Variant: rs104893713 

    present in Gene: SSUH2;CAV3
    present in Chromosome: 3
    Position on Chromosome: 8745834
    Alleles of this Variant: C/G

rs104893713 in SSUH2;CAV3 gene and LONG QT SYNDROME 9 (disorder) PMID 17275750 2007 Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3.

PMID 17060380 2006 Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome.