{{Rsnum
|rsid=523516
|Gene=CACNB1
|Chromosome=17
|position=39175092
|Orientation=plus
|GMAF=0.213
|Gene_s=CACNB1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 63.1 | 35.4 | 1.5
| HCB | 46.2 | 46.2 | 7.7
| JPT | 72.1 | 27.9 | 0.0
| YRI | 39.3 | 50.0 | 10.7
| ASW | 0.0 | 0.0 | 0.0
| CHB | 46.2 | 46.2 | 7.7
| 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 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=T
  |Pval=4E-6
  |OR=.19
  |ORtxt=[0.11-0.27] unit decrease
  |OA=1
}}

{{on chip | HumanOmni1Quad}}