{{Rsnum
|rsid=2823357
|Chromosome=21
|position=15542586
|Orientation=plus
|GMAF=0.4601
|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 | 47.8 | 36.3
| HCB | 8.8 | 39.4 | 51.8
| JPT | 11.5 | 38.9 | 49.6
| YRI | 61.9 | 30.6 | 7.5
| ASW | 49.1 | 38.6 | 12.3
| CHB | 8.8 | 39.4 | 51.8
| CHD | 11.9 | 43.1 | 45.0
| GIH | 21.0 | 48.0 | 31.0
| LWK | 59.1 | 33.6 | 7.3
| MEX | 17.2 | 53.4 | 29.3
| MKK | 64.1 | 30.1 | 5.8
| TSI | 11.8 | 37.3 | 51.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21738487
|Trait=None
|Title=Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease.
|RiskAllele=A
|Pval=6E-7
|OR=1.1500
|ORtxt=[1.09-1.21]
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}