Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912507
rs121912507
KCNH2
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome 		0.710 GeneticVariation BEFREE Isoform-specific dominant-negative effects associated with hERG1 G628S mutation in long QT syndrome. 22876326

2012