Coverage: 884,168 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001799
Reference score
- Variants: 885,482
- Variants ignored: 0
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Samples: 1,620,354
- Population:
- European: 82.7%
- East Asian: 15.7%
- African: 0.9%
- Additional Diverse Ancestries: 0.7%
- Publication: Wang Y et.al, medRxiv (2021-11-21)
- View in PGS-Catalog
Target study
- Coverage: 885,482 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001800
Reference score
- Variants: 1,713,430
- Variants ignored: 0
-
Trait: Forced expiratory volume (FEV1)
- Mapped Trait(s):
- Samples: 321,047
- Population:
- Publication: Moll M et.al, Lancet Respir Med (2020-07-01)
- View in PGS-Catalog
Target study
- Coverage: 1,707,289 (99.64%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001801
Reference score
- Variants: 1,232,916
- Variants ignored: 0
-
Trait: FEV1/FVC ratio
- Mapped Trait(s):
- Samples: 321,047
- Population:
- Publication: Moll M et.al, Lancet Respir Med (2020-07-01)
- View in PGS-Catalog
Target study
- Coverage: 1,228,304 (99.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001802
Reference score
- Variants: 2,821
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 2,821 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001803
Reference score
- Variants: 4,371
- Variants ignored: 0
-
Trait: Skin cancer
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 4,371 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001804
Reference score
- Variants: 2,984
- Variants ignored: 0
-
Trait: Breast cancer [female]
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 2,984 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001805
Reference score
- Variants: 2,579
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 2,579 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001806
Reference score
- Variants: 231
- Variants ignored: 0
-
Trait: Malignant neoplasm of testis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 231 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001807
Reference score
- Variants: 291
- Variants ignored: 0
-
Trait: Cancer of bladder
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 291 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001808
Reference score
- Variants: 117
- Variants ignored: 0
-
Trait: Cancer of brain
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 117 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001809
Reference score
- Variants: 111
- Variants ignored: 0
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 111 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001810
Reference score
- Variants: 67
- Variants ignored: 0
-
Trait: Polycythemia vera
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 67 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001811
Reference score
- Variants: 2,231
- Variants ignored: 0
-
Trait: Benign neoplasm of colon
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 2,231 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001812
Reference score
- Variants: 801
- Variants ignored: 0
-
Trait: Benign neoplasm of other parts of digestive system
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 801 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001813
Reference score
- Variants: 1,308
- Variants ignored: 0
-
Trait: Benign neoplasm of uterus
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 1,308 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001814
Reference score
- Variants: 322
- Variants ignored: 0
-
Trait: Nontoxic multinodular goiter
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 322 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001815
Reference score
- Variants: 280
- Variants ignored: 0
-
Trait: Thyrotoxicosis with or without goiter
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 280 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001816
Reference score
- Variants: 11,130
- Variants ignored: 0
-
Trait: Hypothyroidism
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 11,130 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001817
Reference score
- Variants: 825
- Variants ignored: 0
-
Trait: Type 1 diabetes
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 825 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001818
Reference score
- Variants: 30,745
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 30,745 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001819
Reference score
- Variants: 249
- Variants ignored: 0
-
Trait: Diabetic retinopathy
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 249 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001820
Reference score
- Variants: 187
- Variants ignored: 0
-
Trait: Hypoglycemia
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 187 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001821
Reference score
- Variants: 22,313
- Variants ignored: 0
-
Trait: Disorders of lipoid metabolism
- Mapped Trait(s):
- HP_0003119: Abnormal circulating lipid concentration
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 22,313 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001822
Reference score
- Variants: 216
- Variants ignored: 0
-
Trait: Gout
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 216 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001823
Reference score
- Variants: 654
- Variants ignored: 0
-
Trait: Disorders of iron metabolism
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 654 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001824
Reference score
- Variants: 22
- Variants ignored: 0
-
Trait: Disorders of bilirubin excretion
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 22 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001825
Reference score
- Variants: 13,009
- Variants ignored: 0
-
Trait: Overweight, obesity and other hyperalimentation
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 13,009 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001826
Reference score
- Variants: 45
- Variants ignored: 0
-
Trait: Congenital deficiency of other clotting factors (including factor VII)
- Mapped Trait(s):
- MONDO_0015722: congenital vitamin K-dependent coagulation factors deficiency
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 45 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001827
Reference score
- Variants: 33
- Variants ignored: 0
-
Trait: Dementias
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 33 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001828
Reference score
- Variants: 38
- Variants ignored: 0
-
Trait: Alzheimer's disease
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 38 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001829
Reference score
- Variants: 7,534
- Variants ignored: 0
-
Trait: Depression
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 7,534 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001830
Reference score
- Variants: 13,838
- Variants ignored: 0
-
Trait: Tobacco use disorder
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 13,838 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001831
Reference score
- Variants: 491
- Variants ignored: 0
-
Trait: Multiple sclerosis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 491 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001832
Reference score
- Variants: 8,393
- Variants ignored: 0
-
Trait: Other peripheral nerve disorders
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 8,393 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001833
Reference score
- Variants: 3,737
- Variants ignored: 0
-
Trait: Retinal detachments and defects
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 3,737 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001834
Reference score
- Variants: 157
- Variants ignored: 0
-
Trait: Macular degeneration (senile) of retina NOS
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 157 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001835
Reference score
- Variants: 38
- Variants ignored: 0
-
Trait: Corneal dystrophy
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 38 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001836
Reference score
- Variants: 7,052
- Variants ignored: 0
-
Trait: Glaucoma
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 7,052 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001837
Reference score
- Variants: 11,617
- Variants ignored: 0
-
Trait: Cataract
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 11,617 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001838
Reference score
- Variants: 52,487
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 52,487 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001839
Reference score
- Variants: 25,425
- Variants ignored: 0
-
Trait: Coronary atherosclerosis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 25,425 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001840
Reference score
- Variants: 330
- Variants ignored: 0
-
Trait: Pulmonary heart disease
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 330 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001841
Reference score
- Variants: 3,980
- Variants ignored: 0
-
Trait: Atrial fibrillation and flutter
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 3,980 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001842
Reference score
- Variants: 2,759
- Variants ignored: 0
-
Trait: Congestive heart failure; nonhypertensive
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 2,759 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001843
Reference score
- Variants: 242
- Variants ignored: 0
-
Trait: Peripheral vascular disease, unspecified
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 242 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001844
Reference score
- Variants: 431
- Variants ignored: 0
-
Trait: Phlebitis and thrombophlebitis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 431 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001845
Reference score
- Variants: 15,748
- Variants ignored: 0
-
Trait: Varicose veins
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 15,748 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001846
Reference score
- Variants: 5,434
- Variants ignored: 0
-
Trait: Hemorrhoids
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 5,434 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001847
Reference score
- Variants: 594
- Variants ignored: 0
-
Trait: Circulatory disease NEC
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 594 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001848
Reference score
- Variants: 1,783
- Variants ignored: 0
-
Trait: Nasal polyps
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 1,783 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001849
Reference score
- Variants: 22,679
- Variants ignored: 0
-
Trait: Asthma
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 22,679 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001850
Reference score
- Variants: 7,347
- Variants ignored: 0
-
Trait: Chronic airway obstruction
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 7,347 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001851
Reference score
- Variants: 13,855
- Variants ignored: 0
-
Trait: Esophagitis, GERD and related diseases
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 13,855 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001852
Reference score
- Variants: 191
- Variants ignored: 0
-
Trait: Duodenitis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 191 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001853
Reference score
- Variants: 19
- Variants ignored: 0
-
Trait: Appendiceal conditions
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 19 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001854
Reference score
- Variants: 7,326
- Variants ignored: 0
-
Trait: Inguinal hernia
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 7,326 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001855
Reference score
- Variants: 1,505
- Variants ignored: 0
-
Trait: Ulcerative colitis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 1,505 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001856
Reference score
- Variants: 1,661
- Variants ignored: 0
-
Trait: Celiac disease
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 1,661 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001857
Reference score
- Variants: 23,800
- Variants ignored: 0
-
Trait: Diverticulosis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 23,800 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001858
Reference score
- Variants: 764
- Variants ignored: 0
-
Trait: Functional digestive disorders
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 764 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001859
Reference score
- Variants: 789
- Variants ignored: 0
-
Trait: Anal and rectal polyp
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 789 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001860
Reference score
- Variants: 497
- Variants ignored: 0
-
Trait: Other chronic nonalcoholic liver disease
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 497 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001861
Reference score
- Variants: 2,059
- Variants ignored: 0
-
Trait: Cholelithiasis and cholecystitis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 2,059 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001862
Reference score
- Variants: 151
- Variants ignored: 0
-
Trait: Other biliary tract disease
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 151 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001863
Reference score
- Variants: 794
- Variants ignored: 0
-
Trait: Hematuria
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 794 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001864
Reference score
- Variants: 5,599
- Variants ignored: 0
-
Trait: Urinary calculus
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 5,599 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001865
Reference score
- Variants: 1,712
- Variants ignored: 0
-
Trait: Hyperplasia of prostate
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 1,712 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001866
Reference score
- Variants: 399
- Variants ignored: 0
-
Trait: Endometriosis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 399 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001867
Reference score
- Variants: 9,708
- Variants ignored: 0
-
Trait: Genital prolapse
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 9,708 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001868
Reference score
- Variants: 30
- Variants ignored: 0
-
Trait: Rhesus isoimmunization in pregnancy
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 30 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001869
Reference score
- Variants: 131
- Variants ignored: 0
-
Trait: Superficial cellulitis and abscess
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 131 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001870
Reference score
- Variants: 87
- Variants ignored: 0
-
Trait: Lupus (localized and systemic)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 87 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001871
Reference score
- Variants: 264
- Variants ignored: 0
-
Trait: Psoriasis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 264 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001872
Reference score
- Variants: 79
- Variants ignored: 0
-
Trait: Sarcoidosis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 79 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001873
Reference score
- Variants: 461
- Variants ignored: 0
-
Trait: Diseases of hair and hair follicles
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 461 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001874
Reference score
- Variants: 563
- Variants ignored: 0
-
Trait: Sebaceous cyst
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 563 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001875
Reference score
- Variants: 256
- Variants ignored: 0
-
Trait: Rheumatoid arthritis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 256 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001876
Reference score
- Variants: 85
- Variants ignored: 0
-
Trait: Ankylosing spondylitis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 85 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001877
Reference score
- Variants: 17,363
- Variants ignored: 0
-
Trait: Other arthropathies
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 17,363 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001878
Reference score
- Variants: 142
- Variants ignored: 0
-
Trait: Polymyalgia Rheumatica
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 142 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001879
Reference score
- Variants: 210
- Variants ignored: 0
-
Trait: Ganglion and cyst of synovium, tendon, and bursa
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 210 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001880
Reference score
- Variants: 2,443
- Variants ignored: 0
-
Trait: Contracture of palmar fascia [Dupuytren's disease]
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 2,443 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001881
Reference score
- Variants: 4,527
- Variants ignored: 0
-
Trait: Hallux valgus (Bunion)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 4,527 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001882
Reference score
- Variants: 11,451
- Variants ignored: 0
-
Trait: Osteoarthrosis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 11,451 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001883
Reference score
- Variants: 365
- Variants ignored: 0
-
Trait: Osteoporosis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 365 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001884
Reference score
- Variants: 2,796
- Variants ignored: 0
-
Trait: Abdominal pain
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 2,796 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001885
Reference score
- Variants: 95
- Variants ignored: 0
-
Trait: Allergy/adverse effect of penicillin
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 95 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001886
Reference score
- Variants: 60,423
- Variants ignored: 0
-
Trait: Albumin
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 60,423 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001887
Reference score
- Variants: 89,827
- Variants ignored: 0
-
Trait: Ankle spacing width
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 89,827 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001888
Reference score
- Variants: 74,596
- Variants ignored: 0
-
Trait: Apolipoprotein A
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 74,596 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001889
Reference score
- Variants: 16,952
- Variants ignored: 0
-
Trait: Apolipoprotein B
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 16,952 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001890
Reference score
- Variants: 44,864
- Variants ignored: 0
-
Trait: avMSE
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 44,864 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001891
Reference score
- Variants: 19,960
- Variants ignored: 0
-
Trait: Hearing difficulty/problems
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 19,960 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001892
Reference score
- Variants: 35,060
- Variants ignored: 0
-
Trait: Birth weight
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 35,060 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001893
Reference score
- Variants: 48,395
- Variants ignored: 0
-
Trait: Calcium
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 48,395 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001894
Reference score
- Variants: 484
- Variants ignored: 0
-
Trait: Diagnosed with coeliac disease or gluten sensitivity
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 484 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001895
Reference score
- Variants: 16,576
- Variants ignored: 0
-
Trait: Cholesterol
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 16,576 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001896
Reference score
- Variants: 31,036
- Variants ignored: 0
-
Trait: Hair colour (natural, before greying)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 31,036 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001897
Reference score
- Variants: 15,817
- Variants ignored: 0
-
Trait: Skin colour
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 15,817 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001898
Reference score
- Variants: 5,777
- Variants ignored: 0
-
Trait: Ever depressed for a whole week
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 5,777 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001899
Reference score
- Variants: 2,434
- Variants ignored: 0
-
Trait: Recent feelings of depression
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 2,434 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001900
Reference score
- Variants: 66,335
- Variants ignored: 0
-
Trait: Diastolic blood pressure, automated reading
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 66,335 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001901
Reference score
- Variants: 1,065
- Variants ignored: 0
-
Trait: Alcohol drinker status
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 1,065 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001902
Reference score
- Variants: 640
- Variants ignored: 0
-
Trait: P duration
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 640 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001903
Reference score
- Variants: 4,368
- Variants ignored: 0
-
Trait: PP interval
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 4,368 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001904
Reference score
- Variants: 826
- Variants ignored: 0
-
Trait: PQ interval
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 826 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001905
Reference score
- Variants: 2,300
- Variants ignored: 0
-
Trait: QT interval
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 2,300 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001906
Reference score
- Variants: 641
- Variants ignored: 0
-
Trait: QTC interval
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 641 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001907
Reference score
- Variants: 1,964
- Variants ignored: 0
-
Trait: RR interval
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 1,964 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001908
Reference score
- Variants: 32,431
- Variants ignored: 0
-
Trait: Red blood cell (erythrocyte) distribution width
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 32,431 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001909
Reference score
- Variants: 81,887
- Variants ignored: 0
-
Trait: Red blood cell (erythrocyte) count
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 81,887 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001910
Reference score
- Variants: 9,341
- Variants ignored: 0
-
Trait: Ever taken cannabis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 9,341 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001911
Reference score
- Variants: 41,266
- Variants ignored: 0
-
Trait: Ever smoked
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 41,266 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001912
Reference score
- Variants: 15,201
- Variants ignored: 0
-
Trait: Age at first live birth
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 15,201 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001913
Reference score
- Variants: 339
- Variants ignored: 0
-
Trait: Length of menstrual cycle
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 339 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001914
Reference score
- Variants: 18,179
- Variants ignored: 0
-
Trait: Testosterone (female only)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 18,179 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001915
Reference score
- Variants: 38,940
- Variants ignored: 0
-
Trait: Age when periods started (menarche)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 38,940 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001916
Reference score
- Variants: 9,917
- Variants ignored: 0
-
Trait: Falls in the last year
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 9,917 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001917
Reference score
- Variants: 107,244
- Variants ignored: 0
-
Trait: Body fat percentage
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 107,244 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001918
Reference score
- Variants: 79,136
- Variants ignored: 0
-
Trait: Forced expiratory volume in 1-second (FEV1), Best measure
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 79,136 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001919
Reference score
- Variants: 26,145
- Variants ignored: 0
-
Trait: Fluid intelligence score
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 26,145 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001920
Reference score
- Variants: 2,894
- Variants ignored: 0
-
Trait: Recent feelings of foreboding
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 2,894 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001921
Reference score
- Variants: 7,965
- Variants ignored: 0
-
Trait: Fractured/broken bones in last 5 years
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 7,965 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001922
Reference score
- Variants: 85,349
- Variants ignored: 0
-
Trait: Forced vital capacity (FVC), Best measure
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 85,349 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001923
Reference score
- Variants: 50,583
- Variants ignored: 0
-
Trait: Time spent watching television (TV) or using computer
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 50,583 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001924
Reference score
- Variants: 311
- Variants ignored: 0
-
Trait: Wears glasses or contact lenses
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001925
Reference score
- Variants: 67,571
- Variants ignored: 0
-
Trait: Haematocrit percentage
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 67,571 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001926
Reference score
- Variants: 69,467
- Variants ignored: 0
-
Trait: Haemoglobin concentration
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 69,467 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001927
Reference score
- Variants: 73,846
- Variants ignored: 0
-
Trait: Hand grip strength (mean of both)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 73,846 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001928
Reference score
- Variants: 5,709
- Variants ignored: 0
-
Trait: Headaches for 3+ months
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 5,709 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001929
Reference score
- Variants: 156,514
- Variants ignored: 0
-
Trait: Standing height
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 156,514 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001930
Reference score
- Variants: 39,162
- Variants ignored: 0
-
Trait: Immature reticulocyte fraction
- Mapped Trait(s):
- EFO_0009253: Immature Reticulocyte Fraction Measurement
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 39,162 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001931
Reference score
- Variants: 41,836
- Variants ignored: 0
-
Trait: Average total household income before tax
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 41,836 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001932
Reference score
- Variants: 37,712
- Variants ignored: 0
-
Trait: Sleeplessness / insomnia
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 37,712 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001933
Reference score
- Variants: 25,604
- Variants ignored: 0
-
Trait: LDL direct
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 25,604 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001934
Reference score
- Variants: 50,955
- Variants ignored: 0
-
Trait: Alcohol intake frequency
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 50,955 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001935
Reference score
- Variants: 9,070
- Variants ignored: 0
-
Trait: General happiness with own health
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 9,070 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001936
Reference score
- Variants: 10,628
- Variants ignored: 0
-
Trait: General happiness
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 10,628 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001937
Reference score
- Variants: 16,197
- Variants ignored: 0
-
Trait: Ease of skin tanning
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 16,197 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001938
Reference score
- Variants: 64,164
- Variants ignored: 0
-
Trait: Age first had sexual intercourse
- Mapped Trait(s):
- EFO_0009749: age at first sexual intercourse measurement
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 64,164 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001939
Reference score
- Variants: 50,948
- Variants ignored: 0
-
Trait: Alkaline phosphatase
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 50,948 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001940
Reference score
- Variants: 51,849
- Variants ignored: 0
-
Trait: Alanine aminotransferase
- Mapped Trait(s):
- EFO_0004735: serum alanine aminotransferase measurement
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 51,849 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001941
Reference score
- Variants: 33,498
- Variants ignored: 0
-
Trait: Aspartate aminotransferase
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 33,498 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001942
Reference score
- Variants: 33,190
- Variants ignored: 0
-
Trait: Total bilirubin
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 33,190 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001943
Reference score
- Variants: 110,153
- Variants ignored: 0
-
Trait: Body mass index (BMI)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 110,153 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001944
Reference score
- Variants: 37,529
- Variants ignored: 0
-
Trait: Creatinine (enzymatic) in urine
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 37,529 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001945
Reference score
- Variants: 76,800
- Variants ignored: 0
-
Trait: Creatinine
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 76,800 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001946
Reference score
- Variants: 71,444
- Variants ignored: 0
-
Trait: C-reactive protein
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 71,444 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001947
Reference score
- Variants: 84,459
- Variants ignored: 0
-
Trait: Cystatin C
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 84,459 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001948
Reference score
- Variants: 1,967
- Variants ignored: 0
-
Trait: QRS duration
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 1,967 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001949
Reference score
- Variants: 9,236
- Variants ignored: 0
-
Trait: Eosinophil percentage
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 9,236 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001950
Reference score
- Variants: 128,827
- Variants ignored: 0
-
Trait: Whole body fat-free mass
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 128,827 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001951
Reference score
- Variants: 107,776
- Variants ignored: 0
-
Trait: Whole body fat mass
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 107,776 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001952
Reference score
- Variants: 14,811
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 14,811 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001953
Reference score
- Variants: 46,566
- Variants ignored: 0
-
Trait: Glycated haemoglobin (HbA1c)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 46,566 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001954
Reference score
- Variants: 85,429
- Variants ignored: 0
-
Trait: HDL cholesterol
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 85,429 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001955
Reference score
- Variants: 73,565
- Variants ignored: 0
-
Trait: Heel bone mineral density (BMD)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 73,565 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001956
Reference score
- Variants: 69,537
- Variants ignored: 0
-
Trait: Heel Broadband ultrasound attenuation, direct entry
- Mapped Trait(s):
- EFO_0007772: calcaneal bone quantitative ultrasound measurement
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 69,537 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001957
Reference score
- Variants: 65,064
- Variants ignored: 0
-
Trait: Speed of sound through heel
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 65,064 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001958
Reference score
- Variants: 103,123
- Variants ignored: 0
-
Trait: Hip circumference
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 103,123 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001959
Reference score
- Variants: 78,803
- Variants ignored: 0
-
Trait: High light scatter reticulocyte count
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 78,803 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001960
Reference score
- Variants: 87,149
- Variants ignored: 0
-
Trait: IGF-1
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 87,149 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001961
Reference score
- Variants: 119,500
- Variants ignored: 0
-
Trait: Impedance of whole body
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 119,500 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001962
Reference score
- Variants: 80,228
- Variants ignored: 0
-
Trait: White blood cell (leukocyte) count
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 80,228 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001963
Reference score
- Variants: 7,887
- Variants ignored: 0
-
Trait: Lipoprotein A
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 7,887 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001964
Reference score
- Variants: 76,069
- Variants ignored: 0
-
Trait: Gamma glutamyltransferase
- Mapped Trait(s):
- EFO_0004532: serum gamma-glutamyl transferase measurement
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 76,069 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001965
Reference score
- Variants: 76,535
- Variants ignored: 0
-
Trait: Lymphocyte count
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 76,535 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001966
Reference score
- Variants: 11,600
- Variants ignored: 0
-
Trait: Mean carotid IMT (intima-medial thickness) at 120/150/210/240 degrees
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 11,600 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001967
Reference score
- Variants: 948
- Variants ignored: 0
-
Trait: Microalbumin in urine
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 948 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001968
Reference score
- Variants: 46,673
- Variants ignored: 0
-
Trait: Monocyte count
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 46,673 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001969
Reference score
- Variants: 71,566
- Variants ignored: 0
-
Trait: Neutrophil count
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 71,566 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001970
Reference score
- Variants: 56,402
- Variants ignored: 0
-
Trait: Platelet crit
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 56,402 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001971
Reference score
- Variants: 65,450
- Variants ignored: 0
-
Trait: Mean platelet (thrombocyte) volume
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 65,450 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001972
Reference score
- Variants: 46,157
- Variants ignored: 0
-
Trait: Platelet distribution width
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 46,157 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001973
Reference score
- Variants: 60,665
- Variants ignored: 0
-
Trait: Platelet count
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 60,665 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001974
Reference score
- Variants: 21,512
- Variants ignored: 0
-
Trait: Potassium in urine
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 21,512 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001975
Reference score
- Variants: 62,254
- Variants ignored: 0
-
Trait: Pulse rate, automated reading
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 62,254 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001976
Reference score
- Variants: 75,033
- Variants ignored: 0
-
Trait: Reticulocyte count
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 75,033 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001977
Reference score
- Variants: 51,427
- Variants ignored: 0
-
Trait: Sex hormone binding globulin (SHBG)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 51,427 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001978
Reference score
- Variants: 40,037
- Variants ignored: 0
-
Trait: Sleep duration
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 40,037 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001979
Reference score
- Variants: 71,203
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 71,203 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001980
Reference score
- Variants: 56,782
- Variants ignored: 0
-
Trait: Urea
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 56,782 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001981
Reference score
- Variants: 6,324
- Variants ignored: 0
-
Trait: Ventricular rate
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 6,324 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001982
Reference score
- Variants: 35,123
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 35,123 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001983
Reference score
- Variants: 96,496
- Variants ignored: 0
-
Trait: Waist circumference
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 96,496 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001984
Reference score
- Variants: 127,910
- Variants ignored: 0
-
Trait: Whole body water mass
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 127,910 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001985
Reference score
- Variants: 223
- Variants ignored: 0
-
Trait: logMAR in round (left/right)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 223 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001986
Reference score
- Variants: 66,778
- Variants ignored: 0
-
Trait: Lymphocyte percentage
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 66,778 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001987
Reference score
- Variants: 23,692
- Variants ignored: 0
-
Trait: Hair/balding pattern
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 23,692 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001988
Reference score
- Variants: 3,985
- Variants ignored: 0
-
Trait: Testosterone (male only)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 3,985 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001989
Reference score
- Variants: 44,174
- Variants ignored: 0
-
Trait: Mean corpuscular haemoglobin
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 44,174 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001990
Reference score
- Variants: 47,916
- Variants ignored: 0
-
Trait: Mean corpuscular volume
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 47,916 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001991
Reference score
- Variants: 41,887
- Variants ignored: 0
-
Trait: Monocyte percentage
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 41,887 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001992
Reference score
- Variants: 61,542
- Variants ignored: 0
-
Trait: Morning/evening person (chronotype)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 61,542 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001993
Reference score
- Variants: 17,282
- Variants ignored: 0
-
Trait: Use of sun/uv protection
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 17,282 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001994
Reference score
- Variants: 30,217
- Variants ignored: 0
-
Trait: Myopia diagnosis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 30,217 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001995
Reference score
- Variants: 27,143
- Variants ignored: 0
-
Trait: Daytime dozing / sleeping (narcolepsy)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 27,143 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001996
Reference score
- Variants: 54,715
- Variants ignored: 0
-
Trait: Neuroticism score
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 54,715 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001997
Reference score
- Variants: 65,022
- Variants ignored: 0
-
Trait: Neutrophil percentage
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 65,022 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001998
Reference score
- Variants: 47,793
- Variants ignored: 0
-
Trait: Phosphate
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 47,793 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS001999
Reference score
- Variants: 50,215
- Variants ignored: 0
-
Trait: Plays computer games
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 50,215 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002000
Reference score
- Variants: 53,716
- Variants ignored: 0
-
Trait: Overall health rating
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 53,716 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002001
Reference score
- Variants: 69,557
- Variants ignored: 0
-
Trait: Total protein
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 69,557 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002002
Reference score
- Variants: 2,755
- Variants ignored: 0
-
Trait: Hair colour (natural, before greying)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 2,755 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002003
Reference score
- Variants: 24,536
- Variants ignored: 0
-
Trait: Mean reticulocyte volume
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 24,536 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002004
Reference score
- Variants: 3,970
- Variants ignored: 0
-
Trait: Sensitive stomach
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 3,970 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002005
Reference score
- Variants: 118,423
- Variants ignored: 0
-
Trait: Sitting height
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 118,423 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002006
Reference score
- Variants: 33,917
- Variants ignored: 0
-
Trait: Snoring
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 33,917 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002007
Reference score
- Variants: 37,568
- Variants ignored: 0
-
Trait: Sodium in urine
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 37,568 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002008
Reference score
- Variants: 50,360
- Variants ignored: 0
-
Trait: Mean sphered cell volume
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 50,360 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002009
Reference score
- Variants: 68,449
- Variants ignored: 0
-
Trait: Systolic blood pressure, automated reading
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 68,449 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002010
Reference score
- Variants: 75,102
- Variants ignored: 0
-
Trait: Urate
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 75,102 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002011
Reference score
- Variants: 43,709
- Variants ignored: 0
-
Trait: Water intake
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 43,709 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002012
Reference score
- Variants: 50,413
- Variants ignored: 0
-
Trait: Qualifications (years of education)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 50,413 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002013
Reference score
- Variants: 648,559
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 648,559 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002014
Reference score
- Variants: 534,399
- Variants ignored: 0
-
Trait: Skin cancer
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 534,399 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002015
Reference score
- Variants: 488,608
- Variants ignored: 0
-
Trait: Breast cancer [female]
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 488,608 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002016
Reference score
- Variants: 450,963
- Variants ignored: 0
-
Trait: Cancer of prostate
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 450,963 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002017
Reference score
- Variants: 510,453
- Variants ignored: 0
-
Trait: Cancer of bladder
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 510,453 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002018
Reference score
- Variants: 311,520
- Variants ignored: 0
-
Trait: Thyroid cancer
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 311,520 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002019
Reference score
- Variants: 667,546
- Variants ignored: 0
-
Trait: Benign neoplasm of colon
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 667,546 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002020
Reference score
- Variants: 503,832
- Variants ignored: 0
-
Trait: Benign neoplasm of other parts of digestive system
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 503,832 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002021
Reference score
- Variants: 547,617
- Variants ignored: 0
-
Trait: Benign neoplasm of uterus
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 547,617 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002022
Reference score
- Variants: 375,470
- Variants ignored: 0
-
Trait: Nontoxic multinodular goiter
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 375,470 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002023
Reference score
- Variants: 279,385
- Variants ignored: 0
-
Trait: Thyrotoxicosis with or without goiter
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 279,385 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002024
Reference score
- Variants: 632,597
- Variants ignored: 0
-
Trait: Hypothyroidism
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 632,597 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002025
