{{Rsnum
|rsid=10740993
|Gene=CACNB2
|Chromosome=10
|position=18442482
|Orientation=plus
|GMAF=0.4757
|Gene_s=CACNB2
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 30.1 | 54.9 | 15.0
| HCB | 16.8 | 43.8 | 39.4
| JPT | 21.2 | 55.8 | 23.0
| YRI | 12.2 | 46.9 | 40.8
| ASW | 19.3 | 49.1 | 31.6
| CHB | 16.8 | 43.8 | 39.4
| CHD | 16.5 | 49.5 | 33.9
| GIH | 31.7 | 47.5 | 20.8
| LWK | 12.7 | 46.4 | 40.9
| MEX | 34.5 | 50.0 | 15.5
| MKK | 11.5 | 47.4 | 41.0
| TSI | 21.6 | 52.0 | 26.5
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23704328
  |Trait=Primary tooth development (number of teeth)
  |Title=Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.
  |RiskAllele=C
  |Pval=2E-9
  |OR=.14
  |ORtxt=[0.096-0.186] unit increase
  |OA=1
}}

{{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}}