rs121912516, KCNH2

N. diseases: 3
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.
Ventricular Fibrillation
CUI: C0042510
Disease: Ventricular Fibrillation
19 0.882 0.120 7 150951721 missense variant C/G snv 0.010 1.000 1 2008 2008
Ventricular tachycardia, polymorphic
CUI: C0344432
Disease: Ventricular tachycardia, polymorphic
11 0.882 0.120 7 150951721 missense variant C/G snv 0.010 1.000 1 2008 2008
Long Qt Syndrome 2
CUI: C3150943
Disease: Long Qt Syndrome 2
267 0.882 0.120 7 150951721 missense variant C/G snv 0.800 1.000 20 1995 2009