{{Rsnum
|rsid=11026318
|Chromosome=11
|position=21875334
|Orientation=plus
|GMAF=0.1993
|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 | 79.6 | 17.7 | 2.7
| HCB | 67.9 | 24.1 | 8.0
| JPT | 71.7 | 28.3 | 0.0
| YRI | 42.9 | 44.2 | 12.9
| ASW | 49.1 | 38.6 | 12.3
| CHB | 67.9 | 24.1 | 8.0
| CHD | 53.7 | 42.6 | 3.7
| GIH | 76.2 | 18.8 | 5.0
| LWK | 38.2 | 49.1 | 12.7
| MEX | 56.9 | 37.9 | 5.2
| MKK | 56.4 | 39.1 | 4.5
| TSI | 82.2 | 15.8 | 2.0
| 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=9E-6
  |OR=2.33
  |ORtxt=[1.60-3.38]
  }}

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