{{Rsnum
|rsid=10464059
|Chromosome=5
|position=180367208
|Orientation=plus
|GMAF=0.2277
|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 | 0.9 | 26.8 | 72.3
| HCB | 14.6 | 50.4 | 35.0
| JPT | 8.8 | 46.0 | 45.1
| YRI | 10.9 | 42.9 | 46.3
| ASW | 15.8 | 36.8 | 47.4
| CHB | 14.6 | 50.4 | 35.0
| CHD | 12.8 | 46.8 | 40.4
| GIH | 7.9 | 34.7 | 57.4
| LWK | 10.0 | 44.5 | 45.5
| MEX | 0.0 | 25.9 | 74.1
| MKK | 7.7 | 47.1 | 45.2
| TSI | 0.0 | 20.6 | 79.4
| 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=A
|Pval=0.000003
|OR=1.33
|ORtxt=[1.19-1.52]
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}