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 diaphragmatic hernia
CUI: C0235833
Disease: Congenital diaphragmatic hernia
31 0.882 0.120 8 105802189 missense variant A/C;G snv 4.9E-04; 4.0E-06 0.020 1.000 2 2007 2012
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.882 0.120 8 105802189 missense variant A/C;G snv 4.9E-04; 4.0E-06 0.010 1.000 1 2012 2012
Tetralogy of Fallot
CUI: C0039685
Disease: Tetralogy of Fallot
83 0.882 0.120 8 105802189 missense variant A/C;G snv 4.9E-04; 4.0E-06 0.010 1.000 1 2014 2014