{{Rsnum
|rsid=11157317
|Chromosome=14
|position=42934256
|Orientation=plus
|GMAF=0.2897
|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 | 60.2 | 34.5 | 5.3
| HCB | 39.4 | 46.0 | 14.6
| JPT | 45.1 | 43.4 | 11.5
| YRI | 64.6 | 32.0 | 3.4
| ASW | 73.2 | 25.0 | 1.8
| CHB | 39.4 | 46.0 | 14.6
| CHD | 38.9 | 51.9 | 9.3
| GIH | 67.3 | 28.7 | 4.0
| LWK | 56.4 | 40.0 | 3.6
| MEX | 37.9 | 39.7 | 22.4
| MKK | 53.8 | 43.6 | 2.6
| TSI | 58.8 | 32.4 | 8.8
| 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=A
  |Pval=9E-6
  |OR=1.29
  |ORtxt=[1.15-1.44]
  }}

{{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}}