{{Rsnum
|rsid=12659144
|Chromosome=5
|position=174350517
|Orientation=plus
|GMAF=0.2236
|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 | 6.2 | 24.8 | 69.0
| HCB | 4.4 | 52.6 | 43.1
| JPT | 6.2 | 33.6 | 60.2
| YRI | 5.4 | 38.8 | 55.8
| ASW | 7.0 | 43.9 | 49.1
| CHB | 4.4 | 52.6 | 43.1
| CHD | 10.1 | 45.9 | 44.0
| GIH | 0.0 | 27.7 | 72.3
| LWK | 16.4 | 48.2 | 35.5
| MEX | 3.4 | 22.4 | 74.1
| MKK | 10.9 | 43.6 | 45.5
| TSI | 2.0 | 32.4 | 65.7
| 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=G
  |Pval=3E-6
  |OR=1.67
  |ORtxt=[1.35-2.07]
  }}

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