Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs189014161
rs189014161
KCNH2
0.710 GeneticVariation BEFREE Two of the 13 patients (15%) who presented with QT prolongation and TdP were found to carry long QT syndrome mutations (KCNH2-R744X and SCN5A-E446K). 22338672

2012
dbSNP: rs189014161
rs189014161
KCNH2
A 0.710 CausalMutation CLINVAR