{{Rsnum
|rsid=9388451
|Chromosome=6
|position=125769231
|Orientation=plus
|GMAF=0.4605
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 23.9 | 45.1 | 31.0
| HCB | 54.7 | 39.4 | 5.8
| JPT | 30.1 | 48.7 | 21.2
| YRI | 0.7 | 17.7 | 81.6
| ASW | 0.0 | 33.3 | 66.7
| CHB | 54.7 | 39.4 | 5.8
| CHD | 53.2 | 39.4 | 7.3
| GIH | 14.9 | 47.5 | 37.6
| LWK | 1.8 | 21.8 | 76.4
| MEX | 36.2 | 44.8 | 19.0
| MKK | 4.5 | 30.1 | 65.4
| TSI | 21.6 | 50.0 | 28.4
| 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=C
  |Pval=5E-17
  |OR=1.58
  |ORtxt=[1.42-1.75]
  }}

{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA}}