{{Rsnum
|rsid=626657
|Gene=CACNB1
|Chromosome=17
|position=39176710
|Orientation=plus
|GMAF=0.2571
|Gene_s=CACNB1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.9 | 23.9 | 75.2
| HCB | 2.9 | 47.4 | 49.6
| JPT | 0.9 | 30.1 | 69.0
| YRI | 40.8 | 45.6 | 13.6
| ASW | 29.8 | 45.6 | 24.6
| CHB | 2.9 | 47.4 | 49.6
| CHD | 7.3 | 31.2 | 61.5
| GIH | 1.0 | 15.8 | 83.2
| LWK | 29.1 | 51.8 | 19.1
| MEX | 3.4 | 10.3 | 86.2
| MKK | 18.2 | 55.8 | 26.0
| TSI | 2.9 | 23.5 | 73.5
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23382691
  |Trait=IgG glycosylation
  |Title=Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
  |RiskAllele=C
  |Pval=2E-6
  |OR=.23
  |ORtxt=[0.14-0.33] unit decrease
  |OA=1
}}

{{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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}