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: rs114123510
rs114123510
1.000 0.040 2 202966489 intron variant T/A snv 9.0E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2017 2017
dbSNP: rs138556413
rs138556413
2 202968144 intron variant C/T snv 2.5E-02
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.700 1.000 1 2016 2016
dbSNP: rs140244541
rs140244541
2 202943809 intron variant G/A snv 0.11
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2015 2015
dbSNP: rs149163995
rs149163995
2 202912503 5 prime UTR variant C/T snv 8.7E-02
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.700 1.000 1 2016 2016
dbSNP: rs149268645
rs149268645
0.882 0.040 2 202968295 intron variant G/A snv 8.4E-02
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 1.000 1 2019 2019
dbSNP: rs149268645
rs149268645
0.882 0.040 2 202968295 intron variant G/A snv 8.4E-02
CUI: C0038663
Disease: Suicide attempt
Suicide attempt
0.700 1.000 1 2019 2019
dbSNP: rs149268645
rs149268645
0.882 0.040 2 202968295 intron variant G/A snv 8.4E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 1 2019 2019
dbSNP: rs149268645
rs149268645
0.882 0.040 2 202968295 intron variant G/A snv 8.4E-02
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.700 1.000 1 2019 2019