rs755559514, APLN

N. diseases: 3
Source: BEFREE ×
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.
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
200 0.925 0.040 X 129648648 missense variant T/C;G snv 1.2E-05; 6.1E-06 0.010 1.000 1 2007 2007
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1022 0.925 0.040 X 129648648 missense variant T/C;G snv 1.2E-05; 6.1E-06 0.010 1.000 1 2012 2012
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
871 0.925 0.040 X 129648648 missense variant T/C;G snv 1.2E-05; 6.1E-06 0.010 1 2012 2012