{{Rsnum
|rsid=11890028
|Gene=SCN1A
|Chromosome=2
|position=166086767
|Orientation=plus
|GMAF=0.1974
|Gene_s=SCN1A
|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 | 9.7 | 39.8 | 50.4
| HCB | 2.2 | 24.3 | 73.5
| JPT | 0.0 | 15.0 | 85.0
| YRI | 4.8 | 23.8 | 71.4
| ASW | 0.0 | 24.6 | 75.4
| CHB | 2.2 | 24.3 | 73.5
| CHD | 2.8 | 17.4 | 79.8
| GIH | 7.9 | 40.6 | 51.5
| LWK | 0.0 | 15.5 | 84.5
| MEX | 5.2 | 34.5 | 60.3
| MKK | 3.2 | 27.1 | 69.7
| TSI | 13.7 | 46.1 | 40.2
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22949513
  |Trait=Epilepsy (generalized)
  |Title=Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32
  |RiskAllele=T
  |Pval=4E-6
  |OR=1.18
  |ORtxt=[1.09-1.27]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}