{{Rsnum
|rsid=139371
|Chromosome=22
|position=39123191
|Orientation=plus
|GMAF=0.4853
|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 | 19.5 | 52.2 | 28.3
| HCB | 13.2 | 47.1 | 39.7
| JPT | 10.6 | 32.7 | 56.6
| YRI | 90.5 | 9.5 | 0.0
| ASW | 63.2 | 35.1 | 1.8
| CHB | 13.2 | 47.1 | 39.7
| CHD | 13.8 | 45.9 | 40.4
| GIH | 16.8 | 53.5 | 29.7
| LWK | 94.5 | 5.5 | 0.0
| MEX | 10.3 | 44.8 | 44.8
| MKK | 76.1 | 21.9 | 1.9
| TSI | 13.7 | 50.0 | 36.3
| 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=9E-6
  |OR=1.50
  |ORtxt=[1.26-1.80]
  }}

{{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}}