{{Rsnum
|rsid=356229
|Chromosome=4
|position=89685446
|Orientation=minus
|GMAF=0.259
|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 | 35.4 | 47.8 | 16.8
| HCB | 97.1 | 2.9 | 0.0
| JPT | 92.0 | 8.0 | 0.0
| YRI | 41.5 | 49.0 | 9.5
| ASW | 45.6 | 49.1 | 5.3
| CHB | 97.1 | 2.9 | 0.0
| CHD | 99.1 | 0.9 | 0.0
| GIH | 66.3 | 30.7 | 3.0
| LWK | 41.8 | 44.5 | 13.6
| MEX | 56.9 | 36.2 | 6.9
| MKK | 32.7 | 48.1 | 19.2
| TSI | 35.3 | 45.1 | 19.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=21058943
|Title=Replication of GWAS associations for GAK and MAPT in Parkinson's disease
|OA=1
}}

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

{{PMID Auto
|PMID=18985386
|Title=Genomewide association study for susceptibility genes contributing to familial Parkinson disease.
|OA=1
}}

{{PMID Auto
|PMID=19771175
|Title=Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy.
|OA=1
}}

{{PMID Auto
|PMID=22425546
|Title=SNCA polymorphisms, smoking, and sporadic Parkinson's disease in Japanese.
}}

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