{{Rsnum
|rsid=6800901
|Gene=POLQ
|Chromosome=3
|position=121435346
|Orientation=plus
|GMAF=0.2084
|Gene_s=POLQ
|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 | 49.6 | 39.8 | 10.6
| HCB | 72.3 | 24.1 | 3.6
| JPT | 78.2 | 17.3 | 4.5
| YRI | 83.0 | 17.0 | 0.0
| ASW | 70.2 | 28.1 | 1.8
| CHB | 72.3 | 24.1 | 3.6
| CHD | 70.6 | 26.6 | 2.8
| GIH | 62.4 | 25.7 | 11.9
| LWK | 79.1 | 19.1 | 1.8
| MEX | 63.8 | 31.0 | 5.2
| MKK | 78.8 | 19.2 | 1.9
| TSI | 41.0 | 53.0 | 6.0
| 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=1.31
  |ORtxt=[1.17-1.47]
  }}

{{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}}