{{Rsnum
|rsid=7086888
|Chromosome=10
|position=4676196
|Orientation=plus
|GMAF=0.1047
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 83.2 | 16.8 | 0.0
| HCB | 99.3 | 0.7 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 47.6 | 41.5 | 10.9
| ASW | 52.6 | 43.9 | 3.5
| CHB | 99.3 | 0.7 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 78.2 | 18.8 | 3.0
| LWK | 48.2 | 45.5 | 6.4
| MEX | 93.1 | 6.9 | 0.0
| MKK | 47.4 | 38.5 | 14.1
| TSI | 89.2 | 9.8 | 1.0
| 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=8E-6
  |OR=1.87
  |ORtxt=[1.42-2.46]
  }}

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