{{Rsnum
|rsid=35866326
|Chromosome=10
|position=59316923
|Orientation=plus
|GMAF=0.1685
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 83.2 | 15.9 | 0.9
| HCB | 67.2 | 29.2 | 3.6
| JPT | 53.1 | 39.8 | 7.1
| YRI | 63.3 | 28.6 | 8.2
| ASW | 73.7 | 24.6 | 1.8
| CHB | 67.2 | 29.2 | 3.6
| CHD | 72.5 | 23.9 | 3.7
| GIH | 50.5 | 45.5 | 4.0
| LWK | 62.7 | 32.7 | 4.5
| MEX | 50.0 | 46.6 | 3.4
| MKK | 48.7 | 41.0 | 10.3
| TSI | 78.4 | 20.6 | 1.0
| HapMapRevision=28
}}

{{Report GE
|PubMed=16252231
|Source=pubmed
|AffyProbeset=SNP_A-2127493
|AffyOrientation=reverse
|AlleleA=C
|AlleleB=G
|onGW5=
|rsid=35866326
|ancestral=
|RiskPopulation=
|RiskAllele=C
|CaseFreq=0.93
|ControlFreq=0.89
|OddsRatioHet=
|OddsRatioHom=
|OddsRatioAll=1.88
|Disease=Parkinson's disease
|DiseaseSymbol=PKD
|OA=1
}}

rs35866326 increases susceptibility to Parkinson's disease 1.88 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 | Affy500k}}
{{on chip | HumanOmni1Quad}}