rs17153694, GATA4

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Alcohol Use Disorder
CUI: C0001956
Disease: Alcohol Use Disorder
54 0.851 0.160 8 11730972 intron variant C/T snv 0.12 0.010 1.000 1 2018 2018
Common ventricle
CUI: C0152424
Disease: Common ventricle
5 0.851 0.160 8 11730972 intron variant C/T snv 0.12 0.010 1.000 1 2019 2019
Single Ventricle Defect
CUI: C3274516
Disease: Single Ventricle Defect
5 0.851 0.160 8 11730972 intron variant C/T snv 0.12 0.010 1.000 1 2019 2019
Tetralogy of Fallot
CUI: C0039685
Disease: Tetralogy of Fallot
83 0.851 0.160 8 11730972 intron variant C/T snv 0.12 0.010 1.000 1 2019 2019