{{Rsnum
|rsid=10200894
|Chromosome=2
|position=227952416
|Orientation=plus
|GMAF=0.1754
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 86.7 | 11.5 | 1.8
| HCB | 40.9 | 46.0 | 13.1
| JPT | 54.5 | 38.4 | 7.1
| YRI | 69.4 | 29.3 | 1.4
| ASW | 57.9 | 40.4 | 1.8
| CHB | 40.9 | 46.0 | 13.1
| CHD | 38.9 | 48.1 | 13.0
| GIH | 84.2 | 14.9 | 1.0
| LWK | 76.1 | 23.9 | 0.0
| MEX | 59.6 | 36.8 | 3.5
| MKK | 86.4 | 13.6 | 0.0
| TSI | 85.1 | 14.9 | 0.0
| HapMapRevision=28
}}{{Report GE
|PubMed=16252231
|Source=pubmed
|AffyProbeset=SNP_A-8385601
|AffyOrientation=same
|AlleleA=C
|AlleleB=G
|onGW5=
|rsid=10200894
|ancestral=C
|RiskPopulation=
|RiskAllele=C
|CaseFreq=0.93
|ControlFreq=0.87
|OddsRatioHet=
|OddsRatioHom=
|OddsRatioAll=1.84
|Disease=Parkinson's disease
|DiseaseSymbol=PKD
|OA=1
}}

rs10200894 increases susceptibility to Parkinson's disease 1.84 times for carriers of the C allele {{PMID|16252231|OA=1
}}

{{PMID Auto
|PMID=16685661
|Title=Genomewide association, Parkinson disease, and PARK10.
|OA=1
}}

{{PMID Auto
|PMID=16685662
|Title=No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.
|OA=1
}}

{{PMID Auto
|PMID=16685663
|Title=A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.
|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}}