Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199472910
rs199472910
KCNH2
A 0.700 GeneticVariation CLINVAR Contribution of a KCNH2 variant in genotyped long QT syndrome: Romano-Ward syndrome under double mutations and acquired long QT syndrome under heterozygote. 27816319

2017
dbSNP: rs199472910
rs199472910
KCNH2
A 0.700 GeneticVariation CLINVAR Impact of Updated Diagnostic Criteria for Long QT Syndrome on Clinical Detection of Diseased Patients: Results From a Study of Patients Carrying Gene Mutations. 29766885

2016
dbSNP: rs199472910
rs199472910
KCNH2
A 0.700 GeneticVariation CLINVAR Congenital long QT syndrome with compound mutations in the KCNH2 gene. 24057343

2014
dbSNP: rs199472910
rs199472910
KCNH2
A 0.700 GeneticVariation CLINVAR Latent genetic backgrounds and molecular pathogenesis in drug-induced long-QT syndrome. 19843919

2009
dbSNP: rs199472910
rs199472910
KCNH2
A 0.700 GeneticVariation CLINVAR Q-T peak dispersion in congenital long QT syndrome: possible marker of mutation of HERG. 12808265

2003