{{Rsnum
|rsid=3775442
|Gene=SNCA
|Chromosome=4
|position=89794080
|Orientation=plus
|GMAF=0.1552
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SNCA
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 95.6 | 4.4 | 0.0
| HCB | 46.0 | 44.5 | 9.5
| JPT | 42.5 | 42.5 | 15.0
| YRI | 72.6 | 25.3 | 2.1
| ASW | 71.4 | 25.0 | 3.6
| CHB | 46.0 | 44.5 | 9.5
| CHD | 33.9 | 55.0 | 11.0
| GIH | 90.1 | 8.9 | 1.0
| LWK | 72.0 | 25.2 | 2.8
| MEX | 69.0 | 25.9 | 5.2
| MKK | 73.4 | 25.3 | 1.3
| TSI | 95.1 | 4.9 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=21812969
|Title=Genome-Wide Association Study Identifies Candidate Genes for Parkinson's Disease in an Ashkenazi Jewish Population
|OA=1
}}

{{PMID Auto
|PMID=17903293
|Title=Genome-wide association with select biomarker traits in the Framingham Heart Study.
|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}}
{{on chip | Illumina Human 1M}}