{{Rsnum
|rsid=602594
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=11
|position=118169895
|Orientation=minus
|Gene=SCN2B
|Gene_s=SCN2B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 12.3 | 87.7
| HCB | 0.0 | 29.5 | 70.5
| JPT | 4.5 | 36.4 | 59.1
| YRI | 50.0 | 45.2 | 4.8
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 29.5 | 70.5
| 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
}}