{{Rsnum
|rsid=4521323
|Chromosome=4
|position=173734763
|Orientation=plus
|GMAF=0.4275
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=LOC101928478
|Gene_s=LOC101928478
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 15.9 | 53.1 | 31.0
| HCB | 10.2 | 30.7 | 59.1
| JPT | 3.5 | 34.5 | 61.9
| YRI | 39.0 | 50.0 | 11.0
| ASW | 45.6 | 45.6 | 8.8
| CHB | 10.2 | 30.7 | 59.1
| CHD | 5.5 | 34.9 | 59.6
| GIH | 14.9 | 54.5 | 30.7
| LWK | 38.2 | 50.9 | 10.9
| MEX | 5.2 | 51.7 | 43.1
| MKK | 51.3 | 35.3 | 13.5
| TSI | 20.6 | 49.0 | 30.4
| 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=C
  |Pval=9E-6
  |OR=1.28
  |ORtxt=[1.15-1.43]
  }}

{{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}}