rs804280, GATA4

N. diseases: 6
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.
Congenital heart disease
CUI: C0152021
Disease: Congenital heart disease
80 0.882 0.120 8 11755189 intron variant C/A;G snv 0.700 1.000 1 2017 2017
Atrial Septal Defects
CUI: C0018817
Disease: Atrial Septal Defects
96 0.882 0.120 8 11755189 intron variant C/A;G snv 0.010 1.000 1 2015 2015
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.882 0.120 8 11755189 intron variant C/A;G snv 0.010 1.000 1 2013 2013
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
123 0.882 0.120 8 11755189 intron variant C/A;G snv 0.010 1.000 1 2013 2013
Tetralogy of Fallot
CUI: C0039685
Disease: Tetralogy of Fallot
83 0.882 0.120 8 11755189 intron variant C/A;G snv 0.010 1.000 1 2015 2015
Ventricular Septal Defects
CUI: C0018818
Disease: Ventricular Septal Defects
87 0.882 0.120 8 11755189 intron variant C/A;G snv 0.010 1.000 1 2015 2015