{{Rsnum
|rsid=6800541
|Gene=SCN10A
|Chromosome=3
|position=38733341
|Orientation=plus
|GMAF=0.259
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SCN10A
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 14.2 | 55.8 | 30.1
| HCB | 2.2 | 22.6 | 75.2
| JPT | 4.4 | 29.2 | 66.4
| YRI | 0.0 | 1.4 | 98.6
| ASW | 3.5 | 15.8 | 80.7
| CHB | 2.2 | 22.6 | 75.2
| CHD | 2.8 | 22.0 | 75.2
| GIH | 10.9 | 50.5 | 38.6
| LWK | 0.0 | 10.9 | 89.1
| MEX | 8.6 | 41.4 | 50.0
| MKK | 0.6 | 19.2 | 80.1
| TSI | 16.7 | 47.1 | 36.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20062060
|Trait=PR interval
|Title=Genome-wide association study of PR interval
|RiskAllele=C
|Pval=2E-74
|OR=3.77
|ORtxt=[3.37-4.17] ms increase
|OA=1
}}

{{PMID Auto GWAS
|PMID=21041692
|Trait=None
|Title=Identification of Genomic Predictors of Atrioventricular Conduction. Using Electronic Medical Records as a Tool for Genome Science
|RiskAllele=C
|Pval=5E-7
|OR=2.6000
|ORtxt=[1.62-3.70] ms increase
|OA=1
}}

{{PMID Auto
|PMID=23092954
|Title=SHAVE: shrinkage estimator measured for multiple visits increases power in GWAS of quantitative traits.
|OA=1
}}

{{PMID Auto
|PMID=25085921
|Title=Common and Rare Variants in SCN10A Modulate the Risk of Atrial Fibrillation
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}