{{Rsnum
|rsid=10428132
|Gene=SCN10A
|Chromosome=3
|position=38736063
|Orientation=plus
|GMAF=0.2957
|Gene_s=SCN10A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 30.1 | 55.8 | 14.2
| HCB | 64.2 | 32.1 | 3.6
| JPT | 56.6 | 38.1 | 5.3
| YRI | 91.8 | 8.2 | 0.0
| ASW | 64.9 | 31.6 | 3.5
| CHB | 64.2 | 32.1 | 3.6
| CHD | 69.7 | 26.6 | 3.7
| GIH | 36.6 | 51.5 | 11.9
| LWK | 75.5 | 21.8 | 2.7
| MEX | 36.2 | 53.4 | 10.3
| MKK | 76.3 | 22.4 | 1.3
| TSI | 36.3 | 47.1 | 16.7
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23872634
  |Trait=Brugada syndrome
  |Title=Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
  |RiskAllele=T
  |Pval=1E-68
  |OR=2.55
  |ORtxt=[2.30-2.84]
  }}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}