{{Rsnum
|rsid=11248060
|Gene=DGKQ
|Chromosome=4
|position=970571
|Orientation=plus
|GMAF=0.08678
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=DGKQ
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 75.2 | 24.8 | 0.0
| HCB | 88.3 | 10.9 | 0.7
| JPT | 73.2 | 25.9 | 0.9
| YRI | 96.6 | 3.4 | 0.0
| ASW | 93.0 | 7.0 | 0.0
| CHB | 88.3 | 10.9 | 0.7
| CHD | 81.5 | 18.5 | 0.0
| GIH | 54.5 | 37.6 | 7.9
| LWK | 96.4 | 3.6 | 0.0
| MEX | 91.4 | 8.6 | 0.0
| MKK | 82.7 | 17.3 | 0.0
| TSI | 76.5 | 22.5 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20070850
|Trait=Parkinson's disease
|Title=Genome-Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease
|RiskAllele=
|Pval=0.000002
|OR=None
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=22451204
|Title=Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2
|OA=1
}}

{{PMID Auto GWAS
|PMID=22438815
|Trait=None
|Title=Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
|RiskAllele=
|Pval=3E-12
|OR=1.2100
|ORtxt=None
|OA=1
}}

{{PMID|18985386|OA=1
}} Genomewide association study for susceptibility genes contributing to familial Parkinson disease.

{{PMID|21281506|OA=1
}} A unified framework for multi-locus association analysis of both common and rare variants.

{{PMID Auto
|PMID=23618683
|Title=GAK rs1564282 and DGKQ rs11248060 increase the risk for Parkinson's disease in a Chinese population.
}}

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