Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs74424227
rs74424227
KCNE2 ; LOC105372791
0.700 GeneticVariation UNIPROT Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test. 19716085

2009
dbSNP: rs74424227
rs74424227
KCNE2 ; LOC105372791
0.700 GeneticVariation UNIPROT Spectrum of pathogenic mutations and associated polymorphisms in a cohort of 44 unrelated patients with long QT syndrome. 16922724

2006
dbSNP: rs74424227
rs74424227
KCNE2 ; LOC105372791
0.700 GeneticVariation UNIPROT Identification and functional characterization of a novel KCNE2 (MiRP1) mutation that alters HERG channel kinetics. 12185453

2002
dbSNP: rs74424227
rs74424227
KCNE2 ; LOC105372791
0.700 GeneticVariation UNIPROT MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia. 10219239

1999