Reference score
- Variants: 106,800
- Variants ignored: 0
-
Trait: Type 1 diabetes
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 106,800 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002026
Reference score
- Variants: 830,783
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 830,783 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002027
Reference score
- Variants: 389,029
- Variants ignored: 0
-
Trait: Diabetic retinopathy
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 389,029 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002028
Reference score
- Variants: 170,554
- Variants ignored: 0
-
Trait: Hypoglycemia
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 170,554 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002029
Reference score
- Variants: 764,390
- Variants ignored: 0
-
Trait: Disorders of lipoid metabolism
- Mapped Trait(s):
- HP_0003119: Abnormal circulating lipid concentration
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 764,390 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002030
Reference score
- Variants: 163,210
- Variants ignored: 0
-
Trait: Gout
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 163,210 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002031
Reference score
- Variants: 6,713
- Variants ignored: 0
-
Trait: Disorders of iron metabolism
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 6,713 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002032
Reference score
- Variants: 19,768
- Variants ignored: 0
-
Trait: Disorders of bilirubin excretion
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 19,768 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002033
Reference score
- Variants: 846,292
- Variants ignored: 0
-
Trait: Overweight, obesity and other hyperalimentation
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 846,292 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002034
Reference score
- Variants: 32,552
- Variants ignored: 0
-
Trait: Congenital deficiency of other clotting factors (including factor VII)
- Mapped Trait(s):
- MONDO_0015722: congenital vitamin K-dependent coagulation factors deficiency
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 32,552 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002035
Reference score
- Variants: 39,752
- Variants ignored: 0
-
Trait: Dementias
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 39,752 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002036
Reference score
- Variants: 807,338
- Variants ignored: 0
-
Trait: Depression
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 807,338 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002037
Reference score
- Variants: 847,691
- Variants ignored: 0
-
Trait: Tobacco use disorder
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 847,691 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002038
Reference score
- Variants: 129,077
- Variants ignored: 0
-
Trait: Multiple sclerosis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 129,077 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002039
Reference score
- Variants: 799,326
- Variants ignored: 0
-
Trait: Other peripheral nerve disorders
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 799,326 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002040
Reference score
- Variants: 706,872
- Variants ignored: 0
-
Trait: Retinal detachments and defects
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 706,872 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002041
Reference score
- Variants: 116,538
- Variants ignored: 0
-
Trait: Macular degeneration (senile) of retina NOS
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 116,538 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002042
Reference score
- Variants: 59,944
- Variants ignored: 0
-
Trait: Corneal dystrophy
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 59,944 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002043
Reference score
- Variants: 672,952
- Variants ignored: 0
-
Trait: Glaucoma
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 672,952 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002044
Reference score
- Variants: 711,169
- Variants ignored: 0
-
Trait: Cataract
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 711,169 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002045
Reference score
- Variants: 527,030
- Variants ignored: 0
-
Trait: Inflammation of the eye
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 527,030 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002046
Reference score
- Variants: 570,308
- Variants ignored: 0
-
Trait: Otosclerosis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 570,308 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002047
Reference score
- Variants: 918,325
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 918,325 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002048
Reference score
- Variants: 762,124
- Variants ignored: 0
-
Trait: Coronary atherosclerosis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 762,124 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002049
Reference score
- Variants: 222,371
- Variants ignored: 0
-
Trait: Pulmonary heart disease
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 222,371 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002050
Reference score
- Variants: 554,908
- Variants ignored: 0
-
Trait: Atrial fibrillation and flutter
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 554,908 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002051
Reference score
- Variants: 642,241
- Variants ignored: 0
-
Trait: Congestive heart failure; nonhypertensive
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 642,241 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002052
Reference score
- Variants: 490,459
- Variants ignored: 0
-
Trait: Occlusion and stenosis of precerebral arteries
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 490,459 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002053
Reference score
- Variants: 599,726
- Variants ignored: 0
-
Trait: Cerebrovascular disease
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 599,726 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002054
Reference score
- Variants: 592,187
- Variants ignored: 0
-
Trait: Abdominal aortic aneurysm
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 592,187 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002055
Reference score
- Variants: 599,514
- Variants ignored: 0
-
Trait: Peripheral vascular disease, unspecified
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 599,514 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002056
Reference score
- Variants: 114,679
- Variants ignored: 0
-
Trait: Phlebitis and thrombophlebitis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 114,679 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002057
Reference score
- Variants: 760,630
- Variants ignored: 0
-
Trait: Varicose veins
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 760,630 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002058
Reference score
- Variants: 780,418
- Variants ignored: 0
-
Trait: Hemorrhoids
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 780,418 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002059
Reference score
- Variants: 604,572
- Variants ignored: 0
-
Trait: Circulatory disease NEC
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 604,572 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002060
Reference score
- Variants: 553,242
- Variants ignored: 0
-
Trait: Nasal polyps
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 553,242 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002061
Reference score
- Variants: 793,375
- Variants ignored: 0
-
Trait: Asthma
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 793,375 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002062
Reference score
- Variants: 811,003
- Variants ignored: 0
-
Trait: Chronic airway obstruction
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 811,003 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002063
Reference score
- Variants: 836,413
- Variants ignored: 0
-
Trait: Esophagitis, GERD and related diseases
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 836,413 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002064
Reference score
- Variants: 497,422
- Variants ignored: 0
-
Trait: Appendiceal conditions
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 497,422 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002065
Reference score
- Variants: 691,268
- Variants ignored: 0
-
Trait: Inguinal hernia
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 691,268 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002066
Reference score
- Variants: 566,637
- Variants ignored: 0
-
Trait: Ulcerative colitis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 566,637 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002067
Reference score
- Variants: 58,231
- Variants ignored: 0
-
Trait: Celiac disease
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 58,231 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002068
Reference score
- Variants: 831,212
- Variants ignored: 0
-
Trait: Diverticulosis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 831,212 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002069
Reference score
- Variants: 747,820
- Variants ignored: 0
-
Trait: Functional digestive disorders
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 747,820 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002070
Reference score
- Variants: 584,133
- Variants ignored: 0
-
Trait: Anal and rectal polyp
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 584,133 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002071
Reference score
- Variants: 352,506
- Variants ignored: 0
-
Trait: Other chronic nonalcoholic liver disease
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 352,506 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002072
Reference score
- Variants: 428,587
- Variants ignored: 0
-
Trait: Cholelithiasis and cholecystitis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 428,587 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002073
Reference score
- Variants: 363,801
- Variants ignored: 0
-
Trait: Other biliary tract disease
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 363,801 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002074
Reference score
- Variants: 664,167
- Variants ignored: 0
-
Trait: Hematuria
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 664,167 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002075
Reference score
- Variants: 731,196
- Variants ignored: 0
-
Trait: Urinary calculus
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 731,196 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002076
Reference score
- Variants: 627,341
- Variants ignored: 0
-
Trait: Hyperplasia of prostate
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 627,341 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002077
Reference score
- Variants: 534,802
- Variants ignored: 0
-
Trait: Endometriosis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 534,802 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002078
Reference score
- Variants: 774,553
- Variants ignored: 0
-
Trait: Genital prolapse
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 774,553 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002079
Reference score
- Variants: 719,789
- Variants ignored: 0
-
Trait: Irregular menstrual cycle/bleeding
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 719,789 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002080
Reference score
- Variants: 32,414
- Variants ignored: 0
-
Trait: Rhesus isoimmunization in pregnancy
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 32,414 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002081
Reference score
- Variants: 640,921
- Variants ignored: 0
-
Trait: Superficial cellulitis and abscess
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 640,921 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002082
Reference score
- Variants: 361,553
- Variants ignored: 0
-
Trait: Lupus (localized and systemic)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 361,553 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002083
Reference score
- Variants: 71,744
- Variants ignored: 0
-
Trait: Psoriasis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 71,744 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002084
Reference score
- Variants: 403,417
- Variants ignored: 0
-
Trait: Sarcoidosis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 403,417 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002085
Reference score
- Variants: 481,233
- Variants ignored: 0
-
Trait: Seborrheic keratosis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 481,233 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002086
Reference score
- Variants: 160,693
- Variants ignored: 0
-
Trait: Diseases of hair and hair follicles
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 160,693 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002087
Reference score
- Variants: 206,669
- Variants ignored: 0
-
Trait: Sebaceous cyst
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 206,669 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002088
Reference score
- Variants: 95,083
- Variants ignored: 0
-
Trait: Rheumatoid arthritis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 95,083 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002089
Reference score
- Variants: 22,026
- Variants ignored: 0
-
Trait: Ankylosing spondylitis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 22,026 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002090
Reference score
- Variants: 859,336
- Variants ignored: 0
-
Trait: Other arthropathies
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 859,336 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002091
Reference score
- Variants: 129,938
- Variants ignored: 0
-
Trait: Polymyalgia Rheumatica
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 129,938 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002092
Reference score
- Variants: 484,484
- Variants ignored: 0
-
Trait: Contracture of palmar fascia [Dupuytren's disease]
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 484,484 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002093
Reference score
- Variants: 773,461
- Variants ignored: 0
-
Trait: Hallux valgus (Bunion)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 773,461 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002094
Reference score
- Variants: 827,887
- Variants ignored: 0
-
Trait: Osteoarthrosis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 827,887 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002095
Reference score
- Variants: 658,775
- Variants ignored: 0
-
Trait: Osteoporosis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 658,775 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002096
Reference score
- Variants: 791,954
- Variants ignored: 0
-
Trait: Abdominal pain
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 791,954 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002097
Reference score
- Variants: 742,904
- Variants ignored: 0
-
Trait: Allergy/adverse effect of penicillin
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 742,904 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002098
Reference score
- Variants: 764,146
- Variants ignored: 0
-
Trait: Recent poor appetite or overeating
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 764,146 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002099
Reference score
- Variants: 816,264
- Variants ignored: 0
-
Trait: Albumin
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 816,264 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002100
Reference score
- Variants: 917,925
- Variants ignored: 0
-
Trait: Ankle spacing width
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 917,925 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002101
Reference score
- Variants: 681,234
- Variants ignored: 0
-
Trait: Apolipoprotein A
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 681,234 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002102
Reference score
- Variants: 315,483
- Variants ignored: 0
-
Trait: Apolipoprotein B
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 315,483 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002103
Reference score
- Variants: 833,170
- Variants ignored: 0
-
Trait: avMSE
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 833,170 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002104
Reference score
- Variants: 869,179
- Variants ignored: 0
-
Trait: Hearing difficulty/problems
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 869,179 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002105
Reference score
- Variants: 827,714
- Variants ignored: 0
-
Trait: Birth weight
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 827,714 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002106
Reference score
- Variants: 702,009
- Variants ignored: 0
-
Trait: Calcium
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 702,009 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002107
Reference score
- Variants: 39,066
- Variants ignored: 0
-
Trait: Diagnosed with coeliac disease or gluten sensitivity
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 39,066 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002108
Reference score
- Variants: 451,160
- Variants ignored: 0
-
Trait: Cholesterol
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 451,160 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002109
Reference score
- Variants: 393,500
- Variants ignored: 0
-
Trait: Hair colour (natural, before greying)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 393,500 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002110
Reference score
- Variants: 275,831
- Variants ignored: 0
-
Trait: Skin colour
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 275,831 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002111
Reference score
- Variants: 791,873
- Variants ignored: 0
-
Trait: Ever depressed for a whole week
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 791,873 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002112
Reference score
- Variants: 748,601
- Variants ignored: 0
-
Trait: Recent feelings of depression
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 748,601 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002113
Reference score
- Variants: 545,334
- Variants ignored: 0
-
Trait: Depression possibly related to stressful or traumatic event
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 545,334 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002114
Reference score
- Variants: 933,950
- Variants ignored: 0
-
Trait: Diastolic blood pressure, automated reading
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 933,950 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002115
Reference score
- Variants: 766,714
- Variants ignored: 0
-
Trait: Alcohol drinker status
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 766,714 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002116
Reference score
- Variants: 564,874
- Variants ignored: 0
-
Trait: P duration
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 564,874 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002117
Reference score
- Variants: 667,705
- Variants ignored: 0
-
Trait: PP interval
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 667,705 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002118
Reference score
- Variants: 413,539
- Variants ignored: 0
-
Trait: PQ interval
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 413,539 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002119
Reference score
- Variants: 571,268
- Variants ignored: 0
-
Trait: QT interval
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 571,268 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002120
Reference score
- Variants: 490,392
- Variants ignored: 0
-
Trait: QTC interval
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 490,392 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002121
Reference score
- Variants: 616,710
- Variants ignored: 0
-
Trait: RR interval
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 616,710 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002122
Reference score
- Variants: 543,714
- Variants ignored: 0
-
Trait: Red blood cell (erythrocyte) distribution width
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 543,714 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002123
Reference score
- Variants: 788,123
- Variants ignored: 0
-
Trait: Red blood cell (erythrocyte) count
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 788,123 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002124
Reference score
- Variants: 566,292
- Variants ignored: 0
-
Trait: Ever addicted to any substance or behaviour
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 566,292 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002125
Reference score
- Variants: 816,604
- Variants ignored: 0
-
Trait: Ever taken cannabis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 816,604 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002126
Reference score
- Variants: 931,635
- Variants ignored: 0
-
Trait: Ever smoked
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 931,635 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002127
Reference score
- Variants: 848,784
- Variants ignored: 0
-
Trait: Age at first live birth
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 848,784 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002128
Reference score
- Variants: 414,081
- Variants ignored: 0
-
Trait: Length of menstrual cycle
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 414,081 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002129
Reference score
- Variants: 491,888
- Variants ignored: 0
-
Trait: Length of menstrual cycle
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 491,888 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002130
Reference score
- Variants: 650,195
- Variants ignored: 0
-
Trait: Testosterone (female only)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 650,195 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002131
Reference score
- Variants: 854,735
- Variants ignored: 0
-
Trait: Age when periods started (menarche)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 854,735 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002132
Reference score
- Variants: 826,502
- Variants ignored: 0
-
Trait: Falls in the last year
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 826,502 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002133
Reference score
- Variants: 995,419
- Variants ignored: 0
-
Trait: Body fat percentage
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 995,419 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002134
Reference score
- Variants: 940,003
- Variants ignored: 0
-
Trait: Forced expiratory volume in 1-second (FEV1), Best measure
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 940,003 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002135
Reference score
- Variants: 903,259
- Variants ignored: 0
-
Trait: Fluid intelligence score
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 903,259 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002136
Reference score
- Variants: 733,839
- Variants ignored: 0
-
Trait: Recent feelings of foreboding
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 733,839 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002137
Reference score
- Variants: 738,021
- Variants ignored: 0
-
Trait: Fractured/broken bones in last 5 years
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 738,021 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002138
Reference score
- Variants: 940,300
- Variants ignored: 0
-
Trait: Forced vital capacity (FVC), Best measure
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 940,300 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002139
Reference score
- Variants: 956,532
- Variants ignored: 0
-
Trait: Time spent watching television (TV) or using computer
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 956,532 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002140
Reference score
- Variants: 762,684
- Variants ignored: 0
-
Trait: Wears glasses or contact lenses
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 762,684 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002141
Reference score
- Variants: 797,804
- Variants ignored: 0
-
Trait: Haematocrit percentage
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 797,804 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002142
Reference score
- Variants: 786,386
- Variants ignored: 0
-
Trait: Haemoglobin concentration
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 786,386 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002143
Reference score
- Variants: 966,283
- Variants ignored: 0
-
Trait: Hand grip strength (mean of both)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 966,283 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002144
Reference score
- Variants: 539,784
- Variants ignored: 0
-
Trait: Trouble falling asleep
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 539,784 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002145
Reference score
- Variants: 720,580
- Variants ignored: 0
-
Trait: Headaches for 3+ months
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 720,580 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002146
Reference score
- Variants: 922,538
- Variants ignored: 0
-
Trait: Standing height
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 922,538 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002147
Reference score
- Variants: 664,696
- Variants ignored: 0
-
Trait: Immature reticulocyte fraction
- Mapped Trait(s):
- EFO_0009253: Immature Reticulocyte Fraction Measurement
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 664,696 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002148
Reference score
- Variants: 932,197
- Variants ignored: 0
-
Trait: Average total household income before tax
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 932,197 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002149
Reference score
- Variants: 926,585
- Variants ignored: 0
-
Trait: Sleeplessness / insomnia
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 926,585 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002150
Reference score
- Variants: 360,007
- Variants ignored: 0
-
Trait: LDL direct
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 360,007 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002151
Reference score
- Variants: 734,236
- Variants ignored: 0
-
Trait: Handedness (chirality/laterality)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 734,236 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002152
Reference score
- Variants: 946,965
- Variants ignored: 0
-
Trait: Alcohol intake frequency
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 946,965 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002153
Reference score
- Variants: 824,602
- Variants ignored: 0
-
Trait: General happiness with own health
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 824,602 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002154
Reference score
- Variants: 806,011
- Variants ignored: 0
-
Trait: General happiness
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 806,011 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002155
Reference score
- Variants: 240,701
- Variants ignored: 0
-
Trait: Ease of skin tanning
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 240,701 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002156
Reference score
- Variants: 972,919
- Variants ignored: 0
-
Trait: Age first had sexual intercourse
- Mapped Trait(s):
- EFO_0009749: age at first sexual intercourse measurement
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 972,919 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002157
Reference score
- Variants: 874,365
- Variants ignored: 0
-
Trait: Alkaline phosphatase
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 874,365 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002158
Reference score
- Variants: 774,274
- Variants ignored: 0
-
Trait: Alanine aminotransferase
- Mapped Trait(s):
- EFO_0004735: serum alanine aminotransferase measurement
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 774,274 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002159
Reference score
- Variants: 716,914
- Variants ignored: 0
-
Trait: Aspartate aminotransferase
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 716,914 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002160
Reference score
- Variants: 120,068
- Variants ignored: 0
-
Trait: Total bilirubin
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 120,068 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002161
Reference score
- Variants: 990,022
- Variants ignored: 0
-
Trait: Body mass index (BMI)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 990,022 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002162
Reference score
- Variants: 922,786
- Variants ignored: 0
-
Trait: Creatinine (enzymatic) in urine
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 922,786 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002163
Reference score
- Variants: 835,964
- Variants ignored: 0
-
Trait: Creatinine
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 835,964 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002164
Reference score
- Variants: 736,345
- Variants ignored: 0
-
Trait: C-reactive protein
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 736,345 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002165
Reference score
- Variants: 781,302
- Variants ignored: 0
-
Trait: Cystatin C
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 781,302 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002166
Reference score
- Variants: 471,172
- Variants ignored: 0
-
Trait: QRS duration
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 471,172 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002167
Reference score
- Variants: 593,459
- Variants ignored: 0
-
Trait: Eosinophil percentage
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 593,459 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002168
Reference score
- Variants: 966,825
- Variants ignored: 0
-
Trait: Whole body fat-free mass
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 966,825 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002169
Reference score
- Variants: 988,292
- Variants ignored: 0
-
Trait: Whole body fat mass
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 988,292 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002170
Reference score
- Variants: 602,241
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 602,241 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002171
Reference score
- Variants: 736,730
- Variants ignored: 0
-
Trait: Glycated haemoglobin (HbA1c)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 736,730 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002172
Reference score
- Variants: 732,902
- Variants ignored: 0
-
Trait: HDL cholesterol
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 732,902 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002173
Reference score
- Variants: 729,074
- Variants ignored: 0
-
Trait: Heel bone mineral density (BMD)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 729,074 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002174
Reference score
- Variants: 732,595
- Variants ignored: 0
-
Trait: Heel Broadband ultrasound attenuation, direct entry
- Mapped Trait(s):
- EFO_0007772: calcaneal bone quantitative ultrasound measurement
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 732,595 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002175
Reference score
- Variants: 724,667
- Variants ignored: 0
-
Trait: Speed of sound through heel
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 724,667 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002176
Reference score
- Variants: 977,411
- Variants ignored: 0
-
Trait: Hip circumference
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 977,411 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002177
Reference score
- Variants: 780,048
- Variants ignored: 0
-
Trait: High light scatter reticulocyte count
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 780,048 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002178
Reference score
- Variants: 817,740
- Variants ignored: 0
-
Trait: IGF-1
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 817,740 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002179
Reference score
- Variants: 978,109
- Variants ignored: 0
-
Trait: Impedance of whole body
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 978,109 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002180
Reference score
- Variants: 846,337
- Variants ignored: 0
-
Trait: White blood cell (leukocyte) count
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 846,337 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002181
Reference score
- Variants: 31,355
- Variants ignored: 0
-
Trait: Lipoprotein A
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 31,355 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002182
Reference score
- Variants: 713,481
- Variants ignored: 0
-
Trait: Gamma glutamyltransferase
- Mapped Trait(s):
- EFO_0004532: serum gamma-glutamyl transferase measurement
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 713,481 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002183
Reference score
- Variants: 814,921
- Variants ignored: 0
-
Trait: Lymphocyte count
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 814,921 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002184
Reference score
- Variants: 734,561
- Variants ignored: 0
-
Trait: Mean carotid IMT (intima-medial thickness) at 120/150/210/240 degrees
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 734,561 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002185
Reference score
- Variants: 671,610
- Variants ignored: 0
-
Trait: Microalbumin in urine
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 671,610 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002186
Reference score
- Variants: 641,455
- Variants ignored: 0
-
Trait: Monocyte count
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 641,455 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002187
Reference score
- Variants: 803,767
- Variants ignored: 0
-
Trait: Neutrophil count
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 803,767 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002188
Reference score
- Variants: 703,576
- Variants ignored: 0
-
Trait: Platelet crit
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 703,576 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002189
Reference score
- Variants: 462,934
- Variants ignored: 0
-
Trait: Mean platelet (thrombocyte) volume
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 462,934 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002190
Reference score
- Variants: 482,649
- Variants ignored: 0
-
Trait: Platelet distribution width
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 482,649 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002191
Reference score
- Variants: 663,591
- Variants ignored: 0
-
Trait: Platelet count
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 663,591 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002192
Reference score
- Variants: 881,567
- Variants ignored: 0
-
Trait: Potassium in urine
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 881,567 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002193
Reference score
- Variants: 858,487
- Variants ignored: 0
-
Trait: Pulse rate, automated reading
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 858,487 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002194
Reference score
- Variants: 773,305
- Variants ignored: 0
-
Trait: Reticulocyte count
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 773,305 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002195
Reference score
- Variants: 650,364
- Variants ignored: 0
-
Trait: Sex hormone binding globulin (SHBG)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 650,364 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002196
Reference score
- Variants: 927,619
- Variants ignored: 0
-
Trait: Sleep duration
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 927,619 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002197
Reference score
- Variants: 731,035
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 731,035 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002198
Reference score
- Variants: 820,118
- Variants ignored: 0
-
Trait: Urea
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 820,118 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002199
Reference score
- Variants: 705,680
- Variants ignored: 0
-
Trait: Ventricular rate
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 705,680 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002200
Reference score
- Variants: 567,735
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 567,735 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002201
Reference score
- Variants: 984,035
- Variants ignored: 0
-
Trait: Waist circumference
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 984,035 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002202
Reference score
- Variants: 966,737
- Variants ignored: 0
-
Trait: Whole body water mass
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 966,737 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002203
Reference score
- Variants: 775,312
- Variants ignored: 0
-
Trait: Lymphocyte percentage
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 775,312 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002204
Reference score
- Variants: 593,179
- Variants ignored: 0
-
Trait: Hair/balding pattern
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 593,179 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002205
Reference score
- Variants: 584,991
- Variants ignored: 0
-
Trait: Testosterone (male only)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 584,991 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002206
Reference score
- Variants: 504,929
- Variants ignored: 0
-
Trait: Mean corpuscular haemoglobin
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 504,929 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002207
Reference score
- Variants: 564,228
- Variants ignored: 0
-
Trait: Mean corpuscular volume
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 564,228 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002208
Reference score
- Variants: 544,905
- Variants ignored: 0
-
Trait: Monocyte percentage
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 544,905 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002209
Reference score
- Variants: 955,439
- Variants ignored: 0
-
Trait: Morning/evening person (chronotype)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 955,439 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002210
Reference score
- Variants: 821,654
- Variants ignored: 0
-
Trait: Use of sun/uv protection
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 821,654 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002211
Reference score
- Variants: 825,631
- Variants ignored: 0
-
Trait: Myopia diagnosis
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 825,631 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002212
Reference score
- Variants: 893,802
- Variants ignored: 0
-
Trait: Daytime dozing / sleeping (narcolepsy)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 893,802 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002213
Reference score
- Variants: 950,183
- Variants ignored: 0
-
Trait: Neuroticism score
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 950,183 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002214
Reference score
- Variants: 769,542
- Variants ignored: 0
-
Trait: Neutrophil percentage
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 769,542 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002215
Reference score
- Variants: 633,660
- Variants ignored: 0
-
Trait: Age first had sexual intercourse
- Mapped Trait(s):
- EFO_0009749: age at first sexual intercourse measurement
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 633,660 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002216
Reference score
- Variants: 708,693
- Variants ignored: 0
-
Trait: Phosphate
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 708,693 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002217
Reference score
- Variants: 938,047
- Variants ignored: 0
-
Trait: Plays computer games
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 938,047 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002218
Reference score
- Variants: 958,362
- Variants ignored: 0
-
Trait: Overall health rating
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 958,362 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002219
Reference score
- Variants: 819,013
- Variants ignored: 0
-
Trait: Total protein
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 819,013 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002220
Reference score
- Variants: 21,400
- Variants ignored: 0
-
Trait: Hair colour (natural, before greying)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 21,400 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002221
Reference score
- Variants: 523,074
- Variants ignored: 0
-
Trait: Mean reticulocyte volume
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 523,074 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002222
Reference score
- Variants: 761,279
- Variants ignored: 0
-
Trait: Ever contemplated self-harm / Recent thoughts of suicide or self-harm
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 761,279 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002223
Reference score
- Variants: 795,614
- Variants ignored: 0
-
Trait: Sensitive stomach
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 795,614 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002224
Reference score
- Variants: 910,252
- Variants ignored: 0
-
Trait: Sitting height
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 910,252 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002225
Reference score
- Variants: 913,306
- Variants ignored: 0
-
Trait: Snoring
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 913,306 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002226
Reference score
- Variants: 922,972
- Variants ignored: 0
-
Trait: Sodium in urine
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 922,972 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002227
Reference score
- Variants: 630,576
- Variants ignored: 0
-
Trait: Mean sphered cell volume
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 630,576 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002228
Reference score
- Variants: 937,030
- Variants ignored: 0
-
Trait: Systolic blood pressure, automated reading
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 937,030 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002229
Reference score
- Variants: 698,001
- Variants ignored: 0
-
Trait: Urate
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 698,001 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002230
Reference score
- Variants: 930,461
- Variants ignored: 0
-
Trait: Water intake
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 930,461 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002231
Reference score
- Variants: 950,845
- Variants ignored: 0
-
Trait: Qualifications (years of education)
- Mapped Trait(s):
- Publication: Privé F et.al, Am J Hum Genet (2022-01-06)
- View in PGS-Catalog
Target study
- Coverage: 950,845 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002232
Reference score
- Variants: 263,279
- Variants ignored: 0
-
Trait: Stool Frequency
- Mapped Trait(s):
- Samples: 167,875
- Population:
- Publication: Bonfiglio F et.al, Cell Genom (2021-12-08)
- View in PGS-Catalog
Target study
- Coverage: 262,707 (99.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002233
Reference score
- Variants: 27
- Variants ignored: 0
-
Trait: Nicotine metabolite ratio
- Mapped Trait(s):
- Samples: 1,518
- Population:
- Publication: Chen LS et.al, Pharmacogenomics (2018-11-16)
- View in PGS-Catalog
Target study
- Coverage: 27 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002234
Reference score
- Variants: 10
- Variants ignored: 0
-
Trait: Nicotine metabolite ratio
- Mapped Trait(s):
- Samples: 212
- Population:
- Publication: Chen LS et.al, Pharmacogenomics (2018-11-16)
- View in PGS-Catalog
Target study
- Coverage: 10 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002235
Reference score
- Variants: 36
- Variants ignored: 6
-
Trait: Venous thromboembolism
- Mapped Trait(s):
- Samples: 1,020,612
- Population:
- European: 92.4%
- African: 5.1%
- Hispanic or Latin American: 2.1%
- Multi-Ancestry (including Europeans): 0.4%
- Publication: Kolin DA et.al, Sci Rep (2021-11-01)
- View in PGS-Catalog
Target study
- Coverage: 27 (75%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002236
Reference score
- Variants: 92,299
- Variants ignored: 0
-
Trait: Ascending aorta diameter (MRI-derived)
- Mapped Trait(s):
- Samples: 20,642
- Population:
- Publication: Tcheandjieu C et.al, Nat Genet (2022-05-30)
- View in PGS-Catalog
Target study
- Coverage: 65,485 (70.95%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002237
Reference score
- Variants: 471,316
- Variants ignored: 0
-
Trait: Chronic Kidney Disease (stage 3 or greater)
- Mapped Trait(s):
- Publication: Khan A et.al, Nat Med (2022-06-16)
- View in PGS-Catalog
Target study
- Coverage: 471,316 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002238
Reference score
- Variants: 1,119,444
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 627,529
- Population:
- European: 58.3%
- East Asian: 21.8%
- African: 15.1%
- Hispanic or Latin American: 3.6%
- Additional Asian Ancestries: 0.8%
- Additional Diverse Ancestries: 0.4%
- Publication: Breeyear JH et.al, Circ Genom Precis Med (2022-05-06)
- View in PGS-Catalog
Target study
- Coverage: 1,119,444 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002239
Reference score
- Variants: 1,119,054
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 627,547
- Population:
- European: 58.3%
- East Asian: 21.8%
- African: 15.1%
- Hispanic or Latin American: 3.6%
- Additional Asian Ancestries: 0.8%
- Additional Diverse Ancestries: 0.4%
- Publication: Breeyear JH et.al, Circ Genom Precis Med (2022-05-06)
- View in PGS-Catalog
Target study
- Coverage: 1,119,054 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002240
Reference score
- Variants: 1,092,093
- Variants ignored: 0
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 140,254
- Population:
- Publication: Mars N et.al, Cell Genom (2022-04-13)
- View in PGS-Catalog
Target study
