Variant: rs12720441 

    present in Gene: KCNH2
    present in Chromosome: 7
    Position on Chromosome: 150950216
    Alleles of this Variant: G/A;C

rs12720441 in KCNH2 gene and Brugada Syndrome (disorder) PMID 15840476 2005 Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.

PMID 11997281 2002 Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes.

PMID 22949429 2012 Phylogenetic and physicochemical analyses enhance the classification of rare nonsynonymous single nucleotide variants in type 1 and 2 long-QT syndrome.