Variant: rs11708996 

    present in Gene: SCN5A
    present in Chromosome: 3
    Position on Chromosome: 38592432
    Alleles of this Variant: G/C

rs11708996 in SCN5A gene and Brugada Syndrome (disorder) PMID 23872634 2013 Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.

rs11708996 in SCN5A gene and Electrocardiogram: P-R interval PMID 30046033 2018 PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity.

PMID 31217584 2019 Genetic analyses of diverse populations improves discovery for complex traits.

PMID 20062060 2010 Genome-wide association study of PR interval.

rs11708996 in SCN5A gene and Heart Function Tests PMID 21076409 2010 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.

rs11708996 in SCN5A gene and QRS complex feature PMID 27659466 2016 52 Genetic Loci Influencing Myocardial Mass.

rs11708996 in SCN5A gene and QT interval feature (observable entity) PMID 24952745 2014 Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.