{{Rsnum
|rsid=1352075
|Gene=CCND1
|Chromosome=11
|position=69642525
|Orientation=plus
|GMAF=0.4986
|Gene_s=CCND1,LOC100996515
|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 | 27.4 | 41.6 | 31.0
| HCB | 4.4 | 26.5 | 69.1
| JPT | 1.8 | 35.7 | 62.5
| YRI | 59.7 | 36.1 | 4.2
| ASW | 50.0 | 44.6 | 5.4
| CHB | 4.4 | 26.5 | 69.1
| CHD | 0.9 | 30.3 | 68.8
| GIH | 14.0 | 44.0 | 42.0
| LWK | 55.0 | 43.1 | 1.8
| MEX | 35.7 | 44.6 | 19.6
| MKK | 56.8 | 40.0 | 3.2
| TSI | 21.6 | 52.0 | 26.5
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23502783
  |Trait=Multiple myeloma (hyperdiploidy)
  |Title=The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
  |RiskAllele=A
  |Pval=2E-6
  |OR=1.42
  |ORtxt=[1.23-1.64]
  }}

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