Variant: rs768049331 

    present in Gene: LOC105377982;TRDN
    present in Chromosome: 6
    Position on Chromosome: 123571099
    Alleles of this Variant: GTCT/-

rs768049331 in LOC105377982;TRDN gene and VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder) PMID 25922419 2015 Homozygous/Compound Heterozygous Triadin Mutations Associated With Autosomal-Recessive Long-QT Syndrome and Pediatric Sudden Cardiac Arrest: Elucidation of the Triadin Knockout Syndrome.

PMID 22422768 2012 Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human.