Variant: rs104894021 

    present in Gene: KCNH2
    present in Chromosome: 7
    Position on Chromosome: 150951629
    Alleles of this Variant: G/C;T

rs104894021 in KCNH2 gene and Short QT Syndrome 1 PMID 14676148 2004 Sudden death associated with short-QT syndrome linked to mutations in HERG.

PMID 15828882 2005 Short QT syndrome and atrial fibrillation caused by mutation in KCNH2.