|| common in clinvar
|?|| (A;A) (A;G) (G;G) ||28|
] Genetic variation in SCN10A influences cardiac conduction
[PMID 21041692] Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science
[PMID 20062060] Genome-wide association study of PR interval.
[PMID 21347284] Genome-wide association studies of the PR interval in African Americans.
|| not reviewed
|| Insufficiently evaluated not reviewed
[PMID 24072447] Common SCN10A variants modulate PR interval and heart rate response during atrial fibrillation
[PMID 23092954] SHAVE: shrinkage estimator measured for multiple visits increases power in GWAS of quantitative traits.
[PMID 25085921] Common and Rare Variants in SCN10A Modulate the Risk of Atrial Fibrillation
[PMID 25691686] Common and Rare Variants in SCN10A Modulate the Risk of Atrial Fibrillation
[PMID 25691538] Role of common and rare variants in SCN10A: Results from the Brugada syndrome QRS locus gene discovery collaborative study
[PMID 26104176] Association Between Genetic Variation in the SCN10A Gene and Cardiac Conduction Abnormalities in Patients With Hypertrophic Cardiomyopathy