Variant: rs587777558 

    present in Gene: LOC105369543;SCN3B
    present in Chromosome: 11
    Position on Chromosome: 123653785
    Alleles of this Variant: C/T

rs587777558 in LOC105369543;SCN3B gene and Brugada Syndrome 7 PMID 21051419 2011 Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation.

PMID 20558140 2010 Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population.