{{Rsnum
|rsid=12063142
|Chromosome=1
|position=18813023
|Orientation=plus
|GMAF=0.2052
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 57.5 | 37.2 | 5.3
| HCB | 90.5 | 9.5 | 0.0
| JPT | 95.6 | 4.4 | 0.0
| YRI | 58.5 | 36.7 | 4.8
| ASW | 54.4 | 35.1 | 10.5
| CHB | 90.5 | 9.5 | 0.0
| CHD | 95.4 | 4.6 | 0.0
| GIH | 35.6 | 51.5 | 12.9
| LWK | 66.1 | 28.4 | 5.5
| MEX | 43.1 | 53.4 | 3.4
| MKK | 0.0 | 0.0 | 0.0
| TSI | 59.8 | 30.4 | 9.8
| 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=
|Pval=5E-7
|OR=None
|ORtxt=None
|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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}