{{Rsnum
|rsid=12545912
|Gene=TNKS
|Chromosome=8
|position=9744189
|Orientation=plus
|GMAF=0.2718
|Gene_s=TNKS
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 3.5 | 38.1 | 58.4
| HCB | 4.4 | 45.3 | 50.4
| JPT | 6.2 | 33.6 | 60.2
| YRI | 11.6 | 47.9 | 40.4
| ASW | 5.3 | 43.9 | 50.9
| CHB | 4.4 | 45.3 | 50.4
| CHD | 4.7 | 43.9 | 51.4
| GIH | 5.9 | 43.6 | 50.5
| LWK | 17.6 | 50.9 | 31.5
| MEX | 1.7 | 29.3 | 69.0
| MKK | 16.7 | 51.3 | 32.1
| TSI | 2.9 | 26.5 | 70.6
| 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=C
  |Pval=7E-6
  |OR=1.30
  |ORtxt=[1.16-1.45]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}