{{Rsnum
|rsid=780179
|Gene=CDH12
|Chromosome=5
|position=22812155
|Orientation=plus
|GMAF=0.4995
|Gene_s=CDH12
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 21.6 | 57.7 | 20.7
| HCB | 10.6 | 42.4 | 47.0
| JPT | 20.0 | 40.0 | 40.0
| YRI | 42.9 | 44.4 | 12.7
| ASW | 28.3 | 41.5 | 30.2
| CHB | 10.6 | 42.4 | 47.0
| CHD | 10.3 | 43.0 | 46.7
| GIH | 30.3 | 42.4 | 27.3
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 38.6 | 47.1 | 14.4
| TSI | 22.7 | 56.7 | 20.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23502783
  |Trait=Multiple myeloma (IgH translocation)
  |Title=The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
  |RiskAllele=G
  |Pval=9E-7
  |OR=1.59
  |ORtxt=[1.32-1.92]
  }}

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