{{Rsnum
|rsid=2301134
|Gene=SNCA
|Chromosome=4
|position=89837794
|Orientation=minus
|GMAF=0.3485
|Gene_s=FGF22,SNCA
|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 | 25.2 | 53.2 | 21.6
| HCB | 75.9 | 19.7 | 4.4
| JPT | 85.0 | 15.0 | 0.0
| YRI | 54.8 | 37.7 | 7.5
| ASW | 50.9 | 36.8 | 12.3
| CHB | 75.9 | 19.7 | 4.4
| CHD | 79.8 | 18.3 | 1.8
| GIH | 24.8 | 53.5 | 21.8
| LWK | 42.7 | 50.0 | 7.3
| MEX | 32.8 | 50.0 | 17.2
| MKK | 58.3 | 32.7 | 9.0
| TSI | 23.5 | 48.0 | 28.4
| HapMapRevision=28
}}{{PMID Auto
|PMID=23182315
|Title=Genetic variants of SNCA and LRRK2 genes are associated with sporadic PD susceptibility: A replication study in a Taiwanese cohort
}}

{{PMID Auto
|PMID=15637659
|Title=Linkage disequilibrium patterns and tagSNP transferability among European populations.
|OA=1
}}

{{PMID Auto
|PMID=19063963
|Title=Genetic susceptibility in Parkinson's disease.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}