{{Rsnum
|rsid=11978472
|Gene=CACNA2D1
|Chromosome=7
|position=82210237
|Orientation=plus
|GMAF=0.3691
|Gene_s=CACNA2D1
|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 | 33.6 | 42.5 | 23.9
| HCB | 23.1 | 51.5 | 25.4
| JPT | 29.4 | 37.6 | 33.0
| YRI | 85.0 | 14.3 | 0.7
| ASW | 87.7 | 12.3 | 0.0
| CHB | 23.1 | 51.5 | 25.4
| CHD | 18.5 | 55.6 | 25.9
| GIH | 37.0 | 50.0 | 13.0
| LWK | 72.5 | 27.5 | 0.0
| MEX | 33.9 | 48.2 | 17.9
| MKK | 82.7 | 16.0 | 1.3
| TSI | 38.6 | 42.6 | 18.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23665963
  |Trait=Crohn's disease (need for surgery)
  |Title=Multidimensional prognostic risk assessment identifies association between IL12B variation and surgery in Crohn's disease.
  |RiskAllele=
  |Pval=6E-6
  |OR=2.00
  |ORtxt=[1.43-2.50]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}