{{Rsnum
|rsid=289585
|Gene=DLC1
|Chromosome=8
|position=13403027
|Orientation=minus
|GMAF=0.101
|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 | 70.8 | 26.5 | 2.7
| HCB | 97.8 | 2.2 | 0.0
| JPT | 94.7 | 5.3 | 0.0
| YRI | 75.5 | 24.5 | 0.0
| ASW | 75.4 | 24.6 | 0.0
| CHB | 97.8 | 2.2 | 0.0
| CHD | 94.5 | 5.5 | 0.0
| GIH | 58.4 | 37.6 | 4.0
| LWK | 76.4 | 20.9 | 2.7
| MEX | 89.7 | 10.3 | 0.0
| MKK | 62.8 | 30.1 | 7.1
| TSI | 73.5 | 25.5 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22688191
|Trait=None
|Title=Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
|RiskAllele=
|Pval=0.000005
|OR=1.4500
|ORtxt=None
|OA=1
}}

{{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}}
{{on chip | NatGeo2}}