Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199472765
rs199472765
KCNQ1
0.710 GeneticVariation BEFREE Ion channel mechanisms related to sudden cardiac death in phenotype-negative long-QT syndrome genotype-phenotype correlations of the KCNQ1(S349W) mutation. 20662986

2011
dbSNP: rs199472765
rs199472765
KCNQ1
A 0.710 CausalMutation CLINVAR