{{Rsnum
|rsid=11013860
|Chromosome=10
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=CACNB2
|position=18654027
|Gene_s=CACNB2
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 88.5 | 10.6 | 0.9
| HCB | 16.9 | 47.8 | 35.3
| JPT | 22.1 | 51.3 | 26.5
| YRI | 77.6 | 20.4 | 2.0
| ASW | 75.4 | 22.8 | 1.8
| CHB | 16.9 | 47.8 | 35.3
| CHD | 22.0 | 46.8 | 31.2
| GIH | 57.4 | 36.6 | 5.9
| LWK | 82.6 | 17.4 | 0.0
| MEX | 94.8 | 5.2 | 0.0
| MKK | 75.3 | 23.4 | 1.3
| TSI | 87.3 | 12.7 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=24581832
|Title=Exploring the associations between genetic variants in genes encoding for subunits of calcium channel and subtypes of bipolar disorder
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}