- Coverage: 1,091,736 (99.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002241
Reference score
- Variants: 6,497,734
- Variants ignored: 0
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 140,254
- Population:
- Publication: Mars N et.al, Cell Genom (2022-04-13)
- View in PGS-Catalog
Target study
- Coverage: 6,497,734 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002242
Reference score
- Variants: 6,494,889
- Variants ignored: 0
-
Trait: Breast cancer
- Mapped Trait(s):
- Samples: 139,274
- Population:
- Publication: Mars N et.al, Cell Genom (2022-04-13)
- View in PGS-Catalog
Target study
- Coverage: 6,494,889 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002243
Reference score
- Variants: 6,431,973
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 159,208
- Population:
- Publication: Mars N et.al, Cell Genom (2022-04-13)
- View in PGS-Catalog
Target study
- Coverage: 6,431,973 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002244
Reference score
- Variants: 6,576,338
- Variants ignored: 0
-
Trait: Coronary artery disease
- Mapped Trait(s):
- Samples: 187,599
- Population:
- European: 75.3%
- South Asian: 13.6%
- East Asian: 6%
- Hispanic or Latin American: 2.2%
- African: 1.7%
- Greater Middle Eastern: 1.2%
- Publication: Mars N et.al, Cell Genom (2022-04-13)
- View in PGS-Catalog
Target study
- Coverage: 6,576,338 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002245
Reference score
- Variants: 8
- Variants ignored: 0
-
Trait: Liver fat (MRI-derived)
- Mapped Trait(s):
- Samples: 32,974
- Population:
- Publication: Haas ME et.al, Cell Genom (2021-12-01)
- View in PGS-Catalog
Target study
- Coverage: 8 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002246
Reference score
- Variants: 50
- Variants ignored: 0
-
Trait: Melanoma
- Mapped Trait(s):
- Samples: 385,443
- Population:
- Publication: Steinberg J et.al, Br J Dermatol (2021-12-18)
- View in PGS-Catalog
Target study
- Coverage: 50 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002247
Reference score
- Variants: 68
- Variants ignored: 0
-
Trait: Melanoma
- Mapped Trait(s):
- Samples: 411,948
- Population:
- Publication: Steinberg J et.al, Br J Dermatol (2021-12-18)
- View in PGS-Catalog
Target study
- Coverage: 68 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002248
Reference score
- Variants: 105
- Variants ignored: 41
-
Trait: Childhood asthma
- Mapped Trait(s):
- Samples: 314,633
- Population:
- Publication: Kothalawala DM et.al, J Pers Med (2022-01-08)
- View in PGS-Catalog
Target study
- Coverage: 64 (60.95%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002249
Reference score
- Variants: 249,273
- Variants ignored: 23,236
-
Trait: Alzheimer disease
- Mapped Trait(s):
- Samples: 55,134
- Population:
- Publication: Lourida I et.al, JAMA (2019-08-01)
- View in PGS-Catalog
Target study
- Coverage: 224,796 (90.18%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002250
Reference score
- Variants: 27,240
- Variants ignored: 0
-
Trait: Epithelial ovarian cancer
- Mapped Trait(s):
- Publication: Dareng EO et.al, Eur J Hum Genet (2022-01-14)
- View in PGS-Catalog
Target study
- Coverage: 26,571 (97.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002251
Reference score
- Variants: 97
- Variants ignored: 0
-
Trait: Body mass index
- Mapped Trait(s):
- Samples: 238,944
- Population:
- European: 99.1%
- Hispanic or Latin American: 0.5%
- African: 0.4%
- Publication: Dashti HS et.al, BMC Med (2022-01-12)
- View in PGS-Catalog
Target study
- Coverage: 95 (97.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002252
Reference score
- Variants: 141
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 658,218
- Population:
- European: 80.5%
- East Asian: 18.5%
- African: 1%
- Publication: Archambault AN et.al, J Natl Cancer Inst (2022-01-13)
- View in PGS-Catalog
Target study
- Coverage: 130 (92.2%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002253
Reference score
- Variants: 45
- Variants ignored: 0
-
Trait: Melanoma
- Mapped Trait(s):
- Samples: 42,399
- Population:
- Publication: Steinberg J et.al, Br J Dermatol (2021-12-18)
- View in PGS-Catalog
Target study
- Coverage: 44 (97.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002254
Reference score
- Variants: 1,142,416
- Variants ignored: 0
-
Trait: Physical activity (self-reported)
- Mapped Trait(s):
- Samples: 321,309
- Population:
- Publication: Kujala UM et.al, Med Sci Sports Exerc (2020-07-01)
- View in PGS-Catalog
Target study
- Coverage: 1,139,818 (99.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002255
Reference score
- Variants: 1,140,182
- Variants ignored: 480,321
-
Trait: Physical activity (measured)
- Mapped Trait(s):
- Samples: 91,105
- Population:
- Publication: Kujala UM et.al, Med Sci Sports Exerc (2020-07-01)
- View in PGS-Catalog
Target study
- Coverage: 658,830 (57.78%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002256
Reference score
- Variants: 4
- Variants ignored: 0
-
Trait: Gestational diabetes mellitus in early pregnancy
- Mapped Trait(s):
- Samples: 671
- Population:
- Publication: Wu Q et.al, Diabetol Metab Syndr (2022-01-24)
- View in PGS-Catalog
Target study
- Coverage: 4 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002257
Reference score
- Variants: 884
- Variants ignored: 0
-
Trait: Systolic blood pressure
- Mapped Trait(s):
- Samples: 757,601
- Population:
- Publication: Evangelou E et.al, Nat Genet (2018-09-17)
- View in PGS-Catalog
Target study
- Coverage: 879 (99.43%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002258
Reference score
- Variants: 885
- Variants ignored: 0
-
Trait: Diastolic blood pressure
- Mapped Trait(s):
- Samples: 757,601
- Population:
- Publication: Evangelou E et.al, Nat Genet (2018-09-17)
- View in PGS-Catalog
Target study
- Coverage: 880 (99.44%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002259
Reference score
- Variants: 534
- Variants ignored: 0
-
Trait: Stroke
- Mapped Trait(s):
- Samples: 2,442,550
- Population:
- European: 47%
- Unknown: 30.4%
- East Asian: 14.6%
- South Asian: 3%
- Multi-Ancestry (including Europeans): 2.6%
- African: 1.6%
- Hispanic or Latin American: 0.3%
- Multi-Ancestry (excluding Europeans): 0.2%
- Additional Asian Ancestries: 0.2%
- Greater Middle Eastern: 0.09%
- Publication: Lu X et.al, Neurology (2021-05-24)
- View in PGS-Catalog
Target study
- Coverage: 533 (99.81%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002261
Reference score
- Variants: 22
- Variants ignored: 0
-
Trait: Neuroblastoma
- Mapped Trait(s):
- Samples: 6,303
- Population:
- Publication: Testori A et.al, Cancer Epidemiol Biomarkers Prev (2022-02-07)
- View in PGS-Catalog
Target study
- Coverage: 22 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002262
Reference score
- Variants: 540
- Variants ignored: 0
-
Trait: Coronary artery disease
- Mapped Trait(s):
- Samples: 962,970
- Population:
- East Asian: 99.3%
- Additional Asian Ancestries: 0.7%
- Publication: Lu X et.al, Eur Heart J (2022-02-23)
- View in PGS-Catalog
Target study
- Coverage: 540 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002264
Reference score
- Variants: 49
- Variants ignored: 0
-
Trait: Pancreatic ductal adenocarcinoma
- Mapped Trait(s):
- Samples: 435,847
- Population:
- European: 99.3%
- East Asian: 0.7%
- Publication: Sharma S et.al, Gastroenterology (2022-01-21)
- View in PGS-Catalog
Target study
- Coverage: 49 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002265
Reference score
- Variants: 140
- Variants ignored: 27
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 120,184
- Population:
- Publication: Thomas M et.al, Am J Hum Genet (2020-08-05)
- View in PGS-Catalog
Target study
- Coverage: 109 (77.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002266
Reference score
- Variants: 29
- Variants ignored: 0
-
Trait: Nonsyndromic cleft lip with or without cleft palate
- Mapped Trait(s):
- Samples: 30,822
- Population:
- European: 59.8%
- Additional Asian Ancestries: 20.7%
- Multi-Ancestry (excluding Europeans): 10.3%
- Unknown: 5.1%
- Hispanic or Latin American: 3.5%
- African: 0.6%
- Publication: Yu Y et.al, Hum Mol Genet (2022-02-11)
- View in PGS-Catalog
Target study
- Coverage: 29 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002267
Reference score
- Variants: 89
- Variants ignored: 0
-
Trait: Ascending thoracic aortic diameter
- Mapped Trait(s):
- Samples: 33,637
- Population:
- Publication: Pirruccello JP et.al, Nat Genet (2021-11-26)
- View in PGS-Catalog
Target study
- Coverage: 88 (98.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002268
Reference score
- Variants: 29
- Variants ignored: 8
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 10,187
- Population:
- Publication: Song SH et.al, Investig Clin Urol (2022-01-01)
- View in PGS-Catalog
Target study
- Coverage: 21 (72.41%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002269
Reference score
- Variants: 47
- Variants ignored: 8
-
Trait: Age-related macular degeneration
- Mapped Trait(s):
- Samples: 33,976
- Population:
- Publication: Zekavat SM et.al, Ophthalmology (2022-02-08)
- View in PGS-Catalog
Target study
- Coverage: 37 (78.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002270
Reference score
- Variants: 33
- Variants ignored: 0
-
Trait: Lung cancer
- Mapped Trait(s):
- Samples: 218,879
- Population:
- European: 79.9%
- East Asian: 20.1%
- Publication: Zhang P et.al, Br J Cancer (2022-02-22)
- View in PGS-Catalog
Target study
- Coverage: 33 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002271
Reference score
- Variants: 1,097,364
- Variants ignored: 0
-
Trait: Mitral valve prolapse
- Mapped Trait(s):
- Samples: 46,304
- Population:
- Publication: Roselli C et.al, Eur Heart J (2022-03-04)
- View in PGS-Catalog
Target study
- Coverage: 1,096,537 (99.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002272
Reference score
- Variants: 6
- Variants ignored: 1
-
Trait: COVID-19 infection
- Mapped Trait(s):
- Samples: 127,704
- Population:
- European: 82.3%
- Hispanic or Latin American: 12.2%
- Multi-Ancestry (excluding Europeans): 2.8%
- South Asian: 1.1%
- African: 0.9%
- East Asian: 0.7%
- Publication: Horowitz JE et.al, Nat Genet (2022-03-03)
- View in PGS-Catalog
Target study
- Coverage: 5 (83.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002273
Reference score
- Variants: 12
- Variants ignored: 1
-
Trait: COVID-19 infection
- Mapped Trait(s):
- Samples: 127,704
- Population:
- European: 82.3%
- Hispanic or Latin American: 12.2%
- Multi-Ancestry (excluding Europeans): 2.8%
- South Asian: 1.1%
- African: 0.9%
- East Asian: 0.7%
- Publication: Horowitz JE et.al, Nat Genet (2022-03-03)
- View in PGS-Catalog
Target study
- Coverage: 11 (91.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002274
Reference score
- Variants: 279
- Variants ignored: 0
-
Trait: Low-density lipoprotein cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 237,050
- Population:
- Publication: Groenland EH et.al, Atherosclerosis (2022-03-11)
- View in PGS-Catalog
Target study
- Coverage: 278 (99.64%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002275
Reference score
- Variants: 425
- Variants ignored: 0
-
Trait: Systolic blood pressure
- Mapped Trait(s):
- Samples: 1,363,940
- Population:
- European: 91.2%
- African: 6.2%
- Hispanic or Latin American: 2%
- Additional Asian Ancestries: 0.4%
- Additional Diverse Ancestries: 0.2%
- Publication: Groenland EH et.al, Atherosclerosis (2022-03-11)
- View in PGS-Catalog
Target study
- Coverage: 424 (99.76%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002276
Reference score
- Variants: 1,110,494
- Variants ignored: 0
-
Trait: QTc duration
- Mapped Trait(s):
- Samples: 84,630
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Nauffal V et.al, Circulation (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,110,494 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002277
Reference score
- Variants: 8
- Variants ignored: 0
-
Trait: Type 2 diabetes (based on SNPs associated with insulin secretion)
- Mapped Trait(s):
- Samples: 488,710
- Population:
- European: 68.6%
- Multi-Ancestry (excluding Europeans): 31.4%
- Publication: Siddiqui MK et.al, Diabetologia (2022-03-05)
- View in PGS-Catalog
Target study
- Coverage: 7 (87.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002278
Reference score
- Variants: 16
- Variants ignored: 0
-
Trait: Supranormal left ventricular ejection fraction
- Mapped Trait(s):
- EFO_0008373: left ventricular ejection fraction measurement
- Samples: 30,557
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Forrest IS et.al, Eur J Heart Fail (2022-03-12)
- View in PGS-Catalog
Target study
- Coverage: 15 (93.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002279
Reference score
- Variants: 22
- Variants ignored: 0
-
Trait: Reduced left ventricular ejection fraction
- Mapped Trait(s):
- EFO_0008373: left ventricular ejection fraction measurement
- Samples: 36,041
- Population:
- European: 98.2%
- South Asian: 0.8%
- Unknown: 0.4%
- East Asian: 0.3%
- African: 0.3%
- Publication: Forrest IS et.al, Eur J Heart Fail (2022-03-12)
- View in PGS-Catalog
Target study
- Coverage: 22 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002280
Reference score
- Variants: 83
- Variants ignored: 0
-
Trait: Alzheimer’s disease
- Mapped Trait(s):
- Samples: 487,511
- Population:
- Publication: Bellenguez C et.al, Nat Genet (2022-04-04)
- View in PGS-Catalog
Target study
- Coverage: 82 (98.8%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002281
Reference score
- Variants: 23
- Variants ignored: 0
-
Trait: Multiple myeloma
- Mapped Trait(s):
- Samples: 733,337
- Population:
- Publication: Canzian F et.al, Eur J Hum Genet (2021-11-30)
- View in PGS-Catalog
Target study
- Coverage: 12 (52.17%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002282
Reference score
- Variants: 68
- Variants ignored: 0
-
Trait: Nonalcoholic fatty liver disease
- Mapped Trait(s):
- Samples: 218,595
- Population:
- European: 75.1%
- African: 17.1%
- Hispanic or Latin American: 6.9%
- Additional Asian Ancestries: 0.9%
- Publication: Schnurr TM et.al, Hepatol Commun (2022-03-15)
- View in PGS-Catalog
Target study
- Coverage: 68 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002283
Reference score
- Variants: 15
- Variants ignored: 0
-
Trait: Nonalcoholic fatty liver disease
- Mapped Trait(s):
- Samples: 218,595
- Population:
- European: 75.1%
- African: 17.1%
- Hispanic or Latin American: 6.9%
- Additional Asian Ancestries: 0.9%
- Publication: Schnurr TM et.al, Hepatol Commun (2022-03-15)
- View in PGS-Catalog
Target study
- Coverage: 15 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002284
Reference score
- Variants: 285
- Variants ignored: 0
-
Trait: High density lipoprotein cholesterol
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 312,571
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Kamiza AB et.al, Nat Med (2022-06-02)
- View in PGS-Catalog
Target study
- Coverage: 285 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002285
Reference score
- Variants: 285
- Variants ignored: 0
-
Trait: Low density lipoprotein cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 312,571
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Kamiza AB et.al, Nat Med (2022-06-02)
- View in PGS-Catalog
Target study
- Coverage: 285 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002286
Reference score
- Variants: 285
- Variants ignored: 0
-
Trait: Total cholesterol
- Mapped Trait(s):
- Samples: 312,571
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Kamiza AB et.al, Nat Med (2022-06-02)
- View in PGS-Catalog
Target study
- Coverage: 285 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002287
Reference score
- Variants: 285
- Variants ignored: 0
-
Trait: Triglyceride
- Mapped Trait(s):
- Samples: 312,571
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Kamiza AB et.al, Nat Med (2022-06-02)
- View in PGS-Catalog
Target study
- Coverage: 285 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002288
Reference score
- Variants: 3,242,959
- Variants ignored: 0
-
Trait: Pelvic organ prolapse
- Mapped Trait(s):
- Samples: 447,544
- Population:
- Publication: Pujol-Gualdo N et.al, Nat Commun (2022-06-23)
- View in PGS-Catalog
Target study
- Coverage: 3,193,551 (98.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002289
Reference score
- Variants: 23
- Variants ignored: 6
-
Trait: Late onset Alzheimers disease
- Mapped Trait(s):
- Samples: 55,134
- Population:
- Publication: Zimmerman SC et.al, JAMA Netw Open (2022-04-01)
- View in PGS-Catalog
Target study
- Coverage: 17 (73.91%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002290
Reference score
- Variants: 10
- Variants ignored: 0
-
Trait: Uric acid level
- Mapped Trait(s):
- Samples: 234,754
- Population:
- Publication: Gurung RL et.al, J Clin Endocrinol Metab (2022-04-01)
- View in PGS-Catalog
Target study
- Coverage: 10 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002291
Reference score
- Variants: 12
- Variants ignored: 4
-
Trait: Nasopharyngeal carcinoma
- Mapped Trait(s):
- Samples: 0
- Population:
- Publication: He YQ et.al, Nat Commun (2022-04-12)
- View in PGS-Catalog
Target study
- Coverage: 8 (66.67%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002292
Reference score
- Variants: 36
- Variants ignored: 0
-
Trait: Keratoconus
- Mapped Trait(s):
- Samples: 26,742
- Population:
- Publication: He W et.al, JAMA Ophthalmol (2022-04-21)
- View in PGS-Catalog
Target study
- Coverage: 36 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002293
Reference score
- Variants: 62
- Variants ignored: 11
-
Trait: Psoriasis
- Mapped Trait(s):
- Samples: 287,323
- Population:
- Publication: Shen M et.al, J Am Acad Dermatol (2022-04-12)
- View in PGS-Catalog
Target study
- Coverage: 51 (82.26%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002294
Reference score
- Variants: 111
- Variants ignored: 0
-
Trait: Breast cancer
- Mapped Trait(s):
- Samples: 417,206
- Population:
- European: 88.3%
- East Asian: 11.7%
- Publication: Yang Y et.al, JAMA Netw Open (2022-03-01)
- View in PGS-Catalog
Target study
- Coverage: 111 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002295
Reference score
- Variants: 413
- Variants ignored: 0
-
Trait: Insulin growth-like factor-1 level
- Mapped Trait(s):
- Samples: 988,351
- Population:
- Unknown: 61.1%
- European: 37.6%
- South Asian: 0.7%
- African: 0.6%
- Publication: Tsai CW et.al, American Journal of Cancer Research (2022-02-15)
- View in PGS-Catalog
Target study
- Coverage: 413 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002296
Reference score
- Variants: 2,166
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 458,554
- Population:
- Publication: Maj C et.al, Front Cardiovasc Med (2022-02-16)
- View in PGS-Catalog
Target study
- Coverage: 2,166 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002297
Reference score
- Variants: 48
- Variants ignored: 0
-
Trait: Lipoprotein (a) levels
- Mapped Trait(s):
- Samples: 13,781
- Population:
- Publication: Coassin S et.al, Circ Genom Precis Med (2022-02-08)
- View in PGS-Catalog
Target study
- Coverage: 48 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002298
Reference score
- Variants: 14
- Variants ignored: 7
-
Trait: Esophageal cancer
- Mapped Trait(s):
- Samples: 21,271
- Population:
- Publication: Choi J et.al, Int J Cancer (2020-07-09)
- View in PGS-Catalog
Target study
- Coverage: 7 (50%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002299
Reference score
- Variants: 3
- Variants ignored: 0
-
Trait: Gastric cancer
- Mapped Trait(s):
- Samples: 208,152
- Population:
- Publication: Choi J et.al, Int J Cancer (2020-07-09)
- View in PGS-Catalog
Target study
- Coverage: 3 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002300
Reference score
- Variants: 19
- Variants ignored: 4
-
Trait: Endometrial cancer
- Mapped Trait(s):
- Samples: 121,885
- Population:
- Publication: Choi J et.al, Int J Cancer (2020-07-09)
- View in PGS-Catalog
Target study
- Coverage: 14 (73.68%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002301
Reference score
- Variants: 22
- Variants ignored: 8
-
Trait: Melanoma
- Mapped Trait(s):
- Samples: 291,407
- Population:
- Publication: Choi J et.al, Int J Cancer (2020-07-09)
- View in PGS-Catalog
Target study
- Coverage: 14 (63.64%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002302
Reference score
- Variants: 28
- Variants ignored: 6
-
Trait: Glioma
- Mapped Trait(s):
- Samples: 30,659
- Population:
- Publication: Choi J et.al, Int J Cancer (2020-07-09)
- View in PGS-Catalog
Target study
- Coverage: 22 (78.57%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002303
Reference score
- Variants: 9
- Variants ignored: 2
-
Trait: Diffuse large B-cell lymphoma
- Mapped Trait(s):
- Samples: 11,523
- Population:
- Publication: Choi J et.al, Int J Cancer (2020-07-09)
- View in PGS-Catalog
Target study
- Coverage: 7 (77.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002304
Reference score
- Variants: 6
- Variants ignored: 3
-
Trait: Follicular lymphoma
- Mapped Trait(s):
- Samples: 10,486
- Population:
- Publication: Choi J et.al, Int J Cancer (2020-07-09)
- View in PGS-Catalog
Target study
- Coverage: 3 (50%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002305
Reference score
- Variants: 43
- Variants ignored: 10
-
Trait: Chronic lymphoid leukemia
- Mapped Trait(s):
- Samples: 17,691
- Population:
- Publication: Choi J et.al, Int J Cancer (2020-07-09)
- View in PGS-Catalog
Target study
- Coverage: 33 (76.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002306
Reference score
- Variants: 23
- Variants ignored: 5
-
Trait: Multiple myeloma
- Mapped Trait(s):
- Samples: 249,665
- Population:
- Publication: Choi J et.al, Int J Cancer (2020-07-09)
- View in PGS-Catalog
Target study
- Coverage: 18 (78.26%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002307
Reference score
- Variants: 33
- Variants ignored: 0
-
Trait: Gout
- Mapped Trait(s):
- Samples: 69,374
- Population:
- Publication: Zhang Y et.al, BMC Med (2022-04-29)
- View in PGS-Catalog
Target study
- Coverage: 26 (78.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002308
Reference score
- Variants: 1,259,754
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 1,099,372
- Population:
- European: 81.7%
- East Asian: 16.1%
- African: 2.2%
- Publication: Ge T et.al, Genome Med (2022-06-29)
- View in PGS-Catalog
Target study
- Coverage: 1,259,754 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002309
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Number of children ever born
- Mapped Trait(s):
- Samples: 335,600
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002310
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Age of Menarche
- Mapped Trait(s):
- Samples: 176,155
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002311
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Asthma
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002312
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Autoimmune disease
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002313
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 336,394
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002314
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Balding Type 1
- Mapped Trait(s):
- Samples: 155,100
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002315
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Bone Mineral Density
- Mapped Trait(s):
- Samples: 327,738
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002316
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Cardiovascular disease
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002317
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Childless
- Mapped Trait(s):
- Samples: 335,600
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002318
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Chronotype (morning person)
- Mapped Trait(s):
- Samples: 301,397
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002319
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: College education
- Mapped Trait(s):
- Samples: 334,353
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002320
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Dermatologic diseases
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002321
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Diabetes (any type)
- Mapped Trait(s):
- Samples: 336,759
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002322
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Diastolic blood pressure
- Mapped Trait(s):
- Samples: 310,831
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002323
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Eczema
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002324
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Endocrine and diabetes diseases
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002325
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Eosinophil count
- Mapped Trait(s):
- Samples: 323,358
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002326
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: FEV1/FVC Ratio
- Mapped Trait(s):
- Samples: 274,172
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002327
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Forced Vital Capacity
- Mapped Trait(s):
- Samples: 274,172
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002328
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 291,275
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002329
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: HDL Cholesterol
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 294,075
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002330
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Hair Color
- Mapped Trait(s):
- Samples: 332,641
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002331
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: HbA1c
- Mapped Trait(s):
- Samples: 318,400
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002332
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 336,759
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002333
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: High Light Scatter Reticulocyte Count
- Mapped Trait(s):
- Samples: 321,608
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002334
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: High cholesterol
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002335
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 336,972
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002336
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Hypothyroidism
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002337
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: LDL Cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 321,002
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002338
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Lymphocyte Count
- Mapped Trait(s):
- Samples: 326,304
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002339
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Mean Corpuscular Hemoglobin
- Mapped Trait(s):
- Samples: 326,188
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002340
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Mean Platelet Volume
- Mapped Trait(s):
- Samples: 327,205
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002341
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Monocyte Count
- Mapped Trait(s):
- Samples: 325,319
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002342
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Neuroticism
- Mapped Trait(s):
- Samples: 274,316
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002343
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Platelet count
- Mapped Trait(s):
- Samples: 326,621
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002344
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Psoriasis
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002345
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Red Blood Cell Count
- Mapped Trait(s):
- Samples: 327,209
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002346
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Red Blood Cell Distribution Width
- Mapped Trait(s):
- Samples: 325,395
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002347
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Respiratory and ear-nose-throat diseases
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002348
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Smoking status
- Mapped Trait(s):
- Samples: 336,312
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002349
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 310,831
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002350
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Tanning
- Mapped Trait(s):
- Samples: 330,738
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002351
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Thyroid (self-reported conditions)
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002352
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Total cholesterol
- Mapped Trait(s):
- Samples: 321,595
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002353
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 319,244
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002354
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002355
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 307,287
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002356
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: Waist-Hip Ratio
- Mapped Trait(s):
- Samples: 336,847
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002357
Reference score
- Variants: 1,109,311
- Variants ignored: 0
-
Trait: White Blood Count
- Mapped Trait(s):
- Samples: 326,723
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,109,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002358
Reference score
- Variants: 920,922
- Variants ignored: 0
-
Trait: Asthma
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,922 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002359
Reference score
- Variants: 920,927
- Variants ignored: 0
-
Trait: Autoimmune disease
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,927 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002360
Reference score
- Variants: 920,920
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,920 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002361
Reference score
- Variants: 920,929
- Variants ignored: 0
-
Trait: Cardiovascular disease
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,929 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002362
Reference score
- Variants: 920,925
- Variants ignored: 0
-
Trait: Diastolic blood pressure
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,925 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002363
Reference score
- Variants: 920,927
- Variants ignored: 0
-
Trait: Eczema
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,927 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002364
Reference score
- Variants: 920,929
- Variants ignored: 0
-
Trait: Eosinophil count
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,929 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002365
Reference score
- Variants: 920,926
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,926 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002366
Reference score
- Variants: 920,924
- Variants ignored: 0
-
Trait: HDL Cholesterol
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,924 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002367
Reference score
- Variants: 920,924
- Variants ignored: 0
-
Trait: HbA1c
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,924 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002368
Reference score
- Variants: 920,927
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,927 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002369
Reference score
- Variants: 920,930
- Variants ignored: 0
-
Trait: LDL Cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,930 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002370
Reference score
- Variants: 920,935
- Variants ignored: 0
-
Trait: Lymphocyte Count
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,935 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002371
Reference score
- Variants: 920,923
- Variants ignored: 0
-
Trait: Mean Corpuscular Hemoglobin
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,923 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002372
Reference score
- Variants: 920,930
- Variants ignored: 0
-
Trait: Monocyte Count
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,930 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002373
Reference score
- Variants: 920,923
- Variants ignored: 0
-
Trait: Platelet count
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,923 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002374
Reference score
- Variants: 920,935
- Variants ignored: 0
-
Trait: Red Blood Cell Count
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,935 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002375
Reference score
- Variants: 920,934
- Variants ignored: 0
-
Trait: Smoking status
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,934 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002376
Reference score
- Variants: 920,928
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,928 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002377
Reference score
- Variants: 920,922
- Variants ignored: 0
-
Trait: Total cholesterol
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,922 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002378
Reference score
- Variants: 920,927
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,927 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002379
Reference score
- Variants: 920,930
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,930 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002380
Reference score
- Variants: 920,936
- Variants ignored: 0
-
Trait: White Blood Count
- Mapped Trait(s):
- Samples: 124,000
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 920,936 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002381
Reference score
- Variants: 1,639
- Variants ignored: 0
-
Trait: Number of children ever born
- Mapped Trait(s):
- Samples: 335,600
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,472 (89.81%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002382
Reference score
- Variants: 6,332
- Variants ignored: 0
-
Trait: Age of Menarche
- Mapped Trait(s):
- Samples: 176,155
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 5,930 (93.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002383
Reference score
- Variants: 3,893
- Variants ignored: 0
-
Trait: Asthma
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 3,641 (93.53%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002384
Reference score
- Variants: 2,563
- Variants ignored: 0
-
Trait: Autoimmune disease
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 2,329 (90.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002385
Reference score
- Variants: 15,518
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 336,394
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 14,760 (95.12%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002386
Reference score
- Variants: 7,823
- Variants ignored: 0
-
Trait: Balding Type 1
- Mapped Trait(s):
- Samples: 155,100
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 7,352 (93.98%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002387
Reference score
- Variants: 25,831
- Variants ignored: 0
-
Trait: Bone Mineral Density
- Mapped Trait(s):
- Samples: 327,738
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 24,209 (93.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002388
Reference score
- Variants: 5,621
- Variants ignored: 0
-
Trait: Cardiovascular disease
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 5,257 (93.52%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002389
Reference score
- Variants: 1,578
- Variants ignored: 0
-
Trait: Childless
- Mapped Trait(s):
- Samples: 335,600
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,405 (89.04%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002390
Reference score
- Variants: 3,625
- Variants ignored: 0
-
Trait: Chronotype (morning person)
- Mapped Trait(s):
- Samples: 301,397
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 3,373 (93.05%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002391
Reference score
- Variants: 6,535
- Variants ignored: 0
-
Trait: College education
- Mapped Trait(s):
- Samples: 334,353
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 6,107 (93.45%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002392
Reference score
- Variants: 3,539
- Variants ignored: 0
-
Trait: Dermatologic diseases
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 3,284 (92.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002393
Reference score
- Variants: 3,813
- Variants ignored: 0
-
Trait: Diabetes (any type)
- Mapped Trait(s):
- Samples: 336,759
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 3,549 (93.08%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002394
Reference score
- Variants: 11,460
- Variants ignored: 0
-
Trait: Diastolic blood pressure
- Mapped Trait(s):
- Samples: 310,831
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 10,884 (94.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002395
Reference score
- Variants: 4,367
- Variants ignored: 0
-
Trait: Eczema
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 4,059 (92.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002396
Reference score
- Variants: 3,681
- Variants ignored: 0
-
Trait: Endocrine and diabetes diseases
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 3,419 (92.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002397
Reference score
- Variants: 15,667
- Variants ignored: 0
-
Trait: Eosinophil count
- Mapped Trait(s):
- Samples: 323,358
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 14,685 (93.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002398
Reference score
- Variants: 12,645
- Variants ignored: 0
-
Trait: FEV1/FVC Ratio
- Mapped Trait(s):
- Samples: 274,172
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 11,945 (94.46%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002399
Reference score
- Variants: 9,469
- Variants ignored: 0
-
Trait: Forced Vital Capacity
- Mapped Trait(s):
- Samples: 274,172
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 8,981 (94.85%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002400
Reference score
- Variants: 3,774
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 291,275
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 3,478 (92.16%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002401
Reference score
- Variants: 15,141
- Variants ignored: 0
-
Trait: HDL Cholesterol
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 294,075
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 13,990 (92.4%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002402
Reference score
- Variants: 18,096
- Variants ignored: 0
-
Trait: Hair Color
- Mapped Trait(s):
- Samples: 332,641
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 16,435 (90.82%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002403
Reference score
- Variants: 11,872
- Variants ignored: 0
-
Trait: HbA1c
- Mapped Trait(s):
- Samples: 318,400
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 11,116 (93.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002404
Reference score
- Variants: 56,984
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 336,759
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 53,256 (93.46%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002405
Reference score
- Variants: 16,031
- Variants ignored: 0
-
Trait: High Light Scatter Reticulocyte Count
- Mapped Trait(s):
- Samples: 321,608
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 14,964 (93.34%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002406
Reference score
- Variants: 3,246
- Variants ignored: 0
-
Trait: High cholesterol
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 2,974 (91.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002407
Reference score
- Variants: 6,693
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 336,972
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 6,274 (93.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002408
Reference score
- Variants: 4,815
- Variants ignored: 0
-
Trait: Hypothyroidism
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 4,485 (93.15%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002409
Reference score
- Variants: 7,626
- Variants ignored: 0
-
Trait: LDL Cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 321,002
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 6,995 (91.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002410
Reference score
- Variants: 14,889
- Variants ignored: 0
-
Trait: Lymphocyte Count
- Mapped Trait(s):
- Samples: 326,304
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 14,093 (94.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002411
Reference score
- Variants: 22,349
- Variants ignored: 0
-
Trait: Mean Corpuscular Hemoglobin
- Mapped Trait(s):
- Samples: 326,188
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 20,592 (92.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002412
Reference score
- Variants: 36,285
- Variants ignored: 0
-
Trait: Mean Platelet Volume
- Mapped Trait(s):
- Samples: 327,205
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 33,073 (91.15%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002413
Reference score
- Variants: 17,405
- Variants ignored: 0
-
Trait: Monocyte Count
- Mapped Trait(s):
- Samples: 325,319
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 16,235 (93.28%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002414
Reference score
- Variants: 3,578
- Variants ignored: 0
-
Trait: Neuroticism
- Mapped Trait(s):
- Samples: 274,316
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 3,300 (92.23%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002415
Reference score
- Variants: 27,345
- Variants ignored: 0
-
Trait: Platelet count
- Mapped Trait(s):
- Samples: 326,621
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 25,425 (92.98%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002416
Reference score
- Variants: 6,879
- Variants ignored: 0
-
Trait: Psoriasis
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 6,422 (93.36%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002417
Reference score
- Variants: 18,514
- Variants ignored: 0
-
Trait: Red Blood Cell Count
- Mapped Trait(s):
- Samples: 327,209
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 17,322 (93.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002418
Reference score
- Variants: 16,996
- Variants ignored: 0
-
Trait: Red Blood Cell Distribution Width
- Mapped Trait(s):
- Samples: 325,395
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 15,819 (93.07%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002419
Reference score
- Variants: 3,299
- Variants ignored: 0
-
Trait: Respiratory and ear-nose-throat diseases
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 3,045 (92.3%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002420
Reference score
- Variants: 3,874
- Variants ignored: 0
-
Trait: Smoking status
- Mapped Trait(s):
- Samples: 336,312
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 3,615 (93.31%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002421
Reference score
- Variants: 11,737
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 310,831
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 11,103 (94.6%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002422
Reference score
- Variants: 8,273
- Variants ignored: 0
-
Trait: Tanning
- Mapped Trait(s):
- Samples: 330,738
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 7,282 (88.02%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002423
Reference score
- Variants: 4,483
- Variants ignored: 0
-
Trait: Thyroid (self-reported conditions)
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 4,167 (92.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002424
Reference score
- Variants: 8,526
- Variants ignored: 0
-
Trait: Total cholesterol
- Mapped Trait(s):
- Samples: 321,595
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 7,874 (92.35%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002425
Reference score
- Variants: 10,135
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 319,244
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 9,308 (91.84%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002426
Reference score
- Variants: 3,947
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 3,671 (93.01%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002427
Reference score
- Variants: 4,821
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 307,287
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 4,262 (88.4%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002428
Reference score
- Variants: 9,477
- Variants ignored: 0
-
Trait: Waist-Hip Ratio
- Mapped Trait(s):
- Samples: 336,847
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 8,917 (94.09%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002429
Reference score
- Variants: 13,898
- Variants ignored: 0
-
Trait: White Blood Count
- Mapped Trait(s):
- Samples: 326,723
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 13,087 (94.16%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002430
Reference score
- Variants: 11,512
- Variants ignored: 0
-
Trait: Number of children ever born
- Mapped Trait(s):
- Samples: 335,600
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 9,860 (85.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002431
Reference score
- Variants: 21,880
- Variants ignored: 0
-
Trait: Age of Menarche
- Mapped Trait(s):
- Samples: 176,155
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 19,622 (89.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002432
Reference score
- Variants: 15,843
- Variants ignored: 0
-
Trait: Asthma
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 14,053 (88.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002433
Reference score
- Variants: 13,075
- Variants ignored: 0
-
Trait: Autoimmune disease
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 11,389 (87.11%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002434
Reference score
- Variants: 41,662
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 336,394
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 38,287 (91.9%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002435
Reference score
- Variants: 21,564
- Variants ignored: 0
-
Trait: Balding Type 1
- Mapped Trait(s):
- Samples: 155,100
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 19,258 (89.31%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002436
Reference score
- Variants: 53,472
- Variants ignored: 0
-
Trait: Bone Mineral Density
- Mapped Trait(s):
- Samples: 327,738
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 48,662 (91%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002437
Reference score
- Variants: 20,431
- Variants ignored: 0
-
Trait: Cardiovascular disease
