Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs773724817
rs773724817
KCNH2
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome 		0.710 GeneticVariation BEFREE These data suggest that R863X failed to form functional HERG channels, contributing to a prolongation of the QT interval and long QT syndrome with a dominant phenotype. 14714110

2004