Variant: rs6795970 

    present in Gene: SCN10A
    present in Chromosome: 3
    Position on Chromosome: 38725184
    Alleles of this Variant: A/G

rs6795970 in SCN10A 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.

rs6795970 in SCN10A gene and Electrocardiogram: P-R interval PMID 21347284 2011 Genome-wide association studies of the PR interval in African Americans.

PMID 20062063 2010 Several common variants modulate heart rate, PR interval and QRS duration.

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

PMID 20062061 2010 Replication testing among 6,243 Indian Asians and 5,370 Europeans confirmed that rs6795970 (G>A) is associated with prolonged cardiac conduction (longer P-wave duration, PR interval and QRS duration, P = 10(-5) to 10(-20)).

rs6795970 in SCN10A gene and Electrocardiography PMID 20062061 2010 Genetic variation in SCN10A influences cardiac conduction.

rs6795970 in SCN10A gene and QRS complex feature PMID 20062063 2010 Several common variants modulate heart rate, PR interval and QRS duration.

PMID 27659466 2016 52 Genetic Loci Influencing Myocardial Mass.