{{Rsnum
|rsid=8099213
|Chromosome=18
|position=67284976
|Orientation=plus
|GMAF=0.494
|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 | 42.3 | 43.2 | 14.4
| HCB | 2.2 | 30.1 | 67.6
| JPT | 3.5 | 36.3 | 60.2
| YRI | 22.1 | 53.1 | 24.8
| ASW | 35.1 | 42.1 | 22.8
| CHB | 2.2 | 30.1 | 67.6
| CHD | 6.5 | 29.6 | 63.9
| GIH | 14.9 | 50.5 | 34.7
| LWK | 35.8 | 46.8 | 17.4
| MEX | 37.9 | 51.7 | 10.3
| MKK | 39.1 | 51.3 | 9.6
| TSI | 32.3 | 53.5 | 14.1
| 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=5E-6
  |OR=1.52
  |ORtxt=[1.27-1.81]
  }}

{{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}}