present in Gene: SCN3B
present in Chromosome: 11
Position on Chromosome: 123642502
Alleles of this Variant: G/A;T
rs587777556 in
SCN3B gene and
Brugada Syndrome 7
PMID 20558140 2010 Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population.
PMID 21051419 2011 Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation.