Variant: rs199472910 

    present in Gene: KCNH2
    present in Chromosome: 7
    Position on Chromosome: 150952508
    Alleles of this Variant: G/A

rs199472910 in KCNH2 gene and Congenital long QT syndrome PMID 12808265 2003 Q-T peak dispersion in congenital long QT syndrome: possible marker of mutation of HERG.

PMID 27816319 2017 Contribution of a KCNH2 variant in genotyped long QT syndrome: Romano-Ward syndrome under double mutations and acquired long QT syndrome under heterozygote.

PMID 29766885 2016 Impact of Updated Diagnostic Criteria for Long QT Syndrome on Clinical Detection of Diseased Patients: Results From a Study of Patients Carrying Gene Mutations.

PMID 24057343 2014 Congenital long QT syndrome with compound mutations in the KCNH2 gene.

PMID 19843919 2009 Latent genetic backgrounds and molecular pathogenesis in drug-induced long-QT syndrome.

rs199472910 in KCNH2 gene and Long Qt Syndrome 2 PMID 27041096 2016 Compound Mutations Cause Increased Cardiac Events in Children with Long QT Syndrome: Can the Sequence Homology-Based Tools be Applied for Prediction of Phenotypic Severity?

PMID 27816319 2017 Contribution of a KCNH2 variant in genotyped long QT syndrome: Romano-Ward syndrome under double mutations and acquired long QT syndrome under heterozygote.

PMID 24057343 2014 Congenital long QT syndrome with compound mutations in the KCNH2 gene.

PMID 19843919 2009 Latent genetic backgrounds and molecular pathogenesis in drug-induced long-QT syndrome.