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 18,255 (89.35%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002438
Reference score
- Variants: 10,891
- Variants ignored: 0
-
Trait: Childless
- Mapped Trait(s):
- Samples: 335,600
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 9,409 (86.39%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002439
Reference score
- Variants: 16,590
- Variants ignored: 0
-
Trait: Chronotype (morning person)
- Mapped Trait(s):
- Samples: 301,397
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 14,684 (88.51%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002440
Reference score
- Variants: 24,405
- Variants ignored: 0
-
Trait: College education
- Mapped Trait(s):
- Samples: 334,353
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 21,867 (89.6%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002441
Reference score
- Variants: 14,624
- Variants ignored: 0
-
Trait: Dermatologic diseases
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 12,913 (88.3%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002442
Reference score
- Variants: 15,915
- Variants ignored: 0
-
Trait: Diabetes (any type)
- Mapped Trait(s):
- Samples: 336,759
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 14,154 (88.93%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002443
Reference score
- Variants: 31,790
- Variants ignored: 0
-
Trait: Diastolic blood pressure
- Mapped Trait(s):
- Samples: 310,831
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 29,028 (91.31%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002444
Reference score
- Variants: 16,802
- Variants ignored: 0
-
Trait: Eczema
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 14,876 (88.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002445
Reference score
- Variants: 15,629
- Variants ignored: 0
-
Trait: Endocrine and diabetes diseases
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 13,822 (88.44%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002446
Reference score
- Variants: 35,512
- Variants ignored: 0
-
Trait: Eosinophil count
- Mapped Trait(s):
- Samples: 323,358
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 32,249 (90.81%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002447
Reference score
- Variants: 33,367
- Variants ignored: 0
-
Trait: FEV1/FVC Ratio
- Mapped Trait(s):
- Samples: 274,172
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 30,259 (90.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002448
Reference score
- Variants: 29,603
- Variants ignored: 0
-
Trait: Forced Vital Capacity
- Mapped Trait(s):
- Samples: 274,172
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 26,910 (90.9%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002449
Reference score
- Variants: 15,659
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 291,275
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 13,837 (88.36%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002450
Reference score
- Variants: 35,979
- Variants ignored: 0
-
Trait: HDL Cholesterol
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 294,075
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 32,355 (89.93%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002451
Reference score
- Variants: 35,360
- Variants ignored: 0
-
Trait: Hair Color
- Mapped Trait(s):
- Samples: 332,641
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 31,430 (88.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002452
Reference score
- Variants: 30,603
- Variants ignored: 0
-
Trait: HbA1c
- Mapped Trait(s):
- Samples: 318,400
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 27,618 (90.25%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002453
Reference score
- Variants: 103,911
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 336,759
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 94,839 (91.27%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002454
Reference score
- Variants: 37,335
- Variants ignored: 0
-
Trait: High Light Scatter Reticulocyte Count
- Mapped Trait(s):
- Samples: 321,608
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 33,777 (90.47%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002455
Reference score
- Variants: 13,788
- Variants ignored: 0
-
Trait: High cholesterol
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 11,937 (86.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002456
Reference score
- Variants: 22,539
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 336,972
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 20,272 (89.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002457
Reference score
- Variants: 17,519
- Variants ignored: 0
-
Trait: Hypothyroidism
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 15,599 (89.04%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002458
Reference score
- Variants: 20,708
- Variants ignored: 0
-
Trait: LDL Cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 321,002
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 18,275 (88.25%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002459
Reference score
- Variants: 36,117
- Variants ignored: 0
-
Trait: Lymphocyte Count
- Mapped Trait(s):
- Samples: 326,304
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 32,937 (91.2%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002460
Reference score
- Variants: 44,827
- Variants ignored: 0
-
Trait: Mean Corpuscular Hemoglobin
- Mapped Trait(s):
- Samples: 326,188
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 40,194 (89.66%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002461
Reference score
- Variants: 65,237
- Variants ignored: 0
-
Trait: Mean Platelet Volume
- Mapped Trait(s):
- Samples: 327,205
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 58,334 (89.42%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002462
Reference score
- Variants: 38,012
- Variants ignored: 0
-
Trait: Monocyte Count
- Mapped Trait(s):
- Samples: 325,319
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 34,340 (90.34%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002463
Reference score
- Variants: 16,660
- Variants ignored: 0
-
Trait: Neuroticism
- Mapped Trait(s):
- Samples: 274,316
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 14,646 (87.91%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002464
Reference score
- Variants: 54,318
- Variants ignored: 0
-
Trait: Platelet count
- Mapped Trait(s):
- Samples: 326,621
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 49,303 (90.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002465
Reference score
- Variants: 21,483
- Variants ignored: 0
-
Trait: Psoriasis
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 19,263 (89.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002466
Reference score
- Variants: 41,471
- Variants ignored: 0
-
Trait: Red Blood Cell Count
- Mapped Trait(s):
- Samples: 327,209
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 37,682 (90.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002467
Reference score
- Variants: 36,619
- Variants ignored: 0
-
Trait: Red Blood Cell Distribution Width
- Mapped Trait(s):
- Samples: 325,395
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 33,014 (90.16%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002468
Reference score
- Variants: 14,628
- Variants ignored: 0
-
Trait: Respiratory and ear-nose-throat diseases
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 12,853 (87.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002469
Reference score
- Variants: 17,774
- Variants ignored: 0
-
Trait: Smoking status
- Mapped Trait(s):
- Samples: 336,312
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 15,772 (88.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002470
Reference score
- Variants: 32,439
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 310,831
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 29,576 (91.17%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002471
Reference score
- Variants: 20,040
- Variants ignored: 0
-
Trait: Tanning
- Mapped Trait(s):
- Samples: 330,738
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 17,358 (86.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002472
Reference score
- Variants: 16,694
- Variants ignored: 0
-
Trait: Thyroid (self-reported conditions)
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 14,841 (88.9%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002473
Reference score
- Variants: 22,547
- Variants ignored: 0
-
Trait: Total cholesterol
- Mapped Trait(s):
- Samples: 321,595
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 19,998 (88.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002474
Reference score
- Variants: 27,130
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 319,244
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 24,228 (89.3%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002475
Reference score
- Variants: 16,275
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 14,492 (89.04%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002476
Reference score
- Variants: 16,848
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 307,287
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 14,579 (86.53%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002477
Reference score
- Variants: 27,033
- Variants ignored: 0
-
Trait: Waist-Hip Ratio
- Mapped Trait(s):
- Samples: 336,847
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 24,463 (90.49%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002478
Reference score
- Variants: 35,005
- Variants ignored: 0
-
Trait: White Blood Count
- Mapped Trait(s):
- Samples: 326,723
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 31,807 (90.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002479
Reference score
- Variants: 89,453
- Variants ignored: 0
-
Trait: Number of children ever born
- Mapped Trait(s):
- Samples: 335,600
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 74,935 (83.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002480
Reference score
- Variants: 115,583
- Variants ignored: 0
-
Trait: Age of Menarche
- Mapped Trait(s):
- Samples: 176,155
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 98,875 (85.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002481
Reference score
- Variants: 95,252
- Variants ignored: 0
-
Trait: Asthma
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 80,382 (84.39%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002482
Reference score
- Variants: 88,404
- Variants ignored: 0
-
Trait: Autoimmune disease
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 74,032 (83.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002483
Reference score
- Variants: 162,598
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 336,394
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 141,864 (87.25%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002484
Reference score
- Variants: 106,858
- Variants ignored: 0
-
Trait: Balding Type 1
- Mapped Trait(s):
- Samples: 155,100
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 90,525 (84.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002485
Reference score
- Variants: 171,392
- Variants ignored: 0
-
Trait: Bone Mineral Density
- Mapped Trait(s):
- Samples: 327,738
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 148,718 (86.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002486
Reference score
- Variants: 110,640
- Variants ignored: 0
-
Trait: Cardiovascular disease
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 94,279 (85.21%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002487
Reference score
- Variants: 86,054
- Variants ignored: 0
-
Trait: Childless
- Mapped Trait(s):
- Samples: 335,600
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 71,959 (83.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002488
Reference score
- Variants: 103,314
- Variants ignored: 0
-
Trait: Chronotype (morning person)
- Mapped Trait(s):
- Samples: 301,397
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 87,476 (84.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002489
Reference score
- Variants: 126,911
- Variants ignored: 0
-
Trait: College education
- Mapped Trait(s):
- Samples: 334,353
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 108,308 (85.34%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002490
Reference score
- Variants: 88,324
- Variants ignored: 0
-
Trait: Dermatologic diseases
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 74,491 (84.34%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002491
Reference score
- Variants: 95,066
- Variants ignored: 0
-
Trait: Diabetes (any type)
- Mapped Trait(s):
- Samples: 336,759
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 80,483 (84.66%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002492
Reference score
- Variants: 137,641
- Variants ignored: 0
-
Trait: Diastolic blood pressure
- Mapped Trait(s):
- Samples: 310,831
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 119,229 (86.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002493
Reference score
- Variants: 100,504
- Variants ignored: 0
-
Trait: Eczema
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 85,194 (84.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002494
Reference score
- Variants: 93,293
- Variants ignored: 0
-
Trait: Endocrine and diabetes diseases
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 78,817 (84.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002495
Reference score
- Variants: 135,927
- Variants ignored: 0
-
Trait: Eosinophil count
- Mapped Trait(s):
- Samples: 323,358
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 116,940 (86.03%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002496
Reference score
- Variants: 139,123
- Variants ignored: 0
-
Trait: FEV1/FVC Ratio
- Mapped Trait(s):
- Samples: 274,172
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 120,076 (86.31%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002497
Reference score
- Variants: 134,519
- Variants ignored: 0
-
Trait: Forced Vital Capacity
- Mapped Trait(s):
- Samples: 274,172
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 116,295 (86.45%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002498
Reference score
- Variants: 95,023
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 291,275
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 80,127 (84.32%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002499
Reference score
- Variants: 141,710
- Variants ignored: 0
-
Trait: HDL Cholesterol
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 294,075
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 121,760 (85.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002500
Reference score
- Variants: 128,235
- Variants ignored: 0
-
Trait: Hair Color
- Mapped Trait(s):
- Samples: 332,641
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 109,035 (85.03%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002501
Reference score
- Variants: 128,425
- Variants ignored: 0
-
Trait: HbA1c
- Mapped Trait(s):
- Samples: 318,400
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 110,268 (85.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002502
Reference score
- Variants: 262,080
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 336,759
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 228,903 (87.34%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002503
Reference score
- Variants: 143,701
- Variants ignored: 0
-
Trait: High Light Scatter Reticulocyte Count
- Mapped Trait(s):
- Samples: 321,608
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 123,944 (86.25%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002504
Reference score
- Variants: 90,341
- Variants ignored: 0
-
Trait: High cholesterol
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 75,392 (83.45%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002505
Reference score
- Variants: 115,656
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 336,972
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 98,955 (85.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002506
Reference score
- Variants: 97,010
- Variants ignored: 0
-
Trait: Hypothyroidism
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 82,088 (84.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002507
Reference score
- Variants: 105,053
- Variants ignored: 0
-
Trait: LDL Cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 321,002
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 88,743 (84.47%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002508
Reference score
- Variants: 140,957
- Variants ignored: 0
-
Trait: Lymphocyte Count
- Mapped Trait(s):
- Samples: 326,304
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 121,654 (86.31%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002509
Reference score
- Variants: 151,362
- Variants ignored: 0
-
Trait: Mean Corpuscular Hemoglobin
- Mapped Trait(s):
- Samples: 326,188
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 129,864 (85.8%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002510
Reference score
- Variants: 183,887
- Variants ignored: 0
-
Trait: Mean Platelet Volume
- Mapped Trait(s):
- Samples: 327,205
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 157,906 (85.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002511
Reference score
- Variants: 140,833
- Variants ignored: 0
-
Trait: Monocyte Count
- Mapped Trait(s):
- Samples: 325,319
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 121,085 (85.98%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002512
Reference score
- Variants: 103,865
- Variants ignored: 0
-
Trait: Neuroticism
- Mapped Trait(s):
- Samples: 274,316
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 88,036 (84.76%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002513
Reference score
- Variants: 170,052
- Variants ignored: 0
-
Trait: Platelet count
- Mapped Trait(s):
- Samples: 326,621
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 146,978 (86.43%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002514
Reference score
- Variants: 96,453
- Variants ignored: 0
-
Trait: Psoriasis
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 82,452 (85.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002515
Reference score
- Variants: 150,047
- Variants ignored: 0
-
Trait: Red Blood Cell Count
- Mapped Trait(s):
- Samples: 327,209
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 129,781 (86.49%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002516
Reference score
- Variants: 136,154
- Variants ignored: 0
-
Trait: Red Blood Cell Distribution Width
- Mapped Trait(s):
- Samples: 325,395
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 116,542 (85.6%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002517
Reference score
- Variants: 93,256
- Variants ignored: 0
-
Trait: Respiratory and ear-nose-throat diseases
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 78,534 (84.21%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002518
Reference score
- Variants: 106,902
- Variants ignored: 0
-
Trait: Smoking status
- Mapped Trait(s):
- Samples: 336,312
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 90,852 (84.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002519
Reference score
- Variants: 139,179
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 310,831
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 120,366 (86.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002520
Reference score
- Variants: 100,837
- Variants ignored: 0
-
Trait: Tanning
- Mapped Trait(s):
- Samples: 330,738
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 84,860 (84.16%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002521
Reference score
- Variants: 95,522
- Variants ignored: 0
-
Trait: Thyroid (self-reported conditions)
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 80,611 (84.39%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002522
Reference score
- Variants: 109,026
- Variants ignored: 0
-
Trait: Total cholesterol
- Mapped Trait(s):
- Samples: 321,595
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 92,392 (84.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002523
Reference score
- Variants: 122,153
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 319,244
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 104,404 (85.47%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002524
Reference score
- Variants: 95,287
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 80,642 (84.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002525
Reference score
- Variants: 99,894
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 307,287
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 84,003 (84.09%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002526
Reference score
- Variants: 126,268
- Variants ignored: 0
-
Trait: Waist-Hip Ratio
- Mapped Trait(s):
- Samples: 336,847
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 108,583 (85.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002527
Reference score
- Variants: 141,866
- Variants ignored: 0
-
Trait: White Blood Count
- Mapped Trait(s):
- Samples: 326,723
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 122,541 (86.38%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002528
Reference score
- Variants: 66
- Variants ignored: 0
-
Trait: Number of children ever born
- Mapped Trait(s):
- Samples: 335,600
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 60 (90.91%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002529
Reference score
- Variants: 1,546
- Variants ignored: 0
-
Trait: Age of Menarche
- Mapped Trait(s):
- Samples: 176,155
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,489 (96.31%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002530
Reference score
- Variants: 817
- Variants ignored: 0
-
Trait: Asthma
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 785 (96.08%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002531
Reference score
- Variants: 382
- Variants ignored: 0
-
Trait: Autoimmune disease
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 364 (95.29%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002532
Reference score
- Variants: 4,284
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 336,394
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 4,142 (96.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002533
Reference score
- Variants: 2,899
- Variants ignored: 0
-
Trait: Balding Type 1
- Mapped Trait(s):
- Samples: 155,100
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 2,786 (96.1%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002534
Reference score
- Variants: 11,440
- Variants ignored: 0
-
Trait: Bone Mineral Density
- Mapped Trait(s):
- Samples: 327,738
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 10,905 (95.32%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002535
Reference score
- Variants: 1,218
- Variants ignored: 0
-
Trait: Cardiovascular disease
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,174 (96.39%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002536
Reference score
- Variants: 53
- Variants ignored: 0
-
Trait: Childless
- Mapped Trait(s):
- Samples: 335,600
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 49 (92.45%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002537
Reference score
- Variants: 562
- Variants ignored: 0
-
Trait: Chronotype (morning person)
- Mapped Trait(s):
- Samples: 301,397
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 546 (97.15%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002538
Reference score
- Variants: 1,136
- Variants ignored: 0
-
Trait: College education
- Mapped Trait(s):
- Samples: 334,353
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,096 (96.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002539
Reference score
- Variants: 540
- Variants ignored: 0
-
Trait: Dermatologic diseases
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 530 (98.15%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002540
Reference score
- Variants: 598
- Variants ignored: 0
-
Trait: Diabetes (any type)
- Mapped Trait(s):
- Samples: 336,759
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 576 (96.32%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002541
Reference score
- Variants: 3,531
- Variants ignored: 0
-
Trait: Diastolic blood pressure
- Mapped Trait(s):
- Samples: 310,831
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 3,431 (97.17%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002542
Reference score
- Variants: 1,104
- Variants ignored: 0
-
Trait: Eczema
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,061 (96.11%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002543
Reference score
- Variants: 528
- Variants ignored: 0
-
Trait: Endocrine and diabetes diseases
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 515 (97.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002544
Reference score
- Variants: 6,683
- Variants ignored: 0
-
Trait: Eosinophil count
- Mapped Trait(s):
- Samples: 323,358
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 6,415 (95.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002545
Reference score
- Variants: 4,165
- Variants ignored: 0
-
Trait: FEV1/FVC Ratio
- Mapped Trait(s):
- Samples: 274,172
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 4,023 (96.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002546
Reference score
- Variants: 2,327
- Variants ignored: 0
-
Trait: Forced Vital Capacity
- Mapped Trait(s):
- Samples: 274,172
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 2,252 (96.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002547
Reference score
- Variants: 840
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 291,275
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 820 (97.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002548
Reference score
- Variants: 6,518
- Variants ignored: 0
-
Trait: HDL Cholesterol
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 294,075
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 6,113 (93.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002549
Reference score
- Variants: 10,216
- Variants ignored: 0
-
Trait: Hair Color
- Mapped Trait(s):
- Samples: 332,641
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 9,277 (90.81%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002550
Reference score
- Variants: 4,546
- Variants ignored: 0
-
Trait: HbA1c
- Mapped Trait(s):
- Samples: 318,400
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 4,340 (95.47%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002551
Reference score
- Variants: 27,070
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 336,759
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 25,742 (95.09%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002552
Reference score
- Variants: 6,655
- Variants ignored: 0
-
Trait: High Light Scatter Reticulocyte Count
- Mapped Trait(s):
- Samples: 321,608
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 6,324 (95.03%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002553
Reference score
- Variants: 810
- Variants ignored: 0
-
Trait: High cholesterol
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 769 (94.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002554
Reference score
- Variants: 1,715
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 336,972
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,651 (96.27%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002555
Reference score
- Variants: 986
- Variants ignored: 0
-
Trait: Hypothyroidism
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 948 (96.15%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002556
Reference score
- Variants: 3,244
- Variants ignored: 0
-
Trait: LDL Cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 321,002
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 3,025 (93.25%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002557
Reference score
- Variants: 5,729
- Variants ignored: 0
-
Trait: Lymphocyte Count
- Mapped Trait(s):
- Samples: 326,304
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 5,507 (96.12%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002558
Reference score
- Variants: 10,888
- Variants ignored: 0
-
Trait: Mean Corpuscular Hemoglobin
- Mapped Trait(s):
- Samples: 326,188
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 10,210 (93.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002559
Reference score
- Variants: 19,124
- Variants ignored: 0
-
Trait: Mean Platelet Volume
- Mapped Trait(s):
- Samples: 327,205
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 17,702 (92.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002560
Reference score
- Variants: 7,666
- Variants ignored: 0
-
Trait: Monocyte Count
- Mapped Trait(s):
- Samples: 325,319
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 7,288 (95.07%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002561
Reference score
- Variants: 469
- Variants ignored: 0
-
Trait: Neuroticism
- Mapped Trait(s):
- Samples: 274,316
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 444 (94.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002562
Reference score
- Variants: 12,742
- Variants ignored: 0
-
Trait: Platelet count
- Mapped Trait(s):
- Samples: 326,621
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 12,009 (94.25%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002563
Reference score
- Variants: 1,348
- Variants ignored: 0
-
Trait: Psoriasis
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,310 (97.18%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002564
Reference score
- Variants: 7,590
- Variants ignored: 0
-
Trait: Red Blood Cell Count
- Mapped Trait(s):
- Samples: 327,209
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 7,202 (94.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002565
Reference score
- Variants: 7,740
- Variants ignored: 0
-
Trait: Red Blood Cell Distribution Width
- Mapped Trait(s):
- Samples: 325,395
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 7,323 (94.61%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002566
Reference score
- Variants: 658
- Variants ignored: 0
-
Trait: Respiratory and ear-nose-throat diseases
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 634 (96.35%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002567
Reference score
- Variants: 517
- Variants ignored: 0
-
Trait: Smoking status
- Mapped Trait(s):
- Samples: 336,312
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 495 (95.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002568
Reference score
- Variants: 3,510
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 310,831
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 3,393 (96.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002569
Reference score
- Variants: 4,792
- Variants ignored: 0
-
Trait: Tanning
- Mapped Trait(s):
- Samples: 330,738
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 4,265 (89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002570
Reference score
- Variants: 954
- Variants ignored: 0
-
Trait: Thyroid (self-reported conditions)
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 917 (96.12%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002571
Reference score
- Variants: 3,573
- Variants ignored: 0
-
Trait: Total cholesterol
- Mapped Trait(s):
- Samples: 321,595
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 3,365 (94.18%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002572
Reference score
- Variants: 3,917
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 319,244
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 3,671 (93.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002573
Reference score
- Variants: 673
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 654 (97.18%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002574
Reference score
- Variants: 1,677
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 307,287
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,484 (88.49%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002575
Reference score
- Variants: 2,912
- Variants ignored: 0
-
Trait: Waist-Hip Ratio
- Mapped Trait(s):
- Samples: 336,847
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 2,780 (95.47%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002576
Reference score
- Variants: 4,921
- Variants ignored: 0
-
Trait: White Blood Count
- Mapped Trait(s):
- Samples: 326,723
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 4,720 (95.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002577
Reference score
- Variants: 21
- Variants ignored: 0
-
Trait: Number of children ever born
- Mapped Trait(s):
- Samples: 335,600
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 20 (95.24%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002578
Reference score
- Variants: 891
- Variants ignored: 0
-
Trait: Age of Menarche
- Mapped Trait(s):
- Samples: 176,155
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 864 (96.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002579
Reference score
- Variants: 503
- Variants ignored: 0
-
Trait: Asthma
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 489 (97.22%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002580
Reference score
- Variants: 206
- Variants ignored: 0
-
Trait: Autoimmune disease
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 198 (96.12%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002581
Reference score
- Variants: 2,385
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 336,394
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 2,314 (97.02%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002582
Reference score
- Variants: 1,998
- Variants ignored: 0
-
Trait: Balding Type 1
- Mapped Trait(s):
- Samples: 155,100
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,926 (96.4%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002583
Reference score
- Variants: 7,908
- Variants ignored: 0
-
Trait: Bone Mineral Density
- Mapped Trait(s):
- Samples: 327,738
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 7,559 (95.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002584
Reference score
- Variants: 637
- Variants ignored: 0
-
Trait: Cardiovascular disease
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 616 (96.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002585
Reference score
- Variants: 12
- Variants ignored: 0
-
Trait: Childless
- Mapped Trait(s):
- Samples: 335,600
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 12 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002586
Reference score
- Variants: 255
- Variants ignored: 0
-
Trait: Chronotype (morning person)
- Mapped Trait(s):
- Samples: 301,397
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 252 (98.82%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002587
Reference score
- Variants: 514
- Variants ignored: 0
-
Trait: College education
- Mapped Trait(s):
- Samples: 334,353
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 500 (97.28%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002588
Reference score
- Variants: 240
- Variants ignored: 0
-
Trait: Dermatologic diseases
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 235 (97.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002589
Reference score
- Variants: 267
- Variants ignored: 0
-
Trait: Diabetes (any type)
- Mapped Trait(s):
- Samples: 336,759
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 259 (97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002590
Reference score
- Variants: 2,090
- Variants ignored: 0
-
Trait: Diastolic blood pressure
- Mapped Trait(s):
- Samples: 310,831
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 2,027 (96.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002591
Reference score
- Variants: 667
- Variants ignored: 0
-
Trait: Eczema
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 641 (96.1%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002592
Reference score
- Variants: 187
- Variants ignored: 0
-
Trait: Endocrine and diabetes diseases
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 184 (98.4%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002593
Reference score
- Variants: 4,677
- Variants ignored: 0
-
Trait: Eosinophil count
- Mapped Trait(s):
- Samples: 323,358
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 4,496 (96.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002594
Reference score
- Variants: 2,609
- Variants ignored: 0
-
Trait: FEV1/FVC Ratio
- Mapped Trait(s):
- Samples: 274,172
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 2,529 (96.93%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002595
Reference score
- Variants: 1,235
- Variants ignored: 0
-
Trait: Forced Vital Capacity
- Mapped Trait(s):
- Samples: 274,172
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,195 (96.76%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002596
Reference score
- Variants: 482
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 291,275
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 473 (98.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002597
Reference score
- Variants: 4,738
- Variants ignored: 0
-
Trait: HDL Cholesterol
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 294,075
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 4,459 (94.11%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002598
Reference score
- Variants: 8,312
- Variants ignored: 0
-
Trait: Hair Color
- Mapped Trait(s):
- Samples: 332,641
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 7,564 (91%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002599
Reference score
- Variants: 3,055
- Variants ignored: 0
-
Trait: HbA1c
- Mapped Trait(s):
- Samples: 318,400
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 2,923 (95.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002600
Reference score
- Variants: 18,937
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 336,759
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 18,095 (95.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002601
Reference score
- Variants: 4,569
- Variants ignored: 0
-
Trait: High Light Scatter Reticulocyte Count
- Mapped Trait(s):
- Samples: 321,608
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 4,356 (95.34%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002602
Reference score
- Variants: 545
- Variants ignored: 0
-
Trait: High cholesterol
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 523 (95.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002603
Reference score
- Variants: 949
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 336,972
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 919 (96.84%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002604
Reference score
- Variants: 550
- Variants ignored: 0
-
Trait: Hypothyroidism
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 525 (95.45%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002605
Reference score
- Variants: 2,337
- Variants ignored: 0
-
Trait: LDL Cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 321,002
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 2,192 (93.8%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002606
Reference score
- Variants: 3,808
- Variants ignored: 0
-
Trait: Lymphocyte Count
- Mapped Trait(s):
- Samples: 326,304
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 3,663 (96.19%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002607
Reference score
- Variants: 8,017
- Variants ignored: 0
-
Trait: Mean Corpuscular Hemoglobin
- Mapped Trait(s):
- Samples: 326,188
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 7,533 (93.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002608
Reference score
- Variants: 14,380
- Variants ignored: 0
-
Trait: Mean Platelet Volume
- Mapped Trait(s):
- Samples: 327,205
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 13,371 (92.98%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002609
Reference score
- Variants: 5,367
- Variants ignored: 0
-
Trait: Monocyte Count
- Mapped Trait(s):
- Samples: 325,319
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 5,120 (95.4%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002610
Reference score
- Variants: 196
- Variants ignored: 0
-
Trait: Neuroticism
- Mapped Trait(s):
- Samples: 274,316
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 182 (92.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002611
Reference score
- Variants: 9,050
- Variants ignored: 0
-
Trait: Platelet count
- Mapped Trait(s):
- Samples: 326,621
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 8,562 (94.61%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002612
Reference score
- Variants: 643
- Variants ignored: 0
-
Trait: Psoriasis
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 632 (98.29%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002613
Reference score
- Variants: 5,156
- Variants ignored: 0
-
Trait: Red Blood Cell Count
- Mapped Trait(s):
- Samples: 327,209
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 4,899 (95.02%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002614
Reference score
- Variants: 5,543
- Variants ignored: 0
-
Trait: Red Blood Cell Distribution Width
- Mapped Trait(s):
- Samples: 325,395
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 5,270 (95.07%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002615
Reference score
- Variants: 382
- Variants ignored: 0
-
Trait: Respiratory and ear-nose-throat diseases
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 371 (97.12%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002616
Reference score
- Variants: 201
- Variants ignored: 0
-
Trait: Smoking status
- Mapped Trait(s):
- Samples: 336,312
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 192 (95.52%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002617
Reference score
- Variants: 2,060
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 310,831
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,996 (96.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002618
Reference score
- Variants: 4,026
- Variants ignored: 0
-
Trait: Tanning
- Mapped Trait(s):
- Samples: 330,738
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 3,605 (89.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002619
Reference score
- Variants: 548
- Variants ignored: 0
-
Trait: Thyroid (self-reported conditions)
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 525 (95.8%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002620
Reference score
- Variants: 2,571
- Variants ignored: 0
-
Trait: Total cholesterol
- Mapped Trait(s):
- Samples: 321,595
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 2,420 (94.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002621
Reference score
- Variants: 2,757
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 319,244
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 2,588 (93.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002622
Reference score
- Variants: 293
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 288 (98.29%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002623
Reference score
- Variants: 1,183
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 307,287
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,055 (89.18%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002624
Reference score
- Variants: 1,829
- Variants ignored: 0
-
Trait: Waist-Hip Ratio
- Mapped Trait(s):
- Samples: 336,847
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 1,741 (95.19%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002625
Reference score
- Variants: 3,184
- Variants ignored: 0
-
Trait: White Blood Count
- Mapped Trait(s):
- Samples: 326,723
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 3,069 (96.39%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002626
Reference score
- Variants: 208,715
- Variants ignored: 0
-
Trait: Number of children ever born
- Mapped Trait(s):
- Samples: 335,600
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 189,171 (90.64%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002627
Reference score
- Variants: 831,098
- Variants ignored: 0
-
Trait: Age of Menarche
- Mapped Trait(s):
- Samples: 176,155
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 755,996 (90.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002628
Reference score
- Variants: 205,286
- Variants ignored: 0
-
Trait: Asthma
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 186,286 (90.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002629
Reference score
- Variants: 159,127
- Variants ignored: 0
-
Trait: Autoimmune disease
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 143,006 (89.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002630
Reference score
- Variants: 620,484
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 336,394
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 586,093 (94.46%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002631
Reference score
- Variants: 877,406
- Variants ignored: 0
-
Trait: Balding Type 1
- Mapped Trait(s):
- Samples: 155,100
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 790,618 (90.11%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002632
Reference score
- Variants: 432,286
- Variants ignored: 0
-
Trait: Bone Mineral Density
- Mapped Trait(s):
- Samples: 327,738
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 403,562 (93.36%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002633
Reference score
- Variants: 381,036
- Variants ignored: 0
-
Trait: Cardiovascular disease
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 353,275 (92.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002634
Reference score
- Variants: 176,147
- Variants ignored: 0
-
Trait: Childless
- Mapped Trait(s):
- Samples: 335,600
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 158,841 (90.18%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002635
Reference score
- Variants: 404,978
- Variants ignored: 0
-
Trait: Chronotype (morning person)
- Mapped Trait(s):
- Samples: 301,397
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 378,441 (93.45%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002636
Reference score
- Variants: 577,448
- Variants ignored: 0
-
Trait: College education
- Mapped Trait(s):
- Samples: 334,353
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 538,929 (93.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002637
Reference score
- Variants: 164,178
- Variants ignored: 0
-
Trait: Dermatologic diseases
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 144,132 (87.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002638
Reference score
- Variants: 247,386
- Variants ignored: 0
-
Trait: Diabetes (any type)
- Mapped Trait(s):
- Samples: 336,759
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 224,229 (90.64%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002639
Reference score
- Variants: 539,912
- Variants ignored: 0
-
Trait: Diastolic blood pressure
- Mapped Trait(s):
- Samples: 310,831
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 503,028 (93.17%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002640
Reference score
- Variants: 241,530
- Variants ignored: 0
-
Trait: Eczema
