Variant: rs6801957 

    present in Gene: SCN10A
    present in Chromosome: 3
    Position on Chromosome: 38725824
    Alleles of this Variant: T/C

rs6801957 in SCN10A gene and Electrocardiogram: P-R interval PMID 21347284 2011 Genome-wide association studies of the PR interval in African Americans.

PMID 30679814 2019 Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits.

PMID 25055868 2014 Genome-wide association study of electrocardiographic parameters identifies a new association for PR interval and confirms previously reported associations.

PMID 23139255 2012 Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts.

PMID 29127183 2018 Genome-wide association study of PR interval in Hispanics/Latinos identifies novel locus at ID2.

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

rs6801957 in SCN10A gene and Heart Function Tests PMID 21076409 2010 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.

rs6801957 in SCN10A gene and P wave duration (observable entity) PMID 24850809 2014 Genetic determinants of P wave duration and PR segment.

rs6801957 in SCN10A gene and QRS complex feature PMID 27659466 2016 52 Genetic Loci Influencing Myocardial Mass.

rs6801957 in SCN10A 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.

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