{{Rsnum
|rsid=7144018
|Chromosome=14
|position=57140349
|Orientation=plus
|GMAF=0.258
|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 | 0.9 | 16.8 | 82.3
| HCB | 0.0 | 13.2 | 86.8
| JPT | 0.0 | 8.0 | 92.0
| YRI | 72.8 | 26.5 | 0.7
| ASW | 56.1 | 38.6 | 5.3
| CHB | 0.0 | 13.2 | 86.8
| CHD | 0.9 | 16.5 | 82.6
| GIH | 1.0 | 20.8 | 78.2
| LWK | 74.1 | 23.1 | 2.8
| MEX | 0.0 | 20.7 | 79.3
| MKK | 39.1 | 44.2 | 16.7
| TSI | 1.0 | 22.8 | 76.2
| 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=1.85
  |ORtxt=[1.41-2.44]
  }}

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