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 220,291 (91.21%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002641
Reference score
- Variants: 256,678
- Variants ignored: 0
-
Trait: Endocrine and diabetes diseases
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 231,558 (90.21%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002642
Reference score
- Variants: 346,331
- Variants ignored: 0
-
Trait: Eosinophil count
- Mapped Trait(s):
- Samples: 323,358
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 321,308 (92.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002643
Reference score
- Variants: 508,629
- Variants ignored: 0
-
Trait: FEV1/FVC Ratio
- Mapped Trait(s):
- Samples: 274,172
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 472,699 (92.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002644
Reference score
- Variants: 592,696
- Variants ignored: 0
-
Trait: Forced Vital Capacity
- Mapped Trait(s):
- Samples: 274,172
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 547,600 (92.39%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002645
Reference score
- Variants: 412,574
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 291,275
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 370,633 (89.83%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002646
Reference score
- Variants: 402,183
- Variants ignored: 0
-
Trait: HDL Cholesterol
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 294,075
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 372,758 (92.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002647
Reference score
- Variants: 143,829
- Variants ignored: 0
-
Trait: Hair Color
- Mapped Trait(s):
- Samples: 332,641
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 134,777 (93.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002648
Reference score
- Variants: 394,312
- Variants ignored: 0
-
Trait: HbA1c
- Mapped Trait(s):
- Samples: 318,400
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 364,921 (92.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002649
Reference score
- Variants: 478,839
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 336,759
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 455,196 (95.06%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002650
Reference score
- Variants: 406,785
- Variants ignored: 0
-
Trait: High Light Scatter Reticulocyte Count
- Mapped Trait(s):
- Samples: 321,608
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 379,999 (93.42%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002651
Reference score
- Variants: 195,463
- Variants ignored: 0
-
Trait: High cholesterol
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 176,176 (90.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002652
Reference score
- Variants: 385,766
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 336,972
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 357,908 (92.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002653
Reference score
- Variants: 197,450
- Variants ignored: 0
-
Trait: Hypothyroidism
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 178,642 (90.47%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002654
Reference score
- Variants: 274,585
- Variants ignored: 0
-
Trait: LDL Cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 321,002
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 249,509 (90.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002655
Reference score
- Variants: 472,203
- Variants ignored: 0
-
Trait: Lymphocyte Count
- Mapped Trait(s):
- Samples: 326,304
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 437,372 (92.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002656
Reference score
- Variants: 351,633
- Variants ignored: 0
-
Trait: Mean Corpuscular Hemoglobin
- Mapped Trait(s):
- Samples: 326,188
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 323,470 (91.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002657
Reference score
- Variants: 354,280
- Variants ignored: 0
-
Trait: Mean Platelet Volume
- Mapped Trait(s):
- Samples: 327,205
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 327,742 (92.51%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002658
Reference score
- Variants: 353,881
- Variants ignored: 0
-
Trait: Monocyte Count
- Mapped Trait(s):
- Samples: 325,319
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 327,527 (92.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002659
Reference score
- Variants: 546,323
- Variants ignored: 0
-
Trait: Neuroticism
- Mapped Trait(s):
- Samples: 274,316
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 503,771 (92.21%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002660
Reference score
- Variants: 396,074
- Variants ignored: 0
-
Trait: Platelet count
- Mapped Trait(s):
- Samples: 326,621
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 370,113 (93.45%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002661
Reference score
- Variants: 283,128
- Variants ignored: 0
-
Trait: Psoriasis
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 243,852 (86.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002662
Reference score
- Variants: 473,515
- Variants ignored: 0
-
Trait: Red Blood Cell Count
- Mapped Trait(s):
- Samples: 327,209
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 438,730 (92.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002663
Reference score
- Variants: 340,172
- Variants ignored: 0
-
Trait: Red Blood Cell Distribution Width
- Mapped Trait(s):
- Samples: 325,395
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 313,110 (92.04%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002664
Reference score
- Variants: 207,930
- Variants ignored: 0
-
Trait: Respiratory and ear-nose-throat diseases
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 188,449 (90.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002665
Reference score
- Variants: 340,836
- Variants ignored: 0
-
Trait: Smoking status
- Mapped Trait(s):
- Samples: 336,312
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 314,367 (92.23%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002666
Reference score
- Variants: 548,088
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 310,831
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 510,285 (93.1%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002667
Reference score
- Variants: 123,613
- Variants ignored: 0
-
Trait: Tanning
- Mapped Trait(s):
- Samples: 330,738
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 114,700 (92.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002668
Reference score
- Variants: 189,808
- Variants ignored: 0
-
Trait: Thyroid (self-reported conditions)
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 171,747 (90.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002669
Reference score
- Variants: 309,475
- Variants ignored: 0
-
Trait: Total cholesterol
- Mapped Trait(s):
- Samples: 321,595
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 281,318 (90.9%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002670
Reference score
- Variants: 379,622
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 319,244
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 350,113 (92.23%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002671
Reference score
- Variants: 258,382
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 233,047 (90.19%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002672
Reference score
- Variants: 330,506
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 307,287
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 306,100 (92.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002673
Reference score
- Variants: 325,206
- Variants ignored: 0
-
Trait: Waist-Hip Ratio
- Mapped Trait(s):
- Samples: 336,847
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 303,637 (93.37%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002674
Reference score
- Variants: 491,764
- Variants ignored: 0
-
Trait: White Blood Count
- Mapped Trait(s):
- Samples: 326,723
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 455,996 (92.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002675
Reference score
- Variants: 981,889
- Variants ignored: 0
-
Trait: Number of children ever born
- Mapped Trait(s):
- Samples: 335,600
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 981,889 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002676
Reference score
- Variants: 988,120
- Variants ignored: 0
-
Trait: Age of Menarche
- Mapped Trait(s):
- Samples: 176,155
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 988,120 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002677
Reference score
- Variants: 934,369
- Variants ignored: 0
-
Trait: Asthma
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 934,369 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002678
Reference score
- Variants: 923,726
- Variants ignored: 0
-
Trait: Autoimmune disease
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 923,726 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002679
Reference score
- Variants: 987,879
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 336,394
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 987,879 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002680
Reference score
- Variants: 965,079
- Variants ignored: 0
-
Trait: Balding Type 1
- Mapped Trait(s):
- Samples: 155,100
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 965,079 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002681
Reference score
- Variants: 984,276
- Variants ignored: 0
-
Trait: Bone Mineral Density
- Mapped Trait(s):
- Samples: 327,738
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 984,276 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002682
Reference score
- Variants: 972,965
- Variants ignored: 0
-
Trait: Cardiovascular disease
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 972,965 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002683
Reference score
- Variants: 954,898
- Variants ignored: 0
-
Trait: Childless
- Mapped Trait(s):
- Samples: 335,600
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 954,898 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002684
Reference score
- Variants: 977,159
- Variants ignored: 0
-
Trait: Chronotype (morning person)
- Mapped Trait(s):
- Samples: 301,397
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 977,159 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002685
Reference score
- Variants: 980,529
- Variants ignored: 0
-
Trait: College education
- Mapped Trait(s):
- Samples: 334,353
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 980,529 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002686
Reference score
- Variants: 815,851
- Variants ignored: 0
-
Trait: Dermatologic diseases
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 815,851 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002687
Reference score
- Variants: 923,080
- Variants ignored: 0
-
Trait: Diabetes (any type)
- Mapped Trait(s):
- Samples: 336,759
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 923,080 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002688
Reference score
- Variants: 985,844
- Variants ignored: 0
-
Trait: Diastolic blood pressure
- Mapped Trait(s):
- Samples: 310,831
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 985,844 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002689
Reference score
- Variants: 957,578
- Variants ignored: 0
-
Trait: Eczema
- Mapped Trait(s):
- Samples: 337,071
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 957,578 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002690
Reference score
- Variants: 905,637
- Variants ignored: 0
-
Trait: Endocrine and diabetes diseases
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 905,637 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002691
Reference score
- Variants: 980,421
- Variants ignored: 0
-
Trait: Eosinophil count
- Mapped Trait(s):
- Samples: 323,358
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 980,421 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002692
Reference score
- Variants: 985,212
- Variants ignored: 0
-
Trait: FEV1/FVC Ratio
- Mapped Trait(s):
- Samples: 274,172
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 985,212 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002693
Reference score
- Variants: 986,815
- Variants ignored: 0
-
Trait: Forced Vital Capacity
- Mapped Trait(s):
- Samples: 274,172
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 986,815 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002694
Reference score
- Variants: 969,640
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 291,275
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 969,640 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002695
Reference score
- Variants: 971,682
- Variants ignored: 0
-
Trait: HDL Cholesterol
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 294,075
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 971,682 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002696
Reference score
- Variants: 924,497
- Variants ignored: 0
-
Trait: Hair Color
- Mapped Trait(s):
- Samples: 332,641
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 924,497 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002697
Reference score
- Variants: 989,344
- Variants ignored: 0
-
Trait: HbA1c
- Mapped Trait(s):
- Samples: 318,400
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 989,344 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002698
Reference score
- Variants: 986,966
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 336,759
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 986,966 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002699
Reference score
- Variants: 983,680
- Variants ignored: 0
-
Trait: High Light Scatter Reticulocyte Count
- Mapped Trait(s):
- Samples: 321,608
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 983,680 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002700
Reference score
- Variants: 937,601
- Variants ignored: 0
-
Trait: High cholesterol
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 937,601 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002701
Reference score
- Variants: 973,782
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 336,972
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 973,782 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002702
Reference score
- Variants: 889,041
- Variants ignored: 0
-
Trait: Hypothyroidism
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 889,041 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002703
Reference score
- Variants: 970,081
- Variants ignored: 0
-
Trait: LDL Cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 321,002
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 970,081 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002704
Reference score
- Variants: 983,350
- Variants ignored: 0
-
Trait: Lymphocyte Count
- Mapped Trait(s):
- Samples: 326,304
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 983,350 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002705
Reference score
- Variants: 979,778
- Variants ignored: 0
-
Trait: Mean Corpuscular Hemoglobin
- Mapped Trait(s):
- Samples: 326,188
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 979,778 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002706
Reference score
- Variants: 973,986
- Variants ignored: 0
-
Trait: Mean Platelet Volume
- Mapped Trait(s):
- Samples: 327,205
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 973,986 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002707
Reference score
- Variants: 980,307
- Variants ignored: 0
-
Trait: Monocyte Count
- Mapped Trait(s):
- Samples: 325,319
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 980,307 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002708
Reference score
- Variants: 989,963
- Variants ignored: 0
-
Trait: Neuroticism
- Mapped Trait(s):
- Samples: 274,316
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 989,963 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002709
Reference score
- Variants: 981,460
- Variants ignored: 0
-
Trait: Platelet count
- Mapped Trait(s):
- Samples: 326,621
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 981,460 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002710
Reference score
- Variants: 566,839
- Variants ignored: 0
-
Trait: Psoriasis
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 566,839 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002711
Reference score
- Variants: 982,902
- Variants ignored: 0
-
Trait: Red Blood Cell Count
- Mapped Trait(s):
- Samples: 327,209
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 982,902 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002712
Reference score
- Variants: 976,311
- Variants ignored: 0
-
Trait: Red Blood Cell Distribution Width
- Mapped Trait(s):
- Samples: 325,395
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 976,311 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002713
Reference score
- Variants: 940,620
- Variants ignored: 0
-
Trait: Respiratory and ear-nose-throat diseases
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 940,620 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002714
Reference score
- Variants: 981,081
- Variants ignored: 0
-
Trait: Smoking status
- Mapped Trait(s):
- Samples: 336,312
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 981,081 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002715
Reference score
- Variants: 985,820
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 310,831
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 985,820 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002716
Reference score
- Variants: 947,237
- Variants ignored: 0
-
Trait: Tanning
- Mapped Trait(s):
- Samples: 330,738
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 947,237 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002717
Reference score
- Variants: 895,602
- Variants ignored: 0
-
Trait: Thyroid (self-reported conditions)
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 895,602 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002718
Reference score
- Variants: 977,049
- Variants ignored: 0
-
Trait: Total cholesterol
- Mapped Trait(s):
- Samples: 321,595
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 977,049 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002719
Reference score
- Variants: 981,472
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 319,244
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 981,472 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002720
Reference score
- Variants: 911,809
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 337,488
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 911,809 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002721
Reference score
- Variants: 981,998
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 307,287
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 981,998 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002722
Reference score
- Variants: 984,160
- Variants ignored: 0
-
Trait: Waist-Hip Ratio
- Mapped Trait(s):
- Samples: 336,847
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 984,160 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002723
Reference score
- Variants: 983,751
- Variants ignored: 0
-
Trait: White Blood Count
- Mapped Trait(s):
- Samples: 326,723
- Population:
- Publication: Weissbrod O et.al, Nat Genet (2022-04-07)
- View in PGS-Catalog
Target study
- Coverage: 983,751 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002724
Reference score
- Variants: 1,213,574
- Variants ignored: 0
-
Trait: Ischemic stroke
- Mapped Trait(s):
- Samples: 12,788,906
- Population:
- European: 63.2%
- Multi-Ancestry (including Europeans): 32.8%
- Unknown: 3.6%
- South Asian: 0.2%
- East Asian: 0.09%
- Hispanic or Latin American: 0.03%
- African: 0.02%
- Greater Middle Eastern: 0.02%
- Publication: Mishra A et.al, Nature (2022-09-30)
- View in PGS-Catalog
Target study
- Coverage: 1,213,574 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002725
Reference score
- Variants: 6,010,730
- Variants ignored: 0
-
Trait: Ischemic stroke
- Mapped Trait(s):
- Samples: 1,500,781
- Population:
- Publication: Mishra A et.al, Nature (2022-09-30)
- View in PGS-Catalog
Target study
- Coverage: 6,010,730 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002727
Reference score
- Variants: 985,837
- Variants ignored: 0
-
Trait: Asthma
- Mapped Trait(s):
- Samples: 142,486
- Population:
- European: 89.6%
- Multi-Ancestry (excluding Europeans): 5.8%
- East Asian: 3.7%
- Hispanic or Latin American: 1%
- Publication: Namjou B et.al, J Allergy Clin Immunol (2022-05-18)
- View in PGS-Catalog
Target study
- Coverage: 985,836 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002728
Reference score
- Variants: 44
- Variants ignored: 0
-
Trait: Hip osteoarthritis
- Mapped Trait(s):
- Samples: 353,388
- Population:
- Publication: Sedaghati-Khayat B et.al, Arthritis Rheumatol (2022-05-29)
- View in PGS-Catalog
Target study
- Coverage: 41 (93.18%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002729
Reference score
- Variants: 24
- Variants ignored: 0
-
Trait: Knee osteoarthritis
- Mapped Trait(s):
- Samples: 396,044
- Population:
- European: 98.9%
- East Asian: 1.1%
- Publication: Sedaghati-Khayat B et.al, Arthritis Rheumatol (2022-05-29)
- View in PGS-Catalog
Target study
- Coverage: 24 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002730
Reference score
- Variants: 35
- Variants ignored: 5
-
Trait: LDL lowering in response to statin
- Mapped Trait(s):
- Samples: 18,596
- Population:
- Publication: Mayerhofer E et.al, Brain (2022-05-22)
- View in PGS-Catalog
Target study
- Coverage: 30 (85.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002731
Reference score
- Variants: 17
- Variants ignored: 0
-
Trait: Alzheimer’s disease
- Mapped Trait(s):
- Samples: 0
- Population:
- Publication: Xicota L et.al, Neurology (2022-05-23)
- View in PGS-Catalog
Target study
- Coverage: 16 (94.12%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002732
Reference score
- Variants: 77
- Variants ignored: 0
-
Trait: Chronic elevation of alanine aminotransferase
- Mapped Trait(s):
- EFO_0004735: serum alanine aminotransferase measurement
- Samples: 218,595
- Population:
- European: 75.1%
- African: 17.1%
- Hispanic or Latin American: 6.9%
- Additional Asian Ancestries: 0.9%
- Publication: Vujkovic M et.al, Nat Genet (2022-06-02)
- View in PGS-Catalog
Target study
- Coverage: 77 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002733
Reference score
- Variants: 17
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 159,208
- Population:
- Publication: Pezzilli S et.al, Diabetes Metab (2022-04-26)
- View in PGS-Catalog
Target study
- Coverage: 16 (94.12%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002734
Reference score
- Variants: 362
- Variants ignored: 81
-
Trait: Systolic blood pressure
- Mapped Trait(s):
- Samples: 757,601
- Population:
- Publication: Marques-Vidal P et.al, J Hypertens (2022-06-10)
- View in PGS-Catalog
Target study
- Coverage: 272 (75.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002735
Reference score
- Variants: 19
- Variants ignored: 0
-
Trait: Endometrial cancer
- Mapped Trait(s):
- Samples: 0
- Population:
- Publication: Bafligil C et.al, Genet Med (2022-06-15)
- View in PGS-Catalog
Target study
- Coverage: 18 (94.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002736
Reference score
- Variants: 24
- Variants ignored: 0
-
Trait: Endometrial cancer
- Mapped Trait(s):
- Samples: 0
- Population:
- Publication: Bafligil C et.al, Genet Med (2022-06-15)
- View in PGS-Catalog
Target study
- Coverage: 21 (87.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002737
Reference score
- Variants: 72
- Variants ignored: 0
-
Trait: Endometrial cancer
- Mapped Trait(s):
- Samples: 0
- Population:
- Publication: Bafligil C et.al, Genet Med (2022-06-15)
- View in PGS-Catalog
Target study
- Coverage: 68 (94.44%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002738
Reference score
- Variants: 326,000
- Variants ignored: 0
-
Trait: Alcohol use disorder
- Mapped Trait(s):
- Samples: 395,995
- Population:
- European: 81.7%
- African: 14.3%
- Hispanic or Latin American: 3.6%
- East Asian: 0.3%
- South Asian: 0.05%
- Publication: Lai D et.al, Alcohol Clin Exp Res (2022-03-10)
- View in PGS-Catalog
Target study
- Coverage: 326,000 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002739
Reference score
- Variants: 858
- Variants ignored: 0
-
Trait: Alcohol use disorder
- Mapped Trait(s):
- Samples: 492,211
- Population:
- European: 88.5%
- African: 11.5%
- Publication: Lai D et.al, Transl Psychiatry (2022-07-05)
- View in PGS-Catalog
Target study
- Coverage: 858 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002740
Reference score
- Variants: 22
- Variants ignored: 2
-
Trait: Pancreatic cancer
- Mapped Trait(s):
- Samples: 68,762
- Population:
- European: 88.1%
- Unknown: 10.2%
- Multi-Ancestry (excluding Europeans): 0.9%
- Additional Diverse Ancestries: 0.5%
- East Asian: 0.2%
- Publication: Yuan C et.al, Ann Oncol (2022-04-06)
- View in PGS-Catalog
Target study
- Coverage: 20 (90.91%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002741
Reference score
- Variants: 127
- Variants ignored: 0
-
Trait: Primary open-angle glaucoma
- Mapped Trait(s):
- Samples: 383,500
- Population:
- European: 86.3%
- East Asian: 12.1%
- African: 1.6%
- Publication: Waksmunski AR et.al, Ophthalmology (2022-06-16)
- View in PGS-Catalog
Target study
- Coverage: 123 (96.85%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002742
Reference score
- Variants: 115
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 495,045
- Population:
- European: 61.9%
- East Asian: 36.5%
- African: 1.3%
- Additional Diverse Ancestries: 0.2%
- Publication: Ping J et.al, Int J Cancer (2022-06-29)
- View in PGS-Catalog
Target study
- Coverage: 114 (99.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002743
Reference score
- Variants: 115
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 495,045
- Population:
- European: 61.9%
- East Asian: 36.5%
- African: 1.3%
- Additional Diverse Ancestries: 0.2%
- Publication: Ping J et.al, Int J Cancer (2022-06-29)
- View in PGS-Catalog
Target study
- Coverage: 114 (99.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002744
Reference score
- Variants: 115
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 495,045
- Population:
- European: 61.9%
- East Asian: 36.5%
- African: 1.3%
- Additional Diverse Ancestries: 0.2%
- Publication: Ping J et.al, Int J Cancer (2022-06-29)
- View in PGS-Catalog
Target study
- Coverage: 114 (99.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002745
Reference score
- Variants: 2,575
- Variants ignored: 0
-
Trait: Rheumatoid arthritis
- Mapped Trait(s):
- Samples: 276,020
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Ishigaki K et.al, Nat Genet (2022-11-04)
- View in PGS-Catalog
Target study
- Coverage: 2,575 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002746
Reference score
- Variants: 513,659
- Variants ignored: 0
-
Trait: Attention-deficit hyperactivity disorder
- Mapped Trait(s):
- Samples: 55,374
- Population:
- European: 96.2%
- East Asian: 3.5%
- Unknown: 0.3%
- Publication: Lahey BB et.al, J Psychiatr Res (2022-06-14)
- View in PGS-Catalog
Target study
- Coverage: 513,243 (99.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002747
Reference score
- Variants: 106
- Variants ignored: 0
-
Trait: Gastrointestinal cancer
- Mapped Trait(s):
- Samples: 561,306
- Population:
- Unknown: 58.7%
- European: 41.3%
- Publication: Liu Y et.al, Cancer Med (2022-06-22)
- View in PGS-Catalog
Target study
- Coverage: 103 (97.17%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002748
Reference score
- Variants: 251
- Variants ignored: 64
-
Trait: Height
- Mapped Trait(s):
- Samples: 67,452
- Population:
- Publication: Chiou JS et.al, BMC Med (2022-07-13)
- View in PGS-Catalog
Target study
- Coverage: 177 (70.52%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002749
Reference score
- Variants: 10
- Variants ignored: 1
-
Trait: Total knee replacement
- Mapped Trait(s):
- Samples: 252,041
- Population:
- Publication: Lacaze P et.al, Arthritis Rheumatol (2022-07-23)
- View in PGS-Catalog
Target study
- Coverage: 9 (90%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002750
Reference score
- Variants: 37
- Variants ignored: 7
-
Trait: Total hip replacement
- Mapped Trait(s):
- Samples: 319,037
- Population:
- Publication: Lacaze P et.al, Arthritis Rheumatol (2022-07-23)
- View in PGS-Catalog
Target study
- Coverage: 28 (75.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002751
Reference score
- Variants: 14
- Variants ignored: 0
-
Trait: Body mass index
- Mapped Trait(s):
- Samples: 526,508
- Population:
- European: 85.4%
- South Asian: 5.6%
- African: 5.2%
- Hispanic or Latin American: 2%
- East Asian: 1.7%
- Publication: Sapkota Y et.al, Nat Med (2022-07-25)
- View in PGS-Catalog
Target study
- Coverage: 12 (85.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002752
Reference score
- Variants: 1,089,551
- Variants ignored: 0
-
Trait: Alcohol consumption (drinks per week)
- Mapped Trait(s):
- Samples: 941,280
- Population:
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 1,089,145 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002753
Reference score
- Variants: 1,092,011
- Variants ignored: 0
-
Trait: Alzheimer's disease
- Mapped Trait(s):
- Samples: 455,258
- Population:
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 1,091,603 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002754
Reference score
- Variants: 668,286
- Variants ignored: 0
-
Trait: Asthma
- Mapped Trait(s):
- Samples: 394,283
- Population:
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 668,046 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002755
Reference score
- Variants: 1,090,702
- Variants ignored: 0
-
Trait: Atopic dermatitis
- Mapped Trait(s):
- Samples: 116,863
- Population:
- European: 88.2%
- East Asian: 8.1%
- Hispanic or Latin American: 1.6%
- African: 1.1%
- Unknown: 1%
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 1,090,294 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002756
Reference score
- Variants: 1,091,491
- Variants ignored: 0
-
Trait: Atrial fibrillation
- Mapped Trait(s):
- Samples: 1,030,836
- Population:
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 1,091,092 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002757
Reference score
- Variants: 1,090,783
- Variants ignored: 0
-
Trait: Chronic kidney disease
- Mapped Trait(s):
- Samples: 567,460
- Population:
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 1,090,377 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002758
Reference score
- Variants: 1,087,843
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 106,006
- Population:
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 1,087,439 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002759
Reference score
- Variants: 1,091,613
- Variants ignored: 0
-
Trait: Depression
- Mapped Trait(s):
- Samples: 480,359
- Population:
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 1,091,205 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002760
Reference score
- Variants: 835,537
- Variants ignored: 0
-
Trait: Epilepsy
- Mapped Trait(s):
- Samples: 33,446
- Population:
- European: 83.5%
- East Asian: 8.6%
- African: 7.9%
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 835,340 (99.98%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002761
Reference score
- Variants: 1,082,518
- Variants ignored: 0
-
Trait: Glaucoma
- Mapped Trait(s):
- Samples: 351,696
- Population:
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 1,082,112 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002762
Reference score
- Variants: 1,092,214
- Variants ignored: 0
-
Trait: Gout
- Mapped Trait(s):
- Samples: 457,690
- Population:
- European: 63.1%
- East Asian: 27.5%
- African: 7.4%
- South Asian: 2%
- Hispanic or Latin American: 0.1%
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 1,091,806 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002763
Reference score
- Variants: 1,052,273
- Variants ignored: 0
-
Trait: Hip osteoarthritis
- Mapped Trait(s):
- Samples: 393,873
- Population:
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 1,051,891 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002764
Reference score
- Variants: 1,091,280
- Variants ignored: 0
-
Trait: Hypercholesterolemia
- Mapped Trait(s):
- Samples: 340,951
- Population:
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 1,090,882 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002765
Reference score
- Variants: 1,077,894
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 757,601
- Population:
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 1,077,894 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002766
Reference score
- Variants: 1,092,122
- Variants ignored: 0
-
Trait: Hypothyroidism
- Mapped Trait(s):
- Samples: 406,300
- Population:
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 1,091,714 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002767
Reference score
- Variants: 1,052,275
- Variants ignored: 0
-
Trait: Knee osteoarthritis
- Mapped Trait(s):
- Samples: 403,124
- Population:
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 1,051,894 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002768
Reference score
- Variants: 1,091,549
- Variants ignored: 0
-
Trait: Osteoporosis
- Mapped Trait(s):
- Samples: 394,929
- Population:
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 1,091,148 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002769
Reference score
- Variants: 1,083,565
- Variants ignored: 0
-
Trait: Seropositive rheumatoid arthritis
- Mapped Trait(s):
- Samples: 80,799
- Population:
- European: 72.1%
- East Asian: 27.9%
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 1,083,176 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002770
Reference score
- Variants: 1,088,719
- Variants ignored: 0
-
Trait: Stroke
- Mapped Trait(s):
- Samples: 446,696
- Population:
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 1,088,315 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002771
Reference score
- Variants: 1,091,608
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 898,130
- Population:
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 1,091,606 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002772
Reference score
- Variants: 1,052,790
- Variants ignored: 0
-
Trait: Venous thromboembolism
- Mapped Trait(s):
- Samples: 650,119
- Population:
- European: 88.7%
- African: 7.9%
- Hispanic or Latin American: 3.4%
- Publication: Mars N et.al, Am J Hum Genet (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 1,052,400 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002773
Reference score
- Variants: 265
- Variants ignored: 0
-
Trait: Incident atrial fibrillation
- Mapped Trait(s):
- Samples: 132,118
- Population:
- European: 89.9%
- African: 4.4%
- East Asian: 3.1%
- Hispanic or Latin American: 2.5%
- Publication: Wong CK et.al, PLoS One (2022-12-02)
- View in PGS-Catalog
Target study
- Coverage: 265 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002774
Reference score
- Variants: 216,837
- Variants ignored: 0
-
Trait: Incident atrial fibrillation
- Mapped Trait(s):
- Samples: 132,118
- Population:
- European: 89.9%
- African: 4.4%
- East Asian: 3.1%
- Hispanic or Latin American: 2.5%
- Publication: Wong CK et.al, PLoS One (2022-12-02)
- View in PGS-Catalog
Target study
- Coverage: 216,317 (99.76%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002775
Reference score
- Variants: 1,059
- Variants ignored: 0
-
Trait: Incident coronary artery disease
- Mapped Trait(s):
- Samples: 187,599
- Population:
- European: 75.3%
- South Asian: 13.6%
- East Asian: 6%
- Hispanic or Latin American: 2.2%
- African: 1.7%
- Greater Middle Eastern: 1.2%
- Publication: Wong CK et.al, PLoS One (2022-12-02)
- View in PGS-Catalog
Target study
- Coverage: 1,058 (99.91%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002776
Reference score
- Variants: 390,782
- Variants ignored: 0
-
Trait: Incident coronary artery disease
- Mapped Trait(s):
- Samples: 187,599
- Population:
- European: 75.3%
- South Asian: 13.6%
- East Asian: 6%
- Hispanic or Latin American: 2.2%
- African: 1.7%
- Greater Middle Eastern: 1.2%
- Publication: Wong CK et.al, PLoS One (2022-12-02)
- View in PGS-Catalog
Target study
- Coverage: 389,818 (99.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002777
Reference score
- Variants: 61,669
- Variants ignored: 0
-
Trait: Incident hypertension
- Mapped Trait(s):
- Samples: 458,554
- Population:
- Publication: Wong CK et.al, PLoS One (2022-12-02)
- View in PGS-Catalog
Target study
- Coverage: 61,543 (99.8%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002778
Reference score
- Variants: 309,759
- Variants ignored: 0
-
Trait: Incident hypertension
- Mapped Trait(s):
- Samples: 458,554
- Population:
- Publication: Wong CK et.al, PLoS One (2022-12-02)
- View in PGS-Catalog
Target study
- Coverage: 309,093 (99.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002779
Reference score
- Variants: 46,353
- Variants ignored: 0
-
Trait: Incident type 2 diabetes
- Mapped Trait(s):
- Samples: 159,208
- Population:
- Publication: Wong CK et.al, PLoS One (2022-12-02)
- View in PGS-Catalog
Target study
- Coverage: 46,252 (99.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002780
Reference score
- Variants: 419,209
- Variants ignored: 0
-
Trait: Incident type 2 diabetes
- Mapped Trait(s):
- Samples: 159,208
- Population:
- Publication: Wong CK et.al, PLoS One (2022-12-02)
- View in PGS-Catalog
Target study
- Coverage: 418,116 (99.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002781
Reference score
- Variants: 1,239,184
- Variants ignored: 0
-
Trait: HDL Cholesterol
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 1,654,960
- Population:
- European: 79.8%
- East Asian: 8.9%
- Multi-Ancestry (excluding Europeans): 6%
- Hispanic or Latin American: 2.9%
- South Asian: 2.5%
- Publication: Kanoni S et.al, medRxiv (2021-12-16)
- View in PGS-Catalog
Target study
- Coverage: 1,238,649 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002782
Reference score
- Variants: 1,239,184
- Variants ignored: 0
-
Trait: nonHDL Cholesterol
- Mapped Trait(s):
- EFO_0005689: non-high density lipoprotein cholesterol measurement
- Samples: 1,654,960
- Population:
- European: 79.8%
- East Asian: 8.9%
- Multi-Ancestry (excluding Europeans): 6%
- Hispanic or Latin American: 2.9%
- South Asian: 2.5%
- Publication: Kanoni S et.al, medRxiv (2021-12-16)
- View in PGS-Catalog
Target study
- Coverage: 1,238,649 (99.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002783
Reference score
- Variants: 10,699
- Variants ignored: 0
-
Trait: Total Cholesterol
- Mapped Trait(s):
- Samples: 1,654,960
- Population:
- European: 79.8%
- East Asian: 8.9%
- Multi-Ancestry (excluding Europeans): 6%
- Hispanic or Latin American: 2.9%
- South Asian: 2.5%
- Publication: Kanoni S et.al, medRxiv (2021-12-16)
- View in PGS-Catalog
Target study
- Coverage: 10,672 (99.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002784
Reference score
- Variants: 30,071
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 1,654,960
- Population:
- European: 79.8%
- East Asian: 8.9%
- Multi-Ancestry (excluding Europeans): 6%
- Hispanic or Latin American: 2.9%
- South Asian: 2.5%
- Publication: Kanoni S et.al, medRxiv (2021-12-16)
- View in PGS-Catalog
Target study
- Coverage: 30,011 (99.8%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002785
Reference score
- Variants: 964,422
- Variants ignored: 203,134
-
Trait: Schizophrenia
- Mapped Trait(s):
- Samples: 65,967
- Population:
- Publication: Gui Y et.al, Transl Psychiatry (2022-08-26)
- View in PGS-Catalog
Target study
- Coverage: 761,192 (78.93%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002786
Reference score
- Variants: 948,996
- Variants ignored: 200,442
-
Trait: Bipolar disorder
- Mapped Trait(s):
- Samples: 41,653
- Population:
- Publication: Gui Y et.al, Transl Psychiatry (2022-08-26)
- View in PGS-Catalog
Target study
- Coverage: 748,459 (78.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002787
Reference score
- Variants: 937,511
- Variants ignored: 198,805
-
Trait: Type 1 bipolar disorder
- Mapped Trait(s):
- Samples: 46,237
- Population:
- Publication: Gui Y et.al, Transl Psychiatry (2022-08-26)
- View in PGS-Catalog
Target study
- Coverage: 738,612 (78.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002788
Reference score
- Variants: 935,292
- Variants ignored: 198,365
-
Trait: Type 2 bipolar disorder
- Mapped Trait(s):
- Samples: 34,779
- Population:
- Publication: Gui Y et.al, Transl Psychiatry (2022-08-26)
- View in PGS-Catalog
Target study
- Coverage: 736,835 (78.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002789
Reference score
- Variants: 943,784
- Variants ignored: 197,897
-
Trait: Major depressive disorder
- Mapped Trait(s):
- Samples: 480,359
- Population:
- Publication: Gui Y et.al, Transl Psychiatry (2022-08-26)
- View in PGS-Catalog
Target study
- Coverage: 745,801 (79.02%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002790
Reference score
- Variants: 916,713
- Variants ignored: 194,110
-
Trait: Autism spectrum disorder
- Mapped Trait(s):
- Samples: 46,350
- Population:
- Publication: Gui Y et.al, Transl Psychiatry (2022-08-26)
- View in PGS-Catalog
Target study
- Coverage: 722,513 (78.82%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002791
Reference score
- Variants: 126
- Variants ignored: 21
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 586,244
- Population:
- European: 91.7%
- Multi-Ancestry (including Europeans): 3%
- Unknown: 1.9%
- African: 1.8%
- East Asian: 1.2%
- Hispanic or Latin American: 0.4%
- Publication: Ruan X et.al, Prostate (2022-08-22)
- View in PGS-Catalog
Target study
- Coverage: 105 (83.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002792
Reference score
- Variants: 67
- Variants ignored: 14
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 549,905
- Population:
- European: 91.2%
- Multi-Ancestry (including Europeans): 3.2%
- Unknown: 2.1%
- African: 1.9%
- East Asian: 1.3%
- Hispanic or Latin American: 0.4%
- Publication: Ruan X et.al, Prostate (2022-08-22)
- View in PGS-Catalog
Target study
- Coverage: 53 (79.1%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002793
Reference score
- Variants: 82
- Variants ignored: 19
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 583,410
- Population:
- European: 91.7%
- Multi-Ancestry (including Europeans): 3%
- Unknown: 2%
- African: 1.8%
- East Asian: 1.2%
- Hispanic or Latin American: 0.4%
- Publication: Ruan X et.al, Prostate (2022-08-22)
- View in PGS-Catalog
Target study
- Coverage: 63 (76.83%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002794
Reference score
- Variants: 10
- Variants ignored: 2
-
Trait: Venous thromboembolism
- Mapped Trait(s):
- Samples: 60,139
- Population:
- Publication: Xie J et.al, J Thromb Haemost (2022-09-15)
- View in PGS-Catalog
Target study
- Coverage: 8 (80%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002795
Reference score
- Variants: 4
- Variants ignored: 0
-
Trait: Longevity (>90th survival percentile)
- Mapped Trait(s):
- Samples: 36,745
- Population:
- Publication: Schoepf IC et.al, Clin Infect Dis (2021-11-01)
- View in PGS-Catalog
Target study
- Coverage: 4 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002796
Reference score
- Variants: 232
- Variants ignored: 48
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 583,255
- Population:
- European: 85.4%
- East Asian: 6.4%
- Multi-Ancestry (excluding Europeans): 3.7%
- Hispanic or Latin American: 2.3%
- African: 2.2%
- Publication: Shi Z et.al, Eur Urol Open Sci (2022-09-17)
- View in PGS-Catalog
Target study
- Coverage: 170 (73.28%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002797
Reference score
- Variants: 67
- Variants ignored: 18
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 288,584
- Population:
- European: 74.4%
- East Asian: 10.6%
- Multi-Ancestry (excluding Europeans): 7.4%
- Hispanic or Latin American: 6.8%
- African: 0.8%
- Publication: Shi Z et.al, Eur Urol Open Sci (2022-09-17)
- View in PGS-Catalog
Target study
- Coverage: 45 (67.16%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002798
Reference score
- Variants: 128
- Variants ignored: 31
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 407,351
- Population:
- European: 70.6%
- African: 9.5%
- East Asian: 9.2%
- Multi-Ancestry (excluding Europeans): 7.3%
- Hispanic or Latin American: 3.4%
- Publication: Shi Z et.al, Eur Urol Open Sci (2022-09-17)
- View in PGS-Catalog
Target study
- Coverage: 92 (71.88%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002799
Reference score
- Variants: 138
- Variants ignored: 32
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 306,220
- Population:
- European: 70.1%
- East Asian: 18.4%
- Multi-Ancestry (excluding Europeans): 7%
- Hispanic or Latin American: 3.8%
- African: 0.7%
- Publication: Shi Z et.al, Eur Urol Open Sci (2022-09-17)
- View in PGS-Catalog
Target study
- Coverage: 103 (74.64%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002800
Reference score
- Variants: 1,156,741
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 77,890
- Population:
- Publication: Yengo L et.al, Nature (2022-10-12)
- View in PGS-Catalog
Target study
- Coverage: 1,156,741 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002801
Reference score
- Variants: 975,455
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 293,593
- Population:
- Publication: Yengo L et.al, Nature (2022-10-12)
- View in PGS-Catalog
Target study
- Coverage: 975,455 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002802
Reference score
- Variants: 1,103,042
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 5,314,291
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Yengo L et.al, Nature (2022-10-12)
- View in PGS-Catalog
Target study
- Coverage: 1,100,765 (99.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002803
Reference score
- Variants: 990,792
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 472,730
- Population:
- Publication: Yengo L et.al, Nature (2022-10-12)
- View in PGS-Catalog
Target study
- Coverage: 990,792 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002804
Reference score
- Variants: 1,099,005
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 4,080,687
- Population:
- Publication: Yengo L et.al, Nature (2022-10-12)
- View in PGS-Catalog
Target study
- Coverage: 1,096,728 (99.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002805
Reference score
- Variants: 1,245,514
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 455,180
- Population:
- Hispanic or Latin American: 100%
- Publication: Yengo L et.al, Nature (2022-10-12)
- View in PGS-Catalog
Target study
- Coverage: 1,244,173 (99.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002807
Reference score
- Variants: 1,084,154
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 436,843
- Population:
- European: 95.5%
- Additional Asian Ancestries: 1.9%
- African: 1.5%
- East Asian: 0.6%
- Greater Middle Eastern: 0.3%
- Hispanic or Latin American: 0.2%
- Publication: Parcha V et.al, Circ Genom Precis Med (2022-11-05)
- View in PGS-Catalog
Target study
- Coverage: 1,083,412 (99.93%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002808
Reference score
- Variants: 20
- Variants ignored: 0
-
Trait: Lung cancer
- Mapped Trait(s):
- Samples: 85,716
- Population:
- Publication: Qin N et.al, Lancet Oncol (2022-10-17)
- View in PGS-Catalog
Target study
- Coverage: 20 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002809
Reference score
- Variants: 205
- Variants ignored: 41
-
Trait: Coronary artery disease
- Mapped Trait(s):
- Samples: 2,202,086
- Population:
- Multi-Ancestry (including Europeans): 38.6%
- European: 31.3%
- Unknown: 20.2%
- East Asian: 10%
- Publication: Ahmed R et.al, Int J Cardiol Heart Vasc (2022-10-13)
- View in PGS-Catalog
Target study
- Coverage: 163 (79.51%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002810
Reference score
- Variants: 147
- Variants ignored: 0
-
Trait: Estimated glomerular filtration rate
- Mapped Trait(s):
- Samples: 765,348
- Population:
- European: 74.1%
- East Asian: 21.7%
- African: 1.8%
- South Asian: 1.7%
- Hispanic or Latin American: 0.6%
- Publication: Wuttke M et.al, Nat Genet (2019-05-31)
- View in PGS-Catalog
Target study
- Coverage: 147 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002811
Reference score
- Variants: 1,125,301
- Variants ignored: 0
-
Trait: Abdominal adipose tissue volumes adjusted for BMI and height
- Mapped Trait(s):
- Samples: 37,641
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Agrawal S et.al, Nat Commun (2022-06-30)
- View in PGS-Catalog
Target study
- Coverage: 1,125,301 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002812
Reference score
- Variants: 1,125,301
- Variants ignored: 0
-
Trait: Gluteofemoral adipose tissue volumes adjusted for BMI and height
- Mapped Trait(s):
- Samples: 37,641
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Agrawal S et.al, Nat Commun (2022-06-30)
- View in PGS-Catalog
Target study
- Coverage: 1,125,301 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002813
Reference score
- Variants: 1,125,301
- Variants ignored: 0
-
Trait: Visceral adipose tissue volumes adjusted for BMI and height
- Mapped Trait(s):
- Samples: 37,641
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Agrawal S et.al, Nat Commun (2022-06-30)
- View in PGS-Catalog
Target study
- Coverage: 1,125,301 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002814
Reference score
- Variants: 4,520
- Variants ignored: 0
-
Trait: Atrial fibrillation
- Mapped Trait(s):
- Samples: 1,150,799
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Miyazawa K.M. et.al, Nat Genet (2023-01-19)
- View in PGS-Catalog
Target study
- Coverage: 4,520 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002815
Reference score
- Variants: 137,734
- Variants ignored: 0
-
Trait: Age at Menarche
- Mapped Trait(s):
- Samples: 182,416
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 137,068 (99.52%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002816
Reference score
- Variants: 13,852
- Variants ignored: 0
-
Trait: Age at Menarche
- Mapped Trait(s):
- Samples: 182,416
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 13,598 (98.17%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002817
Reference score
- Variants: 13,852
- Variants ignored: 0
-
Trait: Age at Menarche
- Mapped Trait(s):
- Samples: 182,416
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 13,598 (98.17%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002818
Reference score
- Variants: 991,712
- Variants ignored: 0
-
Trait: Age at Menarche
- Mapped Trait(s):
- Samples: 182,416
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 987,829 (99.61%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002819
Reference score
- Variants: 895,562
- Variants ignored: 0
-
Trait: Age at Menarche
- Mapped Trait(s):
- Samples: 182,416
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 895,562 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002820
Reference score
- Variants: 99,745
- Variants ignored: 0
-
Trait: Age at Menopause
- Mapped Trait(s):
- Samples: 69,360
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 99,295 (99.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002821
Reference score
- Variants: 159
- Variants ignored: 0
-
Trait: Age at Menopause
- Mapped Trait(s):
- Samples: 69,360
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 151 (94.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002822
Reference score
- Variants: 159
- Variants ignored: 0
-
Trait: Age at Menopause
- Mapped Trait(s):
- Samples: 69,360
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 151 (94.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002823
Reference score
- Variants: 1,379,304
- Variants ignored: 0
-
Trait: Age at Menopause
- Mapped Trait(s):
- Samples: 69,360
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,374,002 (99.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002824
Reference score
- Variants: 894,484
- Variants ignored: 0
-
Trait: Age at Menopause
- Mapped Trait(s):
- Samples: 69,360
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 894,484 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002825
Reference score
- Variants: 375,749
- Variants ignored: 0
-
Trait: Alcohol consumption
- Mapped Trait(s):
- Samples: 108,256
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 374,546 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002826
Reference score
- Variants: 19
- Variants ignored: 0
-
Trait: Alcohol consumption
- Mapped Trait(s):
- Samples: 108,256
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 16 (84.21%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002827
Reference score
- Variants: 25
- Variants ignored: 0
-
Trait: Alcohol consumption
- Mapped Trait(s):
- Samples: 108,256
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 24 (96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002828
Reference score
- Variants: 5,498,032
- Variants ignored: 0
-
Trait: Alcohol consumption
- Mapped Trait(s):
- Samples: 108,256
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 5,179,652 (94.21%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002829
Reference score
- Variants: 1,113,829
- Variants ignored: 0
-
Trait: Alcohol consumption
- Mapped Trait(s):
- Samples: 108,256
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,829 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002830
Reference score
- Variants: 524,093
- Variants ignored: 0
-
Trait: Alcohol consumption
- Mapped Trait(s):
- Samples: 941,280
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 522,170 (99.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002831
Reference score
- Variants: 12,650
- Variants ignored: 0
-
Trait: Alcohol consumption
- Mapped Trait(s):
- Samples: 941,280
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 12,514 (98.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002832
Reference score
- Variants: 27,085
- Variants ignored: 0
-
Trait: Alcohol consumption
- Mapped Trait(s):
- Samples: 941,280
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 24,218 (89.41%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002833
Reference score
- Variants: 232
- Variants ignored: 0
-
Trait: Alcohol consumption
- Mapped Trait(s):
- Samples: 941,280
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 218 (93.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002834
Reference score
- Variants: 1,116,497
- Variants ignored: 0
-
Trait: Alcohol consumption
- Mapped Trait(s):
- Samples: 941,280
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,116,497 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002835
Reference score
- Variants: 524,875
- Variants ignored: 0
-
Trait: Alcohol consumption
- Mapped Trait(s):
- Samples: 941,280
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 522,821 (99.61%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002836
Reference score
- Variants: 10,706
- Variants ignored: 0
-
Trait: Alcohol consumption
- Mapped Trait(s):
- Samples: 941,280
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 10,581 (98.83%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002837
Reference score
- Variants: 22,675
- Variants ignored: 0
-
Trait: Alcohol consumption
- Mapped Trait(s):
- Samples: 941,280
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 20,279 (89.43%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002838
Reference score
- Variants: 137
- Variants ignored: 0
-
Trait: Alcohol consumption
- Mapped Trait(s):
- Samples: 941,280
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 133 (97.08%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002839
Reference score
- Variants: 1,117,376
- Variants ignored: 0
-
Trait: Alcohol consumption
- Mapped Trait(s):
- Samples: 941,280
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,117,376 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002840
Reference score
- Variants: 1,062,550
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 359,983
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,059,231 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002841
Reference score
- Variants: 32,980
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 359,983
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 32,063 (97.22%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002842
Reference score
- Variants: 51,983
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 359,983
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 47,634 (91.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002843
Reference score
- Variants: 7,444,639
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 359,983
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,008,700 (94.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002844
Reference score
- Variants: 1,113,832
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 359,983
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,832 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002845
Reference score
- Variants: 1,052,511
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 359,983
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,049,203 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002846
Reference score
- Variants: 32,526
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 359,983
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 31,604 (97.17%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002847
Reference score
- Variants: 51,370
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 359,983
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 47,034 (91.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002848
Reference score
- Variants: 7,444,629
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 359,983
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,008,688 (94.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002849
Reference score
- Variants: 1,113,832
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 359,983
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,832 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002850
Reference score
- Variants: 1,053,861
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 354,831
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,050,563 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002851
Reference score
- Variants: 32,697
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 354,831
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 31,785 (97.21%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002852
Reference score
- Variants: 51,563
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 354,831
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 47,274 (91.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002853
Reference score
- Variants: 7,446,664
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 354,831
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,010,770 (94.15%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002854
Reference score
- Variants: 1,113,832
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 354,831
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,832 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002855
Reference score
- Variants: 1,044,654
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 354,831
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,041,387 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002856
Reference score
- Variants: 28,689
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 354,831
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 27,879 (97.18%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002857
Reference score
- Variants: 44,240
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 354,831
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 40,694 (91.98%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002858
Reference score
- Variants: 7,446,652
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 354,831
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,010,758 (94.15%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002859
Reference score
- Variants: 1,113,832
- Variants ignored: 0
-
Trait: BMI
- Mapped Trait(s):
- Samples: 354,831
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,832 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002860
Reference score
- Variants: 579,046
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 9,541
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 573,783 (99.09%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002861
Reference score
- Variants: 414,578
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 9,541
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 265,524 (64.05%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002862
Reference score
- Variants: 407,315
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 9,541
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 265,524 (65.19%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002863
Reference score
- Variants: 1,118,117
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 9,541
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,118,117 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002864
Reference score
- Variants: 763,400
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 343,524
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 761,019 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002865
Reference score
- Variants: 9,373
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 343,524
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 9,129 (97.4%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002866
Reference score
- Variants: 13,371
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 343,524
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 12,503 (93.51%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002867
Reference score
- Variants: 10,306,310
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 343,524
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 9,777,032 (94.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002868
Reference score
- Variants: 1,113,831
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 343,524
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,831 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002869
Reference score
- Variants: 481,279
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 343,524
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 479,778 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002870
Reference score
- Variants: 630
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 343,524
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 618 (98.1%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002871
Reference score
- Variants: 837
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 343,524
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 786 (93.91%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002872
Reference score
- Variants: 10,306,271
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 343,524
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 9,776,993 (94.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002873
Reference score
- Variants: 1,113,831
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 343,524
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,831 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002874
Reference score
- Variants: 316,203
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 3,301
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 315,462 (99.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002875
Reference score
- Variants: 5
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 3,301
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 5 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002876
Reference score
- Variants: 5
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 3,301
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 5 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002877
Reference score
- Variants: 1,662,602
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 3,301
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,655,066 (99.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002878
Reference score
- Variants: 1,113,794
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 3,301
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,794 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002879
Reference score
- Variants: 721,243
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 9,541
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 711,622 (98.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002880
Reference score
- Variants: 2
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 9,541
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002881
Reference score
- Variants: 2
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 9,541
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002882
Reference score
- Variants: 746
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 9,541
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 664 (89.01%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002883
Reference score
- Variants: 1,119,064
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 9,541
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,119,064 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002884
Reference score
- Variants: 370,520
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 3,301
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 367,232 (99.11%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002885
Reference score
- Variants: 5
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 3,301
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 4 (80%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002886
Reference score
- Variants: 5
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 3,301
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 4 (80%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002887
Reference score
- Variants: 444,857
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 3,301
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 439,362 (98.76%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002888
Reference score
- Variants: 1,114,754
- Variants ignored: 0
-
Trait: C-reactive Protein
- Mapped Trait(s):
- Samples: 3,301
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,114,754 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002889
Reference score
- Variants: 755,822
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 340,162
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 753,375 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002890
Reference score
- Variants: 24,016
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 340,162
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 23,310 (97.06%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002891
Reference score
- Variants: 40,911
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 340,162
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 37,060 (90.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002892
Reference score
- Variants: 7,477,069
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 340,162
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,040,257 (94.16%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002893
Reference score
- Variants: 1,113,831
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 340,162
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,831 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002894
Reference score
- Variants: 749,859
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 340,162
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 747,419 (99.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002895
Reference score
- Variants: 15,687
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 340,162
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 15,249 (97.21%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002896
Reference score
- Variants: 24,976
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 340,162
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 22,852 (91.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002897
Reference score
- Variants: 7,259,551
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 340,162
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 6,835,058 (94.15%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002898
Reference score
- Variants: 1,113,831
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 340,162
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,831 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002899
Reference score
- Variants: 353,663
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 31,281
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 352,601 (99.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002900
Reference score
- Variants: 13,289
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 31,281
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 12,909 (97.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002901
Reference score
- Variants: 27,506
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 31,281
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 24,433 (88.83%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002902
Reference score
- Variants: 7,218,263
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 31,281
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 6,820,706 (94.49%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002903
Reference score
- Variants: 1,113,774
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 31,281
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,774 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002904
Reference score
- Variants: 353,446
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 31,281
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 352,396 (99.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002905
Reference score
- Variants: 10,968
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 31,281
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 10,649 (97.09%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002906
Reference score
- Variants: 22,461
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 31,281
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 19,939 (88.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002907
Reference score
- Variants: 6,683,891
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 31,281
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 6,316,767 (94.51%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002908
Reference score
- Variants: 1,113,774
- Variants ignored: 0
-
Trait: Diastolic Blood Pressure
- Mapped Trait(s):
- Samples: 31,281
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,774 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002909
Reference score
- Variants: 396,976
- Variants ignored: 0
-
Trait: Drinking Status
- Mapped Trait(s):
- Samples: 360,726
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 395,762 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002910
Reference score
- Variants: 10,123
- Variants ignored: 0
-
Trait: Drinking Status
- Mapped Trait(s):
- Samples: 360,726
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 9,879 (97.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002911
Reference score
- Variants: 20,050
- Variants ignored: 0
-
Trait: Drinking Status
- Mapped Trait(s):
- Samples: 360,726
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 17,791 (88.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002912
Reference score
- Variants: 8,598,752
- Variants ignored: 0
-
Trait: Drinking Status
- Mapped Trait(s):
- Samples: 360,726
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 8,158,445 (94.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002913
Reference score
- Variants: 1,113,832
- Variants ignored: 0
-
Trait: Drinking Status
- Mapped Trait(s):
- Samples: 360,726
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,832 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002914
Reference score
- Variants: 326,223
- Variants ignored: 0
-
Trait: Estradiol
- Mapped Trait(s):
- Samples: 54,498
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 325,305 (99.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002915
Reference score
- Variants: 4,661
- Variants ignored: 0
-
Trait: Estradiol
- Mapped Trait(s):
- Samples: 54,498
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 4,558 (97.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002916
Reference score
- Variants: 9,583
- Variants ignored: 0
-
Trait: Estradiol
- Mapped Trait(s):
- Samples: 54,498
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 8,516 (88.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002917
Reference score
- Variants: 10,287,664
- Variants ignored: 0
-
Trait: Estradiol
- Mapped Trait(s):
- Samples: 54,498
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 9,767,933 (94.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002918
Reference score
- Variants: 1,113,823
- Variants ignored: 0
-
Trait: Estradiol
- Mapped Trait(s):
- Samples: 54,498
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,823 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002919
Reference score
- Variants: 324,623
- Variants ignored: 0
-
Trait: Estradiol
- Mapped Trait(s):
- Samples: 54,498
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 323,659 (99.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002920
Reference score
- Variants: 4
- Variants ignored: 0
-
Trait: Estradiol
- Mapped Trait(s):
- Samples: 54,498
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 4 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002921
Reference score
- Variants: 98
- Variants ignored: 0
-
Trait: Estradiol
- Mapped Trait(s):
- Samples: 54,498
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 68 (69.39%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002922
Reference score
- Variants: 10,287,670
- Variants ignored: 0
-
Trait: Estradiol
- Mapped Trait(s):
- Samples: 54,498
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 9,767,935 (94.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002923
Reference score
- Variants: 1,113,823
- Variants ignored: 0
-
Trait: Estradiol
- Mapped Trait(s):
- Samples: 54,498
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,823 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002924
Reference score
- Variants: 281
- Variants ignored: 0
-
Trait: Fasting Plasma Glucose
- Mapped Trait(s):
- Samples: 13,807
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 219 (77.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002925
Reference score
- Variants: 13
- Variants ignored: 0
-
Trait: Fasting Plasma Glucose
- Mapped Trait(s):
- Samples: 13,807
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 8 (61.54%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002926
Reference score
- Variants: 13
- Variants ignored: 0
-
Trait: Fasting Plasma Glucose
- Mapped Trait(s):
- Samples: 13,807
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 8 (61.54%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002927
Reference score
- Variants: 5,106
- Variants ignored: 0
-
Trait: Fasting Plasma Glucose
- Mapped Trait(s):
- Samples: 13,807
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 3,783 (74.09%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002928
Reference score
- Variants: 392
- Variants ignored: 0
-
Trait: Fasting Plasma Glucose
- Mapped Trait(s):
- Samples: 13,807
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 392 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002929
Reference score
- Variants: 71,791
- Variants ignored: 0
-
Trait: Fasting Plasma Glucose
- Mapped Trait(s):
- Samples: 46,186
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 71,487 (99.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002930
Reference score
- Variants: 264
- Variants ignored: 0
-
Trait: Fasting Plasma Glucose
- Mapped Trait(s):
- Samples: 46,186
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 263 (99.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002931
Reference score
- Variants: 273
- Variants ignored: 0
-
Trait: Fasting Plasma Glucose
- Mapped Trait(s):
- Samples: 46,186
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 272 (99.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002932
Reference score
- Variants: 1,202,298
- Variants ignored: 0
-
Trait: Fasting Plasma Glucose
- Mapped Trait(s):
- Samples: 46,186
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,198,196 (99.66%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002933
Reference score
- Variants: 1,007,415
- Variants ignored: 0
-
Trait: Fasting Plasma Glucose
- Mapped Trait(s):
- Samples: 46,186
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,007,415 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002934
Reference score
- Variants: 513,495
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 314,916
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 511,858 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002935
Reference score
- Variants: 4,535
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 314,916
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 4,379 (96.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002936
Reference score
- Variants: 4,405
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 314,916
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 4,384 (99.52%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002937
Reference score
- Variants: 7,600,988
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 314,916
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,576,778 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002938
Reference score
- Variants: 1,113,830
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 314,916
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,830 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002939
Reference score
- Variants: 444,825
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 314,916
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 443,411 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002940
Reference score
- Variants: 1,080
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 314,916
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,033 (95.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002941
Reference score
- Variants: 1,049
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 314,916
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,038 (98.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002942
Reference score
- Variants: 7,600,988
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 314,916
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,576,778 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002943
Reference score
- Variants: 1,113,830
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 314,916
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,830 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002944
Reference score
- Variants: 519
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 13,807
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 359 (69.17%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002945
Reference score
- Variants: 1,479
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 13,807
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 933 (63.08%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002946
Reference score
- Variants: 1,553
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 13,807
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 970 (62.46%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002947
Reference score
- Variants: 1,501
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 13,807
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 975 (64.96%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002948
Reference score
- Variants: 392
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 13,807
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 392 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002949
Reference score
- Variants: 72,352
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 46,186
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 72,035 (99.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002950
Reference score
- Variants: 38
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 46,186
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 38 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002951
Reference score
- Variants: 38
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 46,186
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 38 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002952
Reference score
- Variants: 1,501
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 46,186
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 975 (64.96%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002953
Reference score
- Variants: 1,008,035
- Variants ignored: 0
-
Trait: Glucose
- Mapped Trait(s):
- Samples: 46,186
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,008,035 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002954
Reference score
- Variants: 815,573
- Variants ignored: 0
-
Trait: HDL
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 315,133
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 812,975 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002955
Reference score
- Variants: 16,393
- Variants ignored: 0
-
Trait: HDL
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 315,133
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 15,924 (97.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002956
Reference score
- Variants: 25,134
- Variants ignored: 0
-
Trait: HDL
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 315,133
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 23,114 (91.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002957
Reference score
- Variants: 7,449,065
- Variants ignored: 0
-
Trait: HDL
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 315,133
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,013,207 (94.15%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002958
Reference score
- Variants: 1,113,830
- Variants ignored: 0
-
Trait: HDL
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 315,133
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,830 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002959
Reference score
- Variants: 799,981
- Variants ignored: 0
-
Trait: HDL
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 315,133
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 797,480 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002960
Reference score
- Variants: 17,935
- Variants ignored: 0
-
Trait: HDL
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 315,133
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 17,475 (97.44%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002961
Reference score
- Variants: 28,354
- Variants ignored: 0
-
Trait: HDL
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 315,133
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 25,974 (91.61%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002962
Reference score
- Variants: 7,449,036
- Variants ignored: 0
-
Trait: HDL
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 315,133
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,013,179 (94.15%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002963
Reference score
- Variants: 1,113,830
- Variants ignored: 0
-
Trait: HDL
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 315,133
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,830 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002964
Reference score
- Variants: 1,291,379
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 360,388
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,287,228 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002965
Reference score
- Variants: 34,284
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 360,388
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 33,171 (96.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002966
Reference score
- Variants: 49,307
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 360,388
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 45,835 (92.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002967
Reference score
- Variants: 10,297,259
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 360,388
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 9,768,406 (94.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002968
Reference score
- Variants: 1,113,832
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 360,388
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,832 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002969
Reference score
- Variants: 1,296,068
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 360,388
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,291,910 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002970
Reference score
- Variants: 31,805
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 360,388
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 30,720 (96.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002971
Reference score
- Variants: 44,500
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 360,388
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 41,563 (93.4%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002972
Reference score
- Variants: 10,297,262
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 360,388
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 9,768,409 (94.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002973
Reference score
- Variants: 1,113,832
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 360,388
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,832 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002974
Reference score
- Variants: 66,842
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 133,154
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 66,607 (99.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002975
Reference score
- Variants: 22,154
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 133,154
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 22,053 (99.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002976
Reference score
- Variants: 22,443
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 133,154
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 22,341 (99.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002977
Reference score
- Variants: 1,851,736
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 133,154
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,845,168 (99.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002978
Reference score
- Variants: 996,356
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 133,154
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 996,356 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002979
Reference score
- Variants: 280,347
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 253,288
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 279,189 (99.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002980
Reference score
- Variants: 2,469
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 253,288
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,401 (97.25%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002981
Reference score
- Variants: 2,500
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 253,288
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,432 (97.28%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002982
Reference score
- Variants: 912,901
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 253,288
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 909,790 (99.66%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002983
Reference score
- Variants: 915,020
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 253,288
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 915,020 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002984
Reference score
- Variants: 67,333
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 133,154
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 67,083 (99.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002985
Reference score
- Variants: 31,267
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 133,154
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 31,101 (99.47%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002986
Reference score
- Variants: 31,700
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 133,154
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 31,532 (99.47%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002987
Reference score
- Variants: 1,661,426
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 133,154
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,655,729 (99.66%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002988
Reference score
- Variants: 996,840
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 133,154
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 996,840 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002989
Reference score
- Variants: 282,132
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 253,288
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 280,874 (99.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002990
Reference score
- Variants: 6,903
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 253,288
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 6,754 (97.84%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002991
Reference score
- Variants: 7,080
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 253,288
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 6,926 (97.82%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002992
Reference score
- Variants: 464,103
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 253,288
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 462,343 (99.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002993
Reference score
- Variants: 915,553
- Variants ignored: 0
-
Trait: Height
- Mapped Trait(s):
- Samples: 253,288
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 915,553 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002994
Reference score
- Variants: 724,579
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 722,297 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002995
Reference score
- Variants: 26,671
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 25,788 (96.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002996
Reference score
- Variants: 25,909
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 25,788 (99.53%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002997
Reference score
- Variants: 7,601,215
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,577,007 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002998
Reference score
- Variants: 1,113,832
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,832 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS002999
Reference score
- Variants: 313,080
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 312,137 (99.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003000
Reference score
- Variants: 83,829
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 80,845 (96.44%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003001
Reference score
- Variants: 81,218
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 80,848 (99.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003002
Reference score
- Variants: 7,601,215
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,577,007 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003003
Reference score
- Variants: 1,109,030
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 361,141
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,109,030 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003004
Reference score
- Variants: 4,943
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 166,552
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 4,572 (92.49%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003005
Reference score
- Variants: 2,860
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 166,552
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,207 (77.17%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003006
Reference score
- Variants: 5,212
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 166,552
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 3,907 (74.96%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003007
Reference score
- Variants: 359
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 166,552
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 295 (82.17%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003008
Reference score
- Variants: 12,076
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 166,552
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 12,076 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003009
Reference score
- Variants: 5,226
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 176,868
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 4,801 (91.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003010
Reference score
- Variants: 1,894
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 176,868
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,454 (76.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003011
Reference score
- Variants: 3,300
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 176,868
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,493 (75.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003012
Reference score
- Variants: 361
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 176,868
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 295 (81.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003013
Reference score
- Variants: 12,076
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 176,868
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 12,076 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003014
Reference score
- Variants: 294,142
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 293,270 (99.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003015
Reference score
- Variants: 58,725
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 56,738 (96.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003016
Reference score
- Variants: 56,978
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 56,743 (99.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003017
Reference score
- Variants: 7,094,727
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,072,097 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003018
Reference score
- Variants: 1,096,197
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 361,194
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,096,197 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003019
Reference score
- Variants: 6,731
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 166,552
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 5,792 (86.05%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003020
Reference score
- Variants: 24
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 166,552
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 14 (58.33%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003021
Reference score
- Variants: 24
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 166,552
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 14 (58.33%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003022
Reference score
- Variants: 56
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 166,552
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 36 (64.29%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003023
Reference score
- Variants: 12,097
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 166,552
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 12,097 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003024
Reference score
- Variants: 7,123
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 176,868
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 6,069 (85.2%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003025
Reference score
- Variants: 9
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 176,868
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 6 (66.67%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003026
Reference score
- Variants: 9
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 176,868
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 6 (66.67%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003027
Reference score
- Variants: 59
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 176,868
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 40 (67.8%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003028
Reference score
- Variants: 12,097
- Variants ignored: 0
-
Trait: Hypertension
- Mapped Trait(s):
- Samples: 176,868
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 12,097 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003029
Reference score
- Variants: 549,112
- Variants ignored: 0
-
Trait: LDL
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 343,621
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 547,346 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003030
Reference score
- Variants: 2,066
- Variants ignored: 0
-
Trait: LDL
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 343,621
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,033 (98.4%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003031
Reference score
- Variants: 2,609
- Variants ignored: 0
-
Trait: LDL
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 343,621
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,467 (94.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003032
Reference score
- Variants: 7,457,930
- Variants ignored: 0
-
Trait: LDL
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 343,621
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,021,084 (94.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003033
Reference score
- Variants: 1,113,830
- Variants ignored: 0
-
Trait: LDL
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 343,621
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,830 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003034
Reference score
- Variants: 552,845
- Variants ignored: 0
-
Trait: LDL
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 343,621
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 551,078 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003035
Reference score
- Variants: 2,288
- Variants ignored: 0
-
Trait: LDL
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 343,621
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,252 (98.43%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003036
Reference score
- Variants: 2,935
- Variants ignored: 0
-
Trait: LDL
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 343,621
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,780 (94.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003037
Reference score
- Variants: 8,918,470
- Variants ignored: 0
-
Trait: LDL
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 343,621
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 8,394,859 (94.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003038
Reference score
- Variants: 1,113,830
- Variants ignored: 0
-
Trait: LDL
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 343,621
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,830 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003039
Reference score
- Variants: 378,933
- Variants ignored: 0
-
Trait: Polyunsatturated Fatty Acids
- Mapped Trait(s):
- Samples: 13,549
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 374,590 (98.85%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003040
Reference score
- Variants: 13
- Variants ignored: 0
-
Trait: Polyunsatturated Fatty Acids
- Mapped Trait(s):
- Samples: 13,549
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 13 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003041
Reference score
- Variants: 13
- Variants ignored: 0
-
Trait: Polyunsatturated Fatty Acids
- Mapped Trait(s):
- Samples: 13,549
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 13 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003042
Reference score
- Variants: 272
- Variants ignored: 0
-
Trait: Polyunsatturated Fatty Acids
- Mapped Trait(s):
- Samples: 13,549
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 265 (97.43%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003043
Reference score
- Variants: 1,116,151
- Variants ignored: 0
-
Trait: Polyunsatturated Fatty Acids
- Mapped Trait(s):
- Samples: 13,549
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,116,151 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003044
Reference score
- Variants: 520,707
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 359,706
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 519,127 (99.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003045
Reference score
- Variants: 14,682
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 359,706
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 14,178 (96.57%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003046
Reference score
- Variants: 27,004
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 359,706
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 24,168 (89.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003047
Reference score
- Variants: 7,075,957
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 359,706
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 6,660,380 (94.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003048
Reference score
- Variants: 1,113,832
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 359,706
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,832 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003049
Reference score
- Variants: 515,021
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 359,706
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 513,482 (99.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003050
Reference score
- Variants: 1,485
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 359,706
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,425 (95.96%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003051
Reference score
- Variants: 2,146
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 359,706
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,998 (93.1%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003052
Reference score
- Variants: 6,575,783
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 359,706
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 6,187,687 (94.1%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003053
Reference score
- Variants: 1,113,832
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 359,706
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,832 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003054
Reference score
- Variants: 595,975
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 359,751
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 594,138 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003055
Reference score
- Variants: 8,787
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 359,751
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 8,485 (96.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003056
Reference score
- Variants: 14,184
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 359,751
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 12,891 (90.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003057
Reference score
- Variants: 7,433,494
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 359,751
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 6,998,439 (94.15%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003058
Reference score
- Variants: 1,113,832
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 359,751
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,832 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003059
Reference score
- Variants: 641,463
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 1,232,091
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 639,446 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003060
Reference score
- Variants: 8,148
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 1,232,091
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 8,100 (99.41%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003061
Reference score
- Variants: 15,848
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 1,232,091
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 14,692 (92.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003062
Reference score
- Variants: 355
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 1,232,091
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 340 (95.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003063
Reference score
- Variants: 1,109,786
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 1,232,091
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,109,786 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003064
Reference score
- Variants: 642,068
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 1,232,091
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 639,969 (99.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003065
Reference score
- Variants: 17,138
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 1,232,091
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 16,964 (98.98%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003066
Reference score
- Variants: 39,469
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 1,232,091
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 35,827 (90.77%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003067
Reference score
- Variants: 244
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 1,232,091
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 239 (97.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003068
Reference score
- Variants: 1,110,662
- Variants ignored: 0
-
Trait: Smoking Status
- Mapped Trait(s):
- Samples: 1,232,091
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,110,662 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003069
Reference score
- Variants: 775,138
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 340,159
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 772,574 (99.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003070
Reference score
- Variants: 24,765
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 340,159
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 24,044 (97.09%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003071
Reference score
- Variants: 41,867
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 340,159
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 37,914 (90.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003072
Reference score
- Variants: 7,477,086
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 340,159
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,040,274 (94.16%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003073
Reference score
- Variants: 1,113,831
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 340,159
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,831 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003074
Reference score
- Variants: 730,914
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 340,159
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 728,482 (99.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003075
Reference score
- Variants: 16,283
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 340,159
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 15,821 (97.16%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003076
Reference score
- Variants: 25,673
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 340,159
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 23,542 (91.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003077
Reference score
- Variants: 7,477,072
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 340,159
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,040,260 (94.16%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003078
Reference score
- Variants: 1,113,831
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 340,159
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,831 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003079
Reference score
- Variants: 354,112
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 31,281
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 353,059 (99.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003080
Reference score
- Variants: 11,085
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 31,281
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 10,760 (97.07%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003081
Reference score
- Variants: 22,519
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 31,281
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 20,049 (89.03%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003082
Reference score
- Variants: 6,341,932
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 31,281
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 5,993,525 (94.51%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003083
Reference score
- Variants: 1,113,774
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 31,281
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,774 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003084
Reference score
- Variants: 353,555
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 31,281
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 352,478 (99.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003085
Reference score
- Variants: 13,447
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 31,281
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 13,027 (96.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003086
Reference score
- Variants: 27,471
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 31,281
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 24,425 (88.91%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003087
Reference score
- Variants: 6,762,103
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 31,281
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 6,389,777 (94.49%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003088
Reference score
- Variants: 1,113,774
- Variants ignored: 0
-
Trait: Systolic Blood Pressure
- Mapped Trait(s):
- Samples: 31,281
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,774 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003089
Reference score
- Variants: 488,969
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 360,192
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 487,442 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003090
Reference score
- Variants: 1,888
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 360,192
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,780 (94.28%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003091
Reference score
- Variants: 2,707
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 360,192
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,504 (92.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003092
Reference score
- Variants: 10,304,000
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 360,192
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 9,774,736 (94.86%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003093
Reference score
- Variants: 1,113,832
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 360,192
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,832 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003094
Reference score
- Variants: 266,890
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 70,127
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 265,739 (99.57%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003095
Reference score
- Variants: 45
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 70,127
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 44 (97.78%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003096
Reference score
- Variants: 46
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 70,127
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 45 (97.83%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003097
Reference score
- Variants: 229
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 70,127
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 222 (96.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003098
Reference score
- Variants: 1,116,101
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 70,127
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,116,101 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003099
Reference score
- Variants: 555,512
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 61,714
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 554,050 (99.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003100
Reference score
- Variants: 5,693
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 61,714
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 5,681 (99.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003101
Reference score
- Variants: 5,693
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 61,714
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 5,681 (99.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003102
Reference score
- Variants: 5,052,574
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 61,714
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 5,039,140 (99.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003103
Reference score
- Variants: 945,820
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 61,714
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 945,820 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003104
Reference score
- Variants: 374,510
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 159,208
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 370,913 (99.04%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003105
Reference score
- Variants: 187
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 159,208
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 184 (98.4%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003106
Reference score
- Variants: 187
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 159,208
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 184 (98.4%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003107
Reference score
- Variants: 995
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 159,208
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 978 (98.29%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003108
Reference score
- Variants: 1,118,480
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 159,208
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,118,480 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003109
Reference score
- Variants: 311,565
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 70,127
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 306,707 (98.44%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003110
Reference score
- Variants: 118
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 70,127
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 111 (94.07%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003111
Reference score
- Variants: 143
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 70,127
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 132 (92.31%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003112
Reference score
- Variants: 222
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 70,127
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 211 (95.05%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003113
Reference score
- Variants: 1,117,087
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 70,127
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,117,087 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003114
Reference score
- Variants: 555,528
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 61,714
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 554,066 (99.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003115
Reference score
- Variants: 31,462
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 61,714
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 31,386 (99.76%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003116
Reference score
- Variants: 31,462
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 61,714
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 31,386 (99.76%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003117
Reference score
- Variants: 5,052,993
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 61,714
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 5,039,557 (99.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003118
Reference score
- Variants: 945,921
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 61,714
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 945,921 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003119
Reference score
- Variants: 407,553
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 159,208
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 400,163 (98.19%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003120
Reference score
- Variants: 193
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 159,208
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 190 (98.45%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003121
Reference score
- Variants: 193
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 159,208
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 190 (98.45%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003122
Reference score
- Variants: 264
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 159,208
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 260 (98.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003123
Reference score
- Variants: 1,119,522
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 159,208
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,119,522 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003124
Reference score
- Variants: 224,595
- Variants ignored: 0
-
Trait: Thinness
- Mapped Trait(s):
- Samples: 9,203
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 223,956 (99.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003125
Reference score
- Variants: 256
- Variants ignored: 0
-
Trait: Thinness
- Mapped Trait(s):
- Samples: 9,203
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 254 (99.22%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003126
Reference score
- Variants: 351
- Variants ignored: 0
-
Trait: Thinness
- Mapped Trait(s):
- Samples: 9,203
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 348 (99.15%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003127
Reference score
- Variants: 344,981
- Variants ignored: 0
-
Trait: Thinness
- Mapped Trait(s):
- Samples: 9,203
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 343,193 (99.48%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003128
Reference score
- Variants: 1,116,425
- Variants ignored: 0
-
Trait: Thinness
- Mapped Trait(s):
- Samples: 9,203
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,116,425 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003129
Reference score
- Variants: 281,336
- Variants ignored: 0
-
Trait: Thinness
- Mapped Trait(s):
- Samples: 9,203
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 276,810 (98.39%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003130
Reference score
- Variants: 4,280
- Variants ignored: 0
-
Trait: Thinness
- Mapped Trait(s):
- Samples: 9,203
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 4,141 (96.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003131
Reference score
- Variants: 5,164
- Variants ignored: 0
-
Trait: Thinness
- Mapped Trait(s):
- Samples: 9,203
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 5,014 (97.1%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003132
Reference score
- Variants: 41,698
- Variants ignored: 0
-
Trait: Thinness
- Mapped Trait(s):
- Samples: 9,203
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 41,139 (98.66%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003133
Reference score
- Variants: 1,117,469
- Variants ignored: 0
-
Trait: Thinness
- Mapped Trait(s):
- Samples: 9,203
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,117,469 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003134
Reference score
- Variants: 585,328
- Variants ignored: 0
-
Trait: Total Cholesterol
- Mapped Trait(s):
- Samples: 344,278
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 583,480 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003135
Reference score
- Variants: 2,822
- Variants ignored: 0
-
Trait: Total Cholesterol
- Mapped Trait(s):
- Samples: 344,278
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,778 (98.44%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003136
Reference score
- Variants: 3,566
- Variants ignored: 0
-
Trait: Total Cholesterol
- Mapped Trait(s):
- Samples: 344,278
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 3,392 (95.12%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003137
Reference score
- Variants: 7,459,292
- Variants ignored: 0
-
Trait: Total Cholesterol
- Mapped Trait(s):
- Samples: 344,278
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,022,458 (94.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003138
Reference score
- Variants: 1,113,831
- Variants ignored: 0
-
Trait: Total Cholesterol
- Mapped Trait(s):
- Samples: 344,278
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,831 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003139
Reference score
- Variants: 569,518
- Variants ignored: 0
-
Trait: Total Cholesterol
- Mapped Trait(s):
- Samples: 344,278
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 567,712 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003140
Reference score
- Variants: 2,863
- Variants ignored: 0
-
Trait: Total Cholesterol
- Mapped Trait(s):
- Samples: 344,278
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,820 (98.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003141
Reference score
- Variants: 3,604
- Variants ignored: 0
-
Trait: Total Cholesterol
- Mapped Trait(s):
- Samples: 344,278
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 3,436 (95.34%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003142
Reference score
- Variants: 7,459,288
- Variants ignored: 0
-
Trait: Total Cholesterol
- Mapped Trait(s):
- Samples: 344,278
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,022,455 (94.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003143
Reference score
- Variants: 1,113,831
- Variants ignored: 0
-
Trait: Total Cholesterol
- Mapped Trait(s):
- Samples: 344,278
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,831 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003144
Reference score
- Variants: 762,608
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 343,992
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 760,235 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003145
Reference score
- Variants: 9,693
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 343,992
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 9,399 (96.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003146
Reference score
- Variants: 13,680
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 343,992
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 12,758 (93.26%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003147
Reference score
- Variants: 8,924,773
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 343,992
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 8,400,781 (94.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003148
Reference score
- Variants: 1,113,831
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 343,992
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,831 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003149
Reference score
- Variants: 705,677
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 343,992
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 703,424 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003150
Reference score
- Variants: 5,113
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 343,992
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 4,918 (96.19%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003151
Reference score
- Variants: 6,730
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 343,992
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 6,342 (94.23%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003152
Reference score
- Variants: 8,924,752
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 343,992
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 8,400,761 (94.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003153
Reference score
- Variants: 1,113,831
- Variants ignored: 0
-
Trait: Triglycerides
- Mapped Trait(s):
- Samples: 343,992
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,831 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003154
Reference score
- Variants: 314,838
- Variants ignored: 0
-
Trait: Vitamin B12
- Mapped Trait(s):
- Samples: 51,453
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 313,865 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003155
Reference score
- Variants: 40,176
- Variants ignored: 0
-
Trait: Vitamin B12
- Mapped Trait(s):
- Samples: 51,453
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 38,723 (96.38%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003156
Reference score
- Variants: 88,908
- Variants ignored: 0
-
Trait: Vitamin B12
- Mapped Trait(s):
- Samples: 51,453
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 77,608 (87.29%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003157
Reference score
- Variants: 10,318,270
- Variants ignored: 0
-
Trait: Vitamin B12
- Mapped Trait(s):
- Samples: 51,453
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 9,801,274 (94.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003158
Reference score
- Variants: 1,113,819
- Variants ignored: 0
-
Trait: Vitamin B12
- Mapped Trait(s):
- Samples: 51,453
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,819 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003159
Reference score
- Variants: 313,902
- Variants ignored: 0
-
Trait: Vitamin B12
- Mapped Trait(s):
- Samples: 51,453
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 312,879 (99.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003160
Reference score
- Variants: 83,714
- Variants ignored: 0
-
Trait: Vitamin B12
- Mapped Trait(s):
- Samples: 51,453
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 80,574 (96.25%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003161
Reference score
- Variants: 190,297
- Variants ignored: 0
-
Trait: Vitamin B12
- Mapped Trait(s):
- Samples: 51,453
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 164,950 (86.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003162
Reference score
- Variants: 10,318,272
- Variants ignored: 0
-
Trait: Vitamin B12
- Mapped Trait(s):
- Samples: 51,453
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 9,801,276 (94.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003163
Reference score
- Variants: 1,113,819
- Variants ignored: 0
-
Trait: Vitamin B12
- Mapped Trait(s):
- Samples: 51,453
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,819 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003164
Reference score
- Variants: 263,612
- Variants ignored: 0
-
Trait: Vitamin B12
- Mapped Trait(s):
- Samples: 1,210
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 260,689 (98.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003165
Reference score
- Variants: 9
- Variants ignored: 0
-
Trait: Vitamin B12
- Mapped Trait(s):
- Samples: 1,210
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 9 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003166
Reference score
- Variants: 9
- Variants ignored: 0
-
Trait: Vitamin B12
- Mapped Trait(s):
- Samples: 1,210
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 9 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003167
Reference score
- Variants: 9,805
- Variants ignored: 0
-
Trait: Vitamin B12
- Mapped Trait(s):
- Samples: 1,210
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 9,767 (99.61%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003168
Reference score
- Variants: 1,100,788
- Variants ignored: 0
-
Trait: Vitamin B12
- Mapped Trait(s):
- Samples: 1,210
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,100,788 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003169
Reference score
- Variants: 291,530
- Variants ignored: 0
-
Trait: Vitamin B12
- Mapped Trait(s):
- Samples: 1,210
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 284,964 (97.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003170
Reference score
- Variants: 2,232
- Variants ignored: 0
-
Trait: Vitamin B12
- Mapped Trait(s):
- Samples: 1,210
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,076 (93.01%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003171
Reference score
- Variants: 2,232
- Variants ignored: 0
-
Trait: Vitamin B12
- Mapped Trait(s):
- Samples: 1,210
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,076 (93.01%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003172
Reference score
- Variants: 5,880
- Variants ignored: 0
-
Trait: Vitamin B12
- Mapped Trait(s):
- Samples: 1,210
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 5,865 (99.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003173
Reference score
- Variants: 1,101,425
- Variants ignored: 0
-
Trait: Vitamin B12
- Mapped Trait(s):
- Samples: 1,210
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,101,425 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003174
Reference score
- Variants: 312,224
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 51,453
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 311,278 (99.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003175
Reference score
- Variants: 11
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 51,453
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 10 (90.91%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003176
Reference score
- Variants: 19
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 51,453
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 18 (94.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003177
Reference score
- Variants: 10,318,270
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 51,453
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 9,801,274 (94.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003178
Reference score
- Variants: 1,113,819
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 51,453
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,819 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003179
Reference score
- Variants: 310,479
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 51,453
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 309,499 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003180
Reference score
- Variants: 5
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 51,453
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 5 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003181
Reference score
- Variants: 15
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 51,453
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 12 (80%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003182
Reference score
- Variants: 10,318,270
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 51,453
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 9,801,274 (94.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003183
Reference score
- Variants: 1,113,819
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 51,453
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,819 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003184
Reference score
- Variants: 108,547
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 79,366
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 108,215 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003185
Reference score
- Variants: 16
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 79,366
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 16 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003186
Reference score
- Variants: 15
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 79,366
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 15 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003187
Reference score
- Variants: 98,135
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 79,366
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 97,948 (99.81%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003188
Reference score
- Variants: 1,058,027
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 79,366
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,058,027 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003189
Reference score
- Variants: 547,654
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 329,247
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 545,976 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003190
Reference score
- Variants: 495
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 329,247
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 492 (99.39%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003191
Reference score
- Variants: 605
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 329,247
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 577 (95.37%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003192
Reference score
- Variants: 10,313,259
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 329,247
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 9,783,687 (94.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003193
Reference score
- Variants: 1,113,831
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 329,247
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,831 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003194
Reference score
- Variants: 548,161
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 329,247
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 546,475 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003195
Reference score
- Variants: 404
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 329,247
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 401 (99.26%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003196
Reference score
- Variants: 500
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 329,247
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 475 (95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003197
Reference score
- Variants: 10,313,258
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 329,247
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 9,783,686 (94.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003198
Reference score
- Variants: 1,113,831
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 329,247
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,831 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003199
Reference score
- Variants: 109,290
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 79,366
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 108,932 (99.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003200
Reference score
- Variants: 23
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 79,366
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 23 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003201
Reference score
- Variants: 22
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 79,366
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 22 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003202
Reference score
- Variants: 805,427
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 79,366
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 802,746 (99.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003203
Reference score
- Variants: 1,058,756
- Variants ignored: 0
-
Trait: Vitamin D
- Mapped Trait(s):
- Samples: 79,366
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,058,756 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003204
Reference score
- Variants: 4,360
- Variants ignored: 0
-
Trait: Sleep Apnea
- Mapped Trait(s):
- Samples: 176,232
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 4,026 (92.34%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003205
Reference score
- Variants: 5,300
- Variants ignored: 0
-
Trait: Sleep Apnea
- Mapped Trait(s):
- Samples: 176,232
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 4,097 (77.3%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003206
Reference score
- Variants: 9,873
- Variants ignored: 0
-
Trait: Sleep Apnea
- Mapped Trait(s):
- Samples: 176,232
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,456 (75.52%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003207
Reference score
- Variants: 355
- Variants ignored: 0
-
Trait: Sleep Apnea
- Mapped Trait(s):
- Samples: 176,232
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 291 (81.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003208
Reference score
- Variants: 12,076
- Variants ignored: 0
-
Trait: Sleep Apnea
- Mapped Trait(s):
- Samples: 176,232
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 12,076 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003209
Reference score
- Variants: 328,671
- Variants ignored: 0
-
Trait: Sleep Apnea
- Mapped Trait(s):
- Samples: 358,945
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 327,609 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003210
Reference score
- Variants: 40,992
- Variants ignored: 0
-
Trait: Sleep Apnea
- Mapped Trait(s):
- Samples: 358,945
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 39,049 (95.26%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003211
Reference score
- Variants: 39,223
- Variants ignored: 0
-
Trait: Sleep Apnea
- Mapped Trait(s):
- Samples: 358,945
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 39,054 (99.57%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003212
Reference score
- Variants: 7,601,206
- Variants ignored: 0
-
Trait: Sleep Apnea
- Mapped Trait(s):
- Samples: 358,945
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,577,000 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003213
Reference score
- Variants: 1,111,194
- Variants ignored: 0
-
Trait: Sleep Apnea
- Mapped Trait(s):
- Samples: 358,945
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,111,194 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003214
Reference score
- Variants: 5,812
- Variants ignored: 0
-
Trait: Sleep Apnea
- Mapped Trait(s):
- Samples: 176,232
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 5,027 (86.49%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003215
Reference score
- Variants: 1,209
- Variants ignored: 0
-
Trait: Sleep Apnea
- Mapped Trait(s):
- Samples: 176,232
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 793 (65.59%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003216
Reference score
- Variants: 688
- Variants ignored: 0
-
Trait: Sleep Apnea
- Mapped Trait(s):
- Samples: 176,232
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 483 (70.2%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003217
Reference score
- Variants: 46
- Variants ignored: 0
-
Trait: Sleep Apnea
- Mapped Trait(s):
- Samples: 176,232
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 29 (63.04%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003218
Reference score
- Variants: 12,097
- Variants ignored: 0
-
Trait: Sleep Apnea
- Mapped Trait(s):
- Samples: 176,232
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 12,097 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003219
Reference score
- Variants: 443,281
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate
- Mapped Trait(s):
- Samples: 783,978
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 442,099 (99.73%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003220
Reference score
- Variants: 2,439
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate
- Mapped Trait(s):
- Samples: 783,978
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,430 (99.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003221
Reference score
- Variants: 2,491
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate
- Mapped Trait(s):
- Samples: 783,978
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,482 (99.64%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003222
Reference score
- Variants: 4,656,243
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate
- Mapped Trait(s):
- Samples: 783,978
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 4,642,710 (99.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003223
Reference score
- Variants: 1,117,334
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate
- Mapped Trait(s):
