{{Rsnum
|rsid=1449572
|Chromosome=13
|position=48892795
|Orientation=minus
|GMAF=0.1882
|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 | 0.0 | 28.3 | 71.7
| HCB | 6.6 | 29.2 | 64.2
| JPT | 4.4 | 38.9 | 56.6
| YRI | 2.0 | 25.2 | 72.8
| ASW | 0.0 | 29.8 | 70.2
| CHB | 6.6 | 29.2 | 64.2
| CHD | 5.5 | 38.5 | 56.0
| GIH | 0.0 | 23.8 | 76.2
| LWK | 1.8 | 10.9 | 87.3
| MEX | 13.8 | 46.6 | 39.7
| MKK | 0.6 | 19.2 | 80.1
| TSI | 2.0 | 28.4 | 69.6
| 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=A
  |Pval=8E-6
  |OR=1.73
  |ORtxt=[1.36-2.21]
  }}

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