Variant: rs72550247 

    present in Gene: HPN;SCN1B
    present in Chromosome: 19
    Position on Chromosome: 35039125
    Alleles of this Variant: G/A

rs72550247 in HPN;SCN1B gene and ATRIAL FIBRILLATION, FAMILIAL, 13 PMID 19808477 2009 Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation.