{{Rsnum
|rsid=12467383
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=2
|position=165369259
|Orientation=plus
|Gene=SCN2A
|Gene_s=SCN2A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 4.7 | 32.8 | 62.5
| HCB | 17.8 | 35.6 | 46.7
| JPT | 11.1 | 31.1 | 57.8
| YRI | 1.6 | 1.6 | 96.7
| ASW | 0.0 | 0.0 | 0.0
| CHB | 17.8 | 35.6 | 46.7
| 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
|PMID=24337656
|Title=Case-control association study of polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, SCN3A, SCN1B, and SCN2B and epilepsy
}}