{{Rsnum
|rsid=10180663
|Gene=DTNB
|Chromosome=2
|position=25410373
|Orientation=plus
|GMAF=0.472
|Gene_s=DTNB
|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 | 6.2 | 39.8 | 54.0
| HCB | 41.6 | 48.2 | 10.2
| JPT | 31.9 | 54.0 | 14.2
| YRI | 74.1 | 22.4 | 3.4
| ASW | 68.4 | 26.3 | 5.3
| CHB | 41.6 | 48.2 | 10.2
| CHD | 36.7 | 52.3 | 11.0
| GIH | 9.9 | 40.6 | 49.5
| LWK | 73.4 | 26.6 | 0.0
| MEX | 10.3 | 53.4 | 36.2
| MKK | 59.4 | 38.1 | 2.6
| TSI | 11.8 | 40.2 | 48.0
| 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=A
  |Pval=2E-6
  |OR=1.64
  |ORtxt=[1.34-2.02]
  }}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}