Variant: rs199473161 

    present in Gene: SCN5A
    present in Chromosome: 3
    Position on Chromosome: 38586038
    Alleles of this Variant: G/A;T

rs199473161 in SCN5A gene and Brugada Syndrome (disorder) PMID 24815523 2014 Novel SCN5A mutation in amiodarone-responsive multifocal ventricular ectopy-associated cardiomyopathy.

PMID 25179549 2014 Targeted analysis of whole genome sequence data to diagnose genetic cardiomyopathy.

PMID 15671429 2005 Sodium channel mutations and susceptibility to heart failure and atrial fibrillation.

PMID 26733869 2015 Mutations in the Voltage Sensors of Domains I and II of Nav1.5 that are Associated with Arrhythmias and Dilated Cardiomyopathy Generate Gating Pore Currents.

PMID 18048769 2008 Divergent biophysical defects caused by mutant sodium channels in dilated cardiomyopathy with arrhythmia.

rs199473161 in SCN5A gene and Cardiomyopathy, Dilated PMID 24815523 2014 Novel SCN5A mutation in amiodarone-responsive multifocal ventricular ectopy-associated cardiomyopathy.

PMID 18048769 2008 Divergent biophysical defects caused by mutant sodium channels in dilated cardiomyopathy with arrhythmia.

PMID 17442746 2007 Homozygous SCN5A mutation in Brugada syndrome with monomorphic ventricular tachycardia and structural heart abnormalities.

PMID 15671429 2005 Sodium channel mutations and susceptibility to heart failure and atrial fibrillation.