Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12800049
rs12800049
11 16227348 intron variant C/T snv 0.20
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs12801635
rs12801635
11 16330999 intron variant T/C snv 0.17
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs1455114
rs1455114
0.882 0.200 11 16194000 intron variant C/A snv 0.48
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
0.700 1.000 1 2018 2018
dbSNP: rs1455114
rs1455114
0.882 0.200 11 16194000 intron variant C/A snv 0.48
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2018 2018
dbSNP: rs16932777
rs16932777
11 16230637 intron variant C/G snv 0.20
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs2014408
rs2014408
11 16343736 intron variant C/T snv 0.17
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs2014408
rs2014408
11 16343736 intron variant C/T snv 0.17
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2018 2018
dbSNP: rs2218001
rs2218001
11 16320669 intron variant A/C;G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2018 2018
dbSNP: rs2218001
rs2218001
11 16320669 intron variant A/C;G;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
0.700 1.000 1 2018 2018
dbSNP: rs297346
rs297346
1.000 0.040 11 16334225 intron variant A/G;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.700 1.000 1 2018 2018
dbSNP: rs297346
rs297346
1.000 0.040 11 16334225 intron variant A/G;T snv
CUI: C0525045
Disease: Mood Disorders
Mood Disorders
0.700 1.000 1 2018 2018
dbSNP: rs34156428
rs34156428
1.000 0.040 11 16460403 intron variant A/T snv 0.15
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2018 2018
dbSNP: rs35199438
rs35199438
11 16609232 intron variant G/T snv 0.28
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs3809095
rs3809095
11 16736699 intron variant A/G snv 0.21
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs60718933
rs60718933
11 16017007 intron variant T/A;C snv
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2018 2018
dbSNP: rs60718933
rs60718933
11 16017007 intron variant T/A;C snv
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2018 2018
dbSNP: rs7109376
rs7109376
11 16350885 intron variant T/A snv 0.29
CUI: C0018498
Disease: Hair Color
Hair Color
0.700 1.000 1 2018 2018
dbSNP: rs7118275
rs7118275
11 16250132 intron variant C/T snv 0.78
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
0.700 1.000 1 2018 2018
dbSNP: rs7118275
rs7118275
11 16250132 intron variant C/T snv 0.78
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs7131442
rs7131442
11 16326515 intron variant A/T snv 0.17
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs7131442
rs7131442
11 16326515 intron variant A/T snv 0.17
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs7943712
rs7943712
11 16522316 intron variant G/A snv 0.24
CUI: C0018498
Disease: Hair Color
Hair Color
0.700 1.000 1 2018 2018
dbSNP: rs893311
rs893311
11 16296972 intron variant G/T snv 0.16
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs893311
rs893311
11 16296972 intron variant G/T snv 0.16
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
0.700 1.000 1 2018 2018
dbSNP: rs9971406
rs9971406
11 16256743 intron variant G/T snv 0.78
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2018 2018