{{Rsnum
|rsid=7577599
|Gene=DTNB
|Chromosome=2
|position=25390277
|Orientation=plus
|GMAF=0.3613
|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 | 25.7 | 68.1
| HCB | 39.3 | 50.4 | 10.4
| JPT | 30.9 | 55.5 | 13.6
| YRI | 18.2 | 46.9 | 35.0
| ASW | 14.3 | 42.9 | 42.9
| CHB | 39.3 | 50.4 | 10.4
| CHD | 30.5 | 58.1 | 11.4
| GIH | 5.0 | 29.7 | 65.3
| LWK | 0.0 | 0.0 | 0.0
| MEX | 5.3 | 50.9 | 43.9
| MKK | 9.1 | 35.1 | 55.8
| TSI | 3.0 | 27.3 | 69.7
| 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=6E-6
  |OR=1.43
  |ORtxt=[1.22-1.67]
  }}

{{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}}