Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs36210422
rs36210422
KCNH2
0.710 GeneticVariation BEFREE The HERG R176W mutation represents a population-prevalent mutation predisposing to LQTS. 16754261

2006
dbSNP: rs36210422
rs36210422
KCNH2
A 0.710 SusceptibilityMutation CLINVAR