{{Rsnum
|rsid=12541254
|Gene=DLC1
|Chromosome=8
|position=13121891
|Orientation=plus
|GMAF=0.2778
|Gene_s=DLC1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 15.9 | 42.5 | 41.6
| HCB | 1.5 | 14.6 | 83.9
| JPT | 0.9 | 17.9 | 81.2
| YRI | 32.0 | 49.0 | 19.0
| ASW | 22.8 | 35.1 | 42.1
| CHB | 1.5 | 14.6 | 83.9
| CHD | 2.8 | 19.4 | 77.8
| GIH | 10.9 | 45.5 | 43.6
| LWK | 20.2 | 51.4 | 28.4
| MEX | 3.4 | 37.9 | 58.6
| MKK | 17.4 | 46.5 | 36.1
| TSI | 12.7 | 47.1 | 40.2
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23509962
  |Trait=Venous thromboembolism (gene x gene interaction)
  |Title=A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.
  |RiskAllele=A
  |Pval=3E-9
  |OR=1.65
  |ORtxt=[NR]
  |OA=1
}}

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