{{Rsnum
|rsid=11248051
|Gene=GAK
|Chromosome=4
|position=864544
|Orientation=plus
|GMAF=0.08448
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=GAK
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 77.9 | 22.1 | 0.0
| HCB | 89.6 | 10.4 | 0.0
| JPT | 77.0 | 22.1 | 0.9
| YRI | 99.3 | 0.7 | 0.0
| ASW | 94.7 | 5.3 | 0.0
| CHB | 89.6 | 10.4 | 0.0
| CHD | 83.3 | 16.7 | 0.0
| GIH | 62.4 | 31.7 | 5.9
| LWK | 98.2 | 1.8 | 0.0
| MEX | 93.1 | 6.9 | 0.0
| MKK | 87.7 | 12.3 | 0.0
| TSI | 75.5 | 23.5 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20711177
|Trait=None
|Title=Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease
|RiskAllele=T
|Pval=3E-9
|OR=1.46
|ORtxt=[1.29-1.65]
|OA=1
}}

{{omim
|id=168600
|rsnum=11248051
}}

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

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

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

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}