{{Rsnum
|rsid=8056064
|Gene=CDH13
|Chromosome=16
|position=82753448
|Orientation=plus
|GMAF=0.2323
|Gene_s=CDH13
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 62.8 | 33.6 | 3.5
| HCB | 27.7 | 50.4 | 21.9
| JPT | 26.8 | 50.9 | 22.3
| YRI | 76.9 | 23.1 | 0.0
| ASW | 84.2 | 12.3 | 3.5
| CHB | 27.7 | 50.4 | 21.9
| CHD | 29.9 | 43.9 | 26.2
| GIH | 58.4 | 36.6 | 5.0
| LWK | 65.5 | 33.6 | 0.9
| MEX | 69.0 | 29.3 | 1.7
| MKK | 60.3 | 34.0 | 5.8
| TSI | 64.7 | 30.4 | 4.9
| 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=2E-6
  |OR=1.68
  |ORtxt=[1.36-2.08]
  }}

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