rs794728448, KCNH2

N. diseases: 17
Disease: Congenital long QT syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Congenital long QT syndrome
CUI: C1141890
Disease: Congenital long QT syndrome
0.010 GeneticVariation BEFREE KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome. 16116052 2005