{{Rsnum
|rsid=6801957
|Gene=SCN10A
|Chromosome=3
|position=38725824
|Orientation=plus
|GMAF=0.3049
|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 | 29.7 | 56.2 | 14.1
| HCB | 60.0 | 33.3 | 6.7
| JPT | 53.3 | 44.4 | 2.2
| YRI | 80.3 | 19.7 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 60.0 | 33.3 | 6.7
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21076409
|Trait=None
|Title=Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
|RiskAllele=T
|Pval=3E-14
|OR=0.5400
|ORtxt=[NR] ms increase
|OA=1
}}

{{PMID Auto GWAS
  |PMID=23139255
  |Trait=PR interval
  |Title=Novel Loci Associated With PR Interval in a Genome-Wide Association Study of 10 African American Cohorts.
  |RiskAllele=T
  |Pval=9E-9
  |OR=3.36
  |ORtxt=[2.22-4.50] unit increase
  |OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}