rs115099192, GATA4

N. diseases: 5
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.
Tetralogy of Fallot
CUI: C0039685
Disease: Tetralogy of Fallot
83 0.827 0.080 8 11758366 missense variant C/A;G snv 5.1E-04; 6.8E-05 0.810 1.000 1 2010 2010
VENTRICULAR SEPTAL DEFECT 1
CUI: C3280777
Disease: VENTRICULAR SEPTAL DEFECT 1
7 0.827 0.080 8 11758366 missense variant C/A;G snv 5.1E-04; 6.8E-05 0.800 0
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.827 0.080 8 11758366 missense variant C/A;G snv 5.1E-04; 6.8E-05 0.010 1.000 1 2018 2018
Membranous ventricular septum defect
CUI: C0685706
Disease: Membranous ventricular septum defect
2 0.827 0.080 8 11758366 missense variant C/A;G snv 5.1E-04; 6.8E-05 0.010 1.000 1 2010 2010
Perimembranous ventricular septal defect
CUI: C0344925
Disease: Perimembranous ventricular septal defect
3 0.827 0.080 8 11758366 missense variant C/A;G snv 5.1E-04; 6.8E-05 0.010 1.000 1 2010 2010