{{Rsnum
|rsid=6601327
|Chromosome=8
|position=9538022
|Orientation=plus
|GMAF=0.4885
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 37.2 | 49.6 | 13.3
| HCB | 14.1 | 44.4 | 41.5
| JPT | 17.7 | 46.9 | 35.4
| YRI | 27.2 | 44.9 | 27.9
| ASW | 33.3 | 50.9 | 15.8
| CHB | 14.1 | 44.4 | 41.5
| CHD | 13.9 | 44.4 | 41.7
| GIH | 34.7 | 47.5 | 17.8
| LWK | 20.9 | 41.8 | 37.3
| MEX | 21.1 | 50.9 | 28.1
| MKK | 29.7 | 50.3 | 20.0
| TSI | 52.0 | 38.2 | 9.8
| 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=G
  |Pval=8E-6
  |OR=1.27
  |ORtxt=[1.14-1.41]
  }}

{{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}}