- Samples: 783,978
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,117,334 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003224
Reference score
- Variants: 456,946
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate
- Mapped Trait(s):
- Samples: 783,978
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 455,764 (99.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003225
Reference score
- Variants: 2,092
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate
- Mapped Trait(s):
- Samples: 783,978
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,086 (99.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003226
Reference score
- Variants: 2,127
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate
- Mapped Trait(s):
- Samples: 783,978
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,121 (99.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003227
Reference score
- Variants: 4,728,961
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate
- Mapped Trait(s):
- Samples: 783,978
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 4,715,594 (99.72%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003228
Reference score
- Variants: 1,118,118
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate
- Mapped Trait(s):
- Samples: 783,978
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,118,118 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003229
Reference score
- Variants: 557,260
- Variants ignored: 0
-
Trait: Creatine
- Mapped Trait(s):
- Samples: 350,812
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 555,412 (99.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003230
Reference score
- Variants: 11,173
- Variants ignored: 0
-
Trait: Creatine
- Mapped Trait(s):
- Samples: 350,812
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 10,860 (97.2%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003231
Reference score
- Variants: 19,491
- Variants ignored: 0
-
Trait: Creatine
- Mapped Trait(s):
- Samples: 350,812
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 17,613 (90.36%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003232
Reference score
- Variants: 7,062,258
- Variants ignored: 0
-
Trait: Creatine
- Mapped Trait(s):
- Samples: 350,812
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 6,649,358 (94.15%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003233
Reference score
- Variants: 1,113,832
- Variants ignored: 0
-
Trait: Creatine
- Mapped Trait(s):
- Samples: 350,812
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,832 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003234
Reference score
- Variants: 530,378
- Variants ignored: 0
-
Trait: Creatine
- Mapped Trait(s):
- Samples: 350,812
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 528,640 (99.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003235
Reference score
- Variants: 10,760
- Variants ignored: 0
-
Trait: Creatine
- Mapped Trait(s):
- Samples: 350,812
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 10,380 (96.47%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003236
Reference score
- Variants: 19,006
- Variants ignored: 0
-
Trait: Creatine
- Mapped Trait(s):
- Samples: 350,812
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 17,099 (89.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003237
Reference score
- Variants: 7,021,804
- Variants ignored: 0
-
Trait: Creatine
- Mapped Trait(s):
- Samples: 350,812
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 6,609,931 (94.13%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003238
Reference score
- Variants: 1,113,832
- Variants ignored: 0
-
Trait: Creatine
- Mapped Trait(s):
- Samples: 350,812
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,832 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003239
Reference score
- Variants: 828,634
- Variants ignored: 0
-
Trait: Creatine
- Mapped Trait(s):
- Samples: 344,104
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 826,072 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003240
Reference score
- Variants: 19,120
- Variants ignored: 0
-
Trait: Creatine
- Mapped Trait(s):
- Samples: 344,104
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 18,525 (96.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003241
Reference score
- Variants: 29,361
- Variants ignored: 0
-
Trait: Creatine
- Mapped Trait(s):
- Samples: 344,104
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 26,990 (91.92%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003242
Reference score
- Variants: 7,451,744
- Variants ignored: 0
-
Trait: Creatine
- Mapped Trait(s):
- Samples: 344,104
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,015,366 (94.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003243
Reference score
- Variants: 1,113,831
- Variants ignored: 0
-
Trait: Creatine
- Mapped Trait(s):
- Samples: 344,104
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,831 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003244
Reference score
- Variants: 638,561
- Variants ignored: 0
-
Trait: Creatine
- Mapped Trait(s):
- Samples: 344,104
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 636,580 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003245
Reference score
- Variants: 3,503
- Variants ignored: 0
-
Trait: Creatine
- Mapped Trait(s):
- Samples: 344,104
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 3,348 (95.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003246
Reference score
- Variants: 6,012
- Variants ignored: 0
-
Trait: Creatine
- Mapped Trait(s):
- Samples: 344,104
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 5,232 (87.03%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003247
Reference score
- Variants: 7,451,626
- Variants ignored: 0
-
Trait: Creatine
- Mapped Trait(s):
- Samples: 344,104
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,015,234 (94.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003248
Reference score
- Variants: 1,113,831
- Variants ignored: 0
-
Trait: Creatine
- Mapped Trait(s):
- Samples: 344,104
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,831 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003249
Reference score
- Variants: 202,159
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 24,061
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 201,563 (99.71%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003250
Reference score
- Variants: 108
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 24,061
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 107 (99.07%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003251
Reference score
- Variants: 108
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 24,061
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 107 (99.07%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003252
Reference score
- Variants: 59,729
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 24,061
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 59,428 (99.5%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003253
Reference score
- Variants: 1,109,085
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 24,061
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,109,085 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003254
Reference score
- Variants: 2,986
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 111,666
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,986 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003255
Reference score
- Variants: 352
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 111,666
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 352 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003256
Reference score
- Variants: 641
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 111,666
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 533 (83.15%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003257
Reference score
- Variants: 3,145
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 111,666
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,975 (94.59%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003258
Reference score
- Variants: 16,682
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 111,666
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 16,682 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003259
Reference score
- Variants: 87,064
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 133,814
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 86,798 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003260
Reference score
- Variants: 234
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 133,814
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 234 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003261
Reference score
- Variants: 234
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 133,814
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 234 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003262
Reference score
- Variants: 1,005,540
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 133,814
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,001,748 (99.62%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003263
Reference score
- Variants: 932,548
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 133,814
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 932,548 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003264
Reference score
- Variants: 214,280
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 24,061
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 213,389 (99.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003265
Reference score
- Variants: 176
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 24,061
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 175 (99.43%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003266
Reference score
- Variants: 176
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 24,061
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 175 (99.43%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003267
Reference score
- Variants: 22,376
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 24,061
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 22,232 (99.36%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003268
Reference score
- Variants: 1,109,812
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 24,061
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,109,812 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003269
Reference score
- Variants: 2,989
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 111,666
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,989 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003270
Reference score
- Variants: 314
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 111,666
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 314 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003271
Reference score
- Variants: 600
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 111,666
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 494 (82.33%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003272
Reference score
- Variants: 2,305
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 111,666
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2,180 (94.58%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003273
Reference score
- Variants: 16,686
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 111,666
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 16,686 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003274
Reference score
- Variants: 87,693
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 133,814
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 87,412 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003275
Reference score
- Variants: 458
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 133,814
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 456 (99.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003276
Reference score
- Variants: 458
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 133,814
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 456 (99.56%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003277
Reference score
- Variants: 963,494
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 133,814
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 959,691 (99.61%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003278
Reference score
- Variants: 932,878
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Creatine)
- Mapped Trait(s):
- Samples: 133,814
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 932,878 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003279
Reference score
- Variants: 879,560
- Variants ignored: 0
-
Trait: Cystatin C
- Mapped Trait(s):
- Samples: 344,264
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 876,788 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003280
Reference score
- Variants: 346
- Variants ignored: 0
-
Trait: Cystatin C
- Mapped Trait(s):
- Samples: 344,264
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 340 (98.27%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003281
Reference score
- Variants: 415
- Variants ignored: 0
-
Trait: Cystatin C
- Mapped Trait(s):
- Samples: 344,264
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 402 (96.87%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003282
Reference score
- Variants: 7,451,904
- Variants ignored: 0
-
Trait: Cystatin C
- Mapped Trait(s):
- Samples: 344,264
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,015,488 (94.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003283
Reference score
- Variants: 1,113,831
- Variants ignored: 0
-
Trait: Cystatin C
- Mapped Trait(s):
- Samples: 344,264
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,831 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003284
Reference score
- Variants: 735,756
- Variants ignored: 0
-
Trait: Cystatin C
- Mapped Trait(s):
- Samples: 344,264
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 733,414 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003285
Reference score
- Variants: 931
- Variants ignored: 0
-
Trait: Cystatin C
- Mapped Trait(s):
- Samples: 344,264
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 907 (97.42%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003286
Reference score
- Variants: 1,057
- Variants ignored: 0
-
Trait: Cystatin C
- Mapped Trait(s):
- Samples: 344,264
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,025 (96.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003287
Reference score
- Variants: 7,451,726
- Variants ignored: 0
-
Trait: Cystatin C
- Mapped Trait(s):
- Samples: 344,264
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7,015,318 (94.14%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003288
Reference score
- Variants: 1,113,831
- Variants ignored: 0
-
Trait: Cystatin C
- Mapped Trait(s):
- Samples: 344,264
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,831 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003289
Reference score
- Variants: 162,595
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 110,527
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 162,040 (99.66%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003290
Reference score
- Variants: 48
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 110,527
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 48 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003291
Reference score
- Variants: 49
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 110,527
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 49 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003292
Reference score
- Variants: 88,980
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 110,527
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 88,694 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003293
Reference score
- Variants: 1,114,109
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 110,527
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,114,109 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003294
Reference score
- Variants: 1,954
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 32,861
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,954 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003295
Reference score
- Variants: 42
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 32,861
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 42 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003296
Reference score
- Variants: 87
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 32,861
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 67 (77.01%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003297
Reference score
- Variants: 7,372
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 32,861
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 6,905 (93.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003298
Reference score
- Variants: 16,681
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 32,861
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 16,681 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003299
Reference score
- Variants: 62,133
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 33,152
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 61,940 (99.69%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003300
Reference score
- Variants: 203
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 33,152
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 203 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003301
Reference score
- Variants: 204
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 33,152
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 204 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003302
Reference score
- Variants: 695,827
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 33,152
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 694,566 (99.82%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003303
Reference score
- Variants: 933,013
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 33,152
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 933,013 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003304
Reference score
- Variants: 174,315
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 110,527
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 173,481 (99.52%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003305
Reference score
- Variants: 15
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 110,527
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 15 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003306
Reference score
- Variants: 15
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 110,527
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 15 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003307
Reference score
- Variants: 11,672
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 110,527
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 11,606 (99.43%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003308
Reference score
- Variants: 1,114,999
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 110,527
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,114,999 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003309
Reference score
- Variants: 1,954
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 32,861
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,954 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003310
Reference score
- Variants: 6
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 32,861
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 6 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003311
Reference score
- Variants: 7
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 32,861
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 7 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003312
Reference score
- Variants: 6,375
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 32,861
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 5,979 (93.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003313
Reference score
- Variants: 16,685
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 32,861
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 16,685 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003314
Reference score
- Variants: 62,626
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 33,152
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 62,419 (99.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003315
Reference score
- Variants: 2
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 33,152
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003316
Reference score
- Variants: 2
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 33,152
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 2 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003317
Reference score
- Variants: 594,334
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 33,152
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 593,157 (99.8%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003318
Reference score
- Variants: 933,341
- Variants ignored: 0
-
Trait: estimated glomerular filtration rate (Cystatin C)
- Mapped Trait(s):
- Samples: 33,152
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 933,341 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003319
Reference score
- Variants: 578,551
- Variants ignored: 0
-
Trait: Insomnia
- Mapped Trait(s):
- Samples: 359,020
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 576,705 (99.68%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003320
Reference score
- Variants: 147
- Variants ignored: 0
-
Trait: Insomnia
- Mapped Trait(s):
- Samples: 359,020
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 146 (99.32%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003321
Reference score
- Variants: 148
- Variants ignored: 0
-
Trait: Insomnia
- Mapped Trait(s):
- Samples: 359,020
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 146 (98.65%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003322
Reference score
- Variants: 8,590,163
- Variants ignored: 0
-
Trait: Insomnia
- Mapped Trait(s):
- Samples: 359,020
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 8,150,329 (94.88%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003323
Reference score
- Variants: 1,113,832
- Variants ignored: 0
-
Trait: Insomnia
- Mapped Trait(s):
- Samples: 359,020
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,113,832 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003324
Reference score
- Variants: 464,576
- Variants ignored: 0
-
Trait: Insomnia
- Mapped Trait(s):
- Samples: 360,738
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 463,176 (99.7%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003325
Reference score
- Variants: 28,289
- Variants ignored: 0
-
Trait: Insomnia
- Mapped Trait(s):
- Samples: 360,738
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 27,336 (96.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003326
Reference score
- Variants: 27,462
- Variants ignored: 0
-
Trait: Insomnia
- Mapped Trait(s):
- Samples: 360,738
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 27,339 (99.55%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003327
Reference score
- Variants: 6,214,923
- Variants ignored: 0
-
Trait: Insomnia
- Mapped Trait(s):
- Samples: 360,738
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 6,194,661 (99.67%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003328
Reference score
- Variants: 1,065,129
- Variants ignored: 0
-
Trait: Insomnia
- Mapped Trait(s):
- Samples: 360,738
- Population:
- Publication: Ma Y et.al, Am J Hum Genet (2022-09-23)
- View in PGS-Catalog
Target study
- Coverage: 1,065,129 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003329
Reference score
- Variants: 19
- Variants ignored: 0
-
Trait: Gout
- Mapped Trait(s):
- Samples: 332,370
- Population:
- Publication: Sumpter NA et.al, Arthritis Rheumatol (2022-10-25)
- View in PGS-Catalog
Target study
- Coverage: 18 (94.74%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003330
Reference score
- Variants: 10
- Variants ignored: 0
-
Trait: Factor VIII levels
- Mapped Trait(s):
- Samples: 32,610
- Population:
- European: 79.4%
- African: 13.8%
- Hispanic or Latin American: 4.4%
- Multi-Ancestry (excluding Europeans): 2.4%
- Publication: Valenti L et.al, JHEP Rep (2022-09-25)
- View in PGS-Catalog
Target study
- Coverage: 0 (0%) zero
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003331
Reference score
- Variants: 290
- Variants ignored: 0
-
Trait: Prostate cancer
- Mapped Trait(s):
- Samples: 234,253
- Population:
- European: 75.8%
- East Asian: 11.7%
- Multi-Ancestry (excluding Europeans): 9.1%
- Hispanic or Latin American: 3.4%
- Publication: Huynh-Le MP et.al, Prostate Cancer Prostatic Dis (2022-02-12)
- View in PGS-Catalog
Target study
- Coverage: 272 (93.79%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003333
Reference score
- Variants: 1,088,415
- Variants ignored: 0
-
Trait: Major Depressive Disorder
- Mapped Trait(s):
- Samples: 807,553
- Population:
- Publication: Fang Y et.al, Biol Psychiatry (2022-06-11)
- View in PGS-Catalog
Target study
- Coverage: 1,088,415 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003334
Reference score
- Variants: 27
- Variants ignored: 0
-
Trait: Dementia
- Mapped Trait(s):
- Samples: 63,926
- Population:
- Publication: Chen Y et.al, Arch Gerontol Geriatr (2022-10-31)
- View in PGS-Catalog
Target study
- Coverage: 13 (48.15%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003335
Reference score
- Variants: 18
- Variants ignored: 0
-
Trait: Bladder cancer
- Mapped Trait(s):
- Samples: 36,139
- Population:
- Publication: Teleka S et.al, Sci Rep (2022-10-31)
- View in PGS-Catalog
Target study
- Coverage: 16 (88.89%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003336
Reference score
- Variants: 56
- Variants ignored: 11
-
Trait: Fasting plasma glucose
- Mapped Trait(s):
- Samples: 288,127
- Population:
- Publication: Kim YJ et.al, Nat Commun (2022-11-04)
- View in PGS-Catalog
Target study
- Coverage: 39 (69.64%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003337
Reference score
- Variants: 68
- Variants ignored: 13
-
Trait: Hemoglobin A1c level
- Mapped Trait(s):
- Samples: 288,127
- Population:
- Publication: Kim YJ et.al, Nat Commun (2022-11-04)
- View in PGS-Catalog
Target study
- Coverage: 50 (73.53%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003338
Reference score
- Variants: 79
- Variants ignored: 16
-
Trait: HDL cholesterol level
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 288,127
- Population:
- Publication: Kim YJ et.al, Nat Commun (2022-11-04)
- View in PGS-Catalog
Target study
- Coverage: 61 (77.22%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003339
Reference score
- Variants: 65
- Variants ignored: 10
-
Trait: LDL cholesterol level
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 288,127
- Population:
- Publication: Kim YJ et.al, Nat Commun (2022-11-04)
- View in PGS-Catalog
Target study
- Coverage: 53 (81.54%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003340
Reference score
- Variants: 65
- Variants ignored: 11
-
Trait: Triglyceride level
- Mapped Trait(s):
- Samples: 288,127
- Population:
- Publication: Kim YJ et.al, Nat Commun (2022-11-04)
- View in PGS-Catalog
Target study
- Coverage: 52 (80%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003341
Reference score
- Variants: 91
- Variants ignored: 23
-
Trait: Total cholesterol
- Mapped Trait(s):
- Samples: 288,127
- Population:
- Publication: Kim YJ et.al, Nat Commun (2022-11-04)
- View in PGS-Catalog
Target study
- Coverage: 63 (69.23%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003342
Reference score
- Variants: 51
- Variants ignored: 14
-
Trait: Alanine aminotransferase level
- Mapped Trait(s):
- EFO_0004735: serum alanine aminotransferase measurement
- Samples: 288,127
- Population:
- Publication: Kim YJ et.al, Nat Commun (2022-11-04)
- View in PGS-Catalog
Target study
- Coverage: 37 (72.55%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003343
Reference score
- Variants: 54
- Variants ignored: 11
-
Trait: Aspartate aminotransferase level
- Mapped Trait(s):
- Samples: 288,127
- Population:
- Publication: Kim YJ et.al, Nat Commun (2022-11-04)
- View in PGS-Catalog
Target study
- Coverage: 43 (79.63%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003344
Reference score
- Variants: 82
- Variants ignored: 21
-
Trait: Gamma glutamyl transferase level
- Mapped Trait(s):
- EFO_0004532: serum gamma-glutamyl transferase measurement
- Samples: 288,127
- Population:
- Publication: Kim YJ et.al, Nat Commun (2022-11-04)
- View in PGS-Catalog
Target study
- Coverage: 59 (71.95%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003345
Reference score
- Variants: 60
- Variants ignored: 11
-
Trait: Fasting plasma glucose
- Mapped Trait(s):
- Samples: 288,127
- Population:
- Publication: Kim YJ et.al, Nat Commun (2022-11-04)
- View in PGS-Catalog
Target study
- Coverage: 41 (68.33%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003346
Reference score
- Variants: 74
- Variants ignored: 14
-
Trait: Hemoglobin A1c level
- Mapped Trait(s):
- Samples: 288,127
- Population:
- Publication: Kim YJ et.al, Nat Commun (2022-11-04)
- View in PGS-Catalog
Target study
- Coverage: 52 (70.27%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003347
Reference score
- Variants: 92
- Variants ignored: 18
-
Trait: HDL cholesterol level
- Mapped Trait(s):
- EFO_0004612: high density lipoprotein cholesterol measurement
- Samples: 288,127
- Population:
- Publication: Kim YJ et.al, Nat Commun (2022-11-04)
- View in PGS-Catalog
Target study
- Coverage: 68 (73.91%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003348
Reference score
- Variants: 78
- Variants ignored: 11
-
Trait: LDL cholesterol level
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 288,127
- Population:
- Publication: Kim YJ et.al, Nat Commun (2022-11-04)
- View in PGS-Catalog
Target study
- Coverage: 59 (75.64%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003349
Reference score
- Variants: 76
- Variants ignored: 13
-
Trait: Triglyceride level
- Mapped Trait(s):
- Samples: 288,127
- Population:
- Publication: Kim YJ et.al, Nat Commun (2022-11-04)
- View in PGS-Catalog
Target study
- Coverage: 53 (69.74%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003350
Reference score
- Variants: 102
- Variants ignored: 23
-
Trait: Total cholesterol
- Mapped Trait(s):
- Samples: 288,127
- Population:
- Publication: Kim YJ et.al, Nat Commun (2022-11-04)
- View in PGS-Catalog
Target study
- Coverage: 69 (67.65%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003352
Reference score
- Variants: 56
- Variants ignored: 12
-
Trait: Aspartate aminotransferase level
- Mapped Trait(s):
- Samples: 288,127
- Population:
- Publication: Kim YJ et.al, Nat Commun (2022-11-04)
- View in PGS-Catalog
Target study
- Coverage: 44 (78.57%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003353
Reference score
- Variants: 287
- Variants ignored: 0
-
Trait: Type 2 diabetes
- Mapped Trait(s):
- Samples: 433,540
- Population:
- Publication: Kim YJ et.al, Nat Commun (2022-11-04)
- View in PGS-Catalog
Target study
- Coverage: 287 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003354
Reference score
- Variants: 5
- Variants ignored: 1
-
Trait: Childhood steroid-sensitive nephrotic syndrome
- Mapped Trait(s):
- Samples: 6,064
- Population:
- Publication: Downie ML et.al, Pediatr Nephrol (2022-11-10)
- View in PGS-Catalog
Target study
- Coverage: 4 (80%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003355
Reference score
- Variants: 1,532,758
- Variants ignored: 0
-
Trait: Coronary artery disease
- Mapped Trait(s):
- Samples: 187,599
- Population:
- European: 75.3%
- South Asian: 13.6%
- East Asian: 6%
- Hispanic or Latin American: 2.2%
- African: 1.7%
- Greater Middle Eastern: 1.2%
- Publication: Aragam KG et.al, Nat Genet (2022-12-06)
- View in PGS-Catalog
Target study
- Coverage: 1,532,004 (99.95%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003356
Reference score
- Variants: 2,324,683
- Variants ignored: 0
-
Trait: Coronary artery disease
- Mapped Trait(s):
- Samples: 1,165,690
- Population:
- Multi-Ancestry (including Europeans): 100%
- Publication: Aragam KG et.al, Nat Genet (2022-12-06)
- View in PGS-Catalog
Target study
- Coverage: 2,323,974 (99.97%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003357
Reference score
- Variants: 1,194,472
- Variants ignored: 0
-
Trait: Smoking initiation
- Mapped Trait(s):
- Samples: 24,278
- Population:
- Publication: Saunders GRB et.al, Nature (2022-12-07)
- View in PGS-Catalog
Target study
- Coverage: 16,837 (1.41%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003358
Reference score
- Variants: 1,109,850
- Variants ignored: 0
-
Trait: Smoking initiation
- Mapped Trait(s):
- Samples: 7,019
- Population:
- Hispanic or Latin American: 100%
- Publication: Saunders GRB et.al, Nature (2022-12-07)
- View in PGS-Catalog
Target study
- Coverage: 15,786 (1.42%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003359
Reference score
- Variants: 859,206
- Variants ignored: 0
-
Trait: Smoking initiation
- Mapped Trait(s):
- Samples: 217,901
- Population:
- Publication: Saunders GRB et.al, Nature (2022-12-07)
- View in PGS-Catalog
Target study
- Coverage: 12,310 (1.43%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003360
Reference score
- Variants: 1,055,915
- Variants ignored: 0
-
Trait: Smoking initiation
- Mapped Trait(s):
- Samples: 805,431
- Population:
- Publication: Saunders GRB et.al, Nature (2022-12-07)
- View in PGS-Catalog
Target study
- Coverage: 15,073 (1.43%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003361
Reference score
- Variants: 1,193,754
- Variants ignored: 0
-
Trait: Age of smoking initiation
- Mapped Trait(s):
- Samples: 10,447
- Population:
- Publication: Saunders GRB et.al, Nature (2022-12-07)
- View in PGS-Catalog
Target study
- Coverage: 16,829 (1.41%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003362
Reference score
- Variants: 1,073,689
- Variants ignored: 0
-
Trait: Age of smoking initiation
- Mapped Trait(s):
- Samples: 844
- Population:
- Hispanic or Latin American: 100%
- Publication: Saunders GRB et.al, Nature (2022-12-07)
- View in PGS-Catalog
Target study
- Coverage: 15,287 (1.42%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003363
Reference score
- Variants: 858,406
- Variants ignored: 0
-
Trait: Age of smoking initiation
- Mapped Trait(s):
- Samples: 59,148
- Population:
- Publication: Saunders GRB et.al, Nature (2022-12-07)
- View in PGS-Catalog
Target study
- Coverage: 12,308 (1.43%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003364
Reference score
- Variants: 1,055,960
- Variants ignored: 0
-
Trait: Age of smoking initiation
- Mapped Trait(s):
- Samples: 323,386
- Population:
- Publication: Saunders GRB et.al, Nature (2022-12-07)
- View in PGS-Catalog
Target study
- Coverage: 15,069 (1.43%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003365
Reference score
- Variants: 1,196,168
- Variants ignored: 0
-
Trait: Cigarettes smoked per day
- Mapped Trait(s):
- Samples: 13,307
- Population:
- Publication: Saunders GRB et.al, Nature (2022-12-07)
- View in PGS-Catalog
Target study
- Coverage: 16,882 (1.41%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003366
Reference score
- Variants: 1,112,206
- Variants ignored: 0
-
Trait: Cigarettes smoked per day
- Mapped Trait(s):
- Samples: 5,276
- Population:
- Hispanic or Latin American: 100%
- Publication: Saunders GRB et.al, Nature (2022-12-07)
- View in PGS-Catalog
Target study
- Coverage: 15,832 (1.42%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003367
Reference score
- Variants: 858,414
- Variants ignored: 0
-
Trait: Cigarettes smoked per day
- Mapped Trait(s):
- Samples: 104,665
- Population:
- Publication: Saunders GRB et.al, Nature (2022-12-07)
- View in PGS-Catalog
Target study
- Coverage: 12,308 (1.43%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003368
Reference score
- Variants: 1,055,811
- Variants ignored: 0
-
Trait: Cigarettes smoked per day
- Mapped Trait(s):
- Samples: 326,497
- Population:
- Publication: Saunders GRB et.al, Nature (2022-12-07)
- View in PGS-Catalog
Target study
- Coverage: 15,066 (1.43%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003369
Reference score
- Variants: 1,193,789
- Variants ignored: 0
-
Trait: Smoking cessation
- Mapped Trait(s):
- Samples: 11,438
- Population:
- Publication: Saunders GRB et.al, Nature (2022-12-07)
- View in PGS-Catalog
Target study
- Coverage: 16,830 (1.41%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003370
Reference score
- Variants: 1,109,663
- Variants ignored: 0
-
Trait: Smoking cessation
- Mapped Trait(s):
- Samples: 2,447
- Population:
- Hispanic or Latin American: 100%
- Publication: Saunders GRB et.al, Nature (2022-12-07)
- View in PGS-Catalog
Target study
- Coverage: 15,784 (1.42%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003371
Reference score
- Variants: 859,229
- Variants ignored: 0
-
Trait: Smoking cessation
- Mapped Trait(s):
- Samples: 106,993
- Population:
- Publication: Saunders GRB et.al, Nature (2022-12-07)
- View in PGS-Catalog
Target study
- Coverage: 12,311 (1.43%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003372
Reference score
- Variants: 1,055,802
- Variants ignored: 0
-
Trait: Smoking cessation
- Mapped Trait(s):
- Samples: 388,313
- Population:
- Publication: Saunders GRB et.al, Nature (2022-12-07)
- View in PGS-Catalog
Target study
- Coverage: 15,069 (1.43%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003373
Reference score
- Variants: 1,177,071
- Variants ignored: 0
-
Trait: Drinks per week
- Mapped Trait(s):
- Samples: 8,078
- Population:
- Publication: Saunders GRB et.al, Nature (2022-12-07)
- View in PGS-Catalog
Target study
- Coverage: 16,649 (1.41%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003374
Reference score
- Variants: 1,109,568
- Variants ignored: 0
-
Trait: Drinks per week
- Mapped Trait(s):
- Samples: 5,162
- Population:
- Hispanic or Latin American: 100%
- Publication: Saunders GRB et.al, Nature (2022-12-07)
- View in PGS-Catalog
Target study
- Coverage: 15,800 (1.42%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003375
Reference score
- Variants: 856,333
- Variants ignored: 0
-
Trait: Drinks per week
- Mapped Trait(s):
- Samples: 90,852
- Population:
- Publication: Saunders GRB et.al, Nature (2022-12-07)
- View in PGS-Catalog
Target study
- Coverage: 12,288 (1.43%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003376
Reference score
- Variants: 1,055,988
- Variants ignored: 0
-
Trait: Drinks per week
- Mapped Trait(s):
- Samples: 666,978
- Population:
- Publication: Saunders GRB et.al, Nature (2022-12-07)
- View in PGS-Catalog
Target study
- Coverage: 15,070 (1.43%) low
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003377
Reference score
- Variants: 1,496,254
- Variants ignored: 0
-
Trait: Estimated glomerular filtration rate
- Mapped Trait(s):
- Samples: 406,350
- Population:
- Publication: Steinbrenner I et.al, Kidney Int (2022-12-05)
- View in PGS-Catalog
Target study
- Coverage: 1,496,254 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003380
Reference score
- Variants: 1,142,637
- Variants ignored: 0
-
Trait: Breast cancer
- Mapped Trait(s):
- Samples: 247,173
- Population:
- Publication: Namba S et.al, Cancer Res (2022-10-26)
- View in PGS-Catalog
Target study
- Coverage: 1,141,965 (99.94%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003381
Reference score
- Variants: 529,365
- Variants ignored: 0
-
Trait: Uterine endometrial carcinoma
- Mapped Trait(s):
- Samples: 121,885
- Population:
- Publication: Namba S et.al, Cancer Res (2022-10-26)
- View in PGS-Catalog
Target study
- Coverage: 529,365 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003382
Reference score
- Variants: 672
- Variants ignored: 0
-
Trait: Skin cutaneous melanoma
- Mapped Trait(s):
- Samples: 111,549
- Population:
- Publication: Namba S et.al, Cancer Res (2022-10-26)
- View in PGS-Catalog
Target study
- Coverage: 672 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003383
Reference score
- Variants: 168,700
- Variants ignored: 0
-
Trait: Prostate adenocarcinoma
- Mapped Trait(s):
- Samples: 140,254
- Population:
- Publication: Namba S et.al, Cancer Res (2022-10-26)
- View in PGS-Catalog
Target study
- Coverage: 168,692 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003384
Reference score
- Variants: 910
- Variants ignored: 0
-
Trait: Glioblastoma
- Mapped Trait(s):
- Samples: 15,094
- Population:
- Publication: Namba S et.al, Cancer Res (2022-10-26)
- View in PGS-Catalog
Target study
- Coverage: 910 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003385
Reference score
- Variants: 144,810
- Variants ignored: 0
-
Trait: Ovarian serous carcinoma
- Mapped Trait(s):
- Samples: 54,990
- Population:
- Publication: Namba S et.al, Cancer Res (2022-10-26)
- View in PGS-Catalog
Target study
- Coverage: 144,804 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003386
Reference score
- Variants: 61
- Variants ignored: 0
-
Trait: Colorectal cancer
- Mapped Trait(s):
- Samples: 125,478
- Population:
- European: 95.8%
- East Asian: 4.2%
- Publication: Namba S et.al, Cancer Res (2022-10-26)
- View in PGS-Catalog
Target study
- Coverage: 61 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003387
Reference score
- Variants: 601,980
- Variants ignored: 0
-
Trait: Esophageal adenocarcinoma or Barrett’s esophagus
- Mapped Trait(s):
- Samples: 27,438
- Population:
- Publication: Namba S et.al, Cancer Res (2022-10-26)
- View in PGS-Catalog
Target study
- Coverage: 601,957 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003388
Reference score
- Variants: 356,743
- Variants ignored: 0
-
Trait: Esophageal adenocarcinoma
- Mapped Trait(s):
- Samples: 21,271
- Population:
- Publication: Namba S et.al, Cancer Res (2022-10-26)
- View in PGS-Catalog
Target study
- Coverage: 356,698 (99.99%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003389
Reference score
- Variants: 2,814
- Variants ignored: 0
-
Trait: Cervical cancer
- Mapped Trait(s):
- Samples: 9,347
- Population:
- Publication: Namba S et.al, Cancer Res (2022-10-26)
- View in PGS-Catalog
Target study
- Coverage: 2,814 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003390
Reference score
- Variants: 931,477
- Variants ignored: 0
-
Trait: Head and neck squamous cell carcinoma
- Mapped Trait(s):
- Samples: 12,619
- Population:
- Multi-Ancestry (including Europeans): 90.6%
- Unknown: 9.4%
- Publication: Namba S et.al, Cancer Res (2022-10-26)
- View in PGS-Catalog
Target study
- Coverage: 931,477 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003391
Reference score
- Variants: 133
- Variants ignored: 0
-
Trait: Lung cancer
- Mapped Trait(s):
- Samples: 85,716
- Population:
- Publication: Namba S et.al, Cancer Res (2022-10-26)
- View in PGS-Catalog
Target study
- Coverage: 133 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003392
Reference score
- Variants: 90
- Variants ignored: 0
-
Trait: Lung squamous cell carcinoma
- Mapped Trait(s):
- Samples: 63,053
- Population:
- Publication: Namba S et.al, Cancer Res (2022-10-26)
- View in PGS-Catalog
Target study
- Coverage: 90 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003393
Reference score
- Variants: 74
- Variants ignored: 0
-
Trait: Lung adenocarcinoma
- Mapped Trait(s):
- Samples: 66,756
- Population:
- Publication: Namba S et.al, Cancer Res (2022-10-26)
- View in PGS-Catalog
Target study
- Coverage: 74 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003394
Reference score
- Variants: 36
- Variants ignored: 0
-
Trait: Epithelial ovarian cancer
- Mapped Trait(s):
- Samples: 54,990
- Population:
- Publication: Dareng EO et.al, Eur J Hum Genet (2022-01-14)
- View in PGS-Catalog
Target study
- Coverage: 36 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003396
Reference score
- Variants: 11
- Variants ignored: 0
-
Trait: Breast Cancer
- Mapped Trait(s):
- Samples: 95,283
- Population:
- Publication: Jee YH et.al, Int J Epidemiol (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 11 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003397
Reference score
- Variants: 42
- Variants ignored: 0
-
Trait: Breast Cancer
- Mapped Trait(s):
- Samples: 41,031
- Population:
- Publication: Jee YH et.al, Int J Epidemiol (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 42 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003398
Reference score
- Variants: 136
- Variants ignored: 0
-
Trait: Breast Cancer
- Mapped Trait(s):
- Samples: 139,274
- Population:
- Publication: Jee YH et.al, Int J Epidemiol (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 136 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003399
Reference score
- Variants: 209
- Variants ignored: 0
-
Trait: Breast Cancer
- Mapped Trait(s):
- Samples: 169,092
- Population:
- Publication: Jee YH et.al, Int J Epidemiol (2022-11-07)
- View in PGS-Catalog
Target study
- Coverage: 209 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003400
Reference score
- Variants: 97
- Variants ignored: 18
-
Trait: Obesity
- Mapped Trait(s):
- Samples: 238,944
- Population:
- European: 99.1%
- Hispanic or Latin American: 0.5%
- African: 0.4%
- Publication: Robinson JR et.al, Obesity (Silver Spring) (2022-11-13)
- View in PGS-Catalog
Target study
- Coverage: 78 (80.41%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003401
Reference score
- Variants: 108
- Variants ignored: 0
-
Trait: Triglyceride levels
- Mapped Trait(s):
- Samples: 237,050
- Population:
- Publication: Pieri K et.al, Int J Cardiol (2022-11-19)
- View in PGS-Catalog
Target study
- Coverage: 108 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003402
Reference score
- Variants: 6,838
- Variants ignored: 0
-
Trait: Type 2 Diabetes
- Mapped Trait(s):
- Samples: 110,452
- Population:
- European: 62.5%
- South Asian: 18.1%
- East Asian: 17%
- Hispanic or Latin American: 2.3%
- Publication: Lamri A et.al, Elife (2022-11-22)
- View in PGS-Catalog
Target study
- Coverage: 6,821 (99.75%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003403
Reference score
- Variants: 28
- Variants ignored: 0
-
Trait: LDL cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 94,595
- Population:
- Publication: Trinder M et.al, J Am Coll Cardiol (2019-07-01)
- View in PGS-Catalog
Target study
- Coverage: 0 (0%) zero
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003404
Reference score
- Variants: 10
- Variants ignored: 0
-
Trait: LDL cholesterol
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 19,840
- Population:
- Publication: Wang J et.al, Arterioscler Thromb Vasc Biol (2016-10-20)
- View in PGS-Catalog
Target study
- Coverage: 10 (100%) high
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.
PGS003405
Reference score
- Variants: 169
- Variants ignored: 0
-
Trait: LDL-c blood concentration
- Mapped Trait(s):
- EFO_0004611: low density lipoprotein cholesterol measurement
- Samples: 427,099
- Population:
- Publication: Vanhoye X et.al, Transl Res (2022-12-15)
- View in PGS-Catalog
Target study
- Coverage: 88 (52.07%) medium
- Samples: 51
Distribution
An interactive histogram to investigate samples is available in the extended HTML report.