{{Rsnum
|rsid=356220
|Chromosome=4
|position=89720189
|Orientation=plus
|GMAF=0.4219
|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 | 34.5 | 50.4 | 15.0
| HCB | 24.1 | 51.9 | 24.1
| JPT | 16.1 | 48.2 | 35.7
| YRI | 3.4 | 37.9 | 58.6
| ASW | 10.5 | 42.1 | 47.4
| CHB | 24.1 | 51.9 | 24.1
| CHD | 15.7 | 55.6 | 28.7
| GIH | 32.0 | 56.0 | 12.0
| LWK | 7.4 | 40.7 | 51.9
| MEX | 13.8 | 60.3 | 25.9
| MKK | 5.2 | 43.9 | 51.0
| TSI | 37.6 | 43.6 | 18.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20711177
|Trait=None
|Title=Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease
|RiskAllele=T
|Pval=3E-11
|OR=1.38
|ORtxt=[1.25-1.52]
|OA=1
}}

{{PMID Auto GWAS
|PMID=21084426
|Trait=None
|Title=Genome-wide association study confirms BST1 and suggests a locus on 12q24 as risk loci for Parkinson's disease in the European population
|RiskAllele=T
|Pval=3E-8
|OR=1.3700
|ORtxt=[NR]
}}
{{PMID Auto GWAS
|PMID=21044948
|Trait=None
|Title=Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21
|RiskAllele=A
|Pval=9E-16
|OR=1.2700
|ORtxt=[1.17-1.37]
|OA=1
}}

{{PMID Auto GWAS
|PMID=21738487
|Trait=None
|Title=Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease.
|RiskAllele=T
|Pval=2E-19
|OR=1.2900
|ORtxt=[1.22-1.36]
|OA=1
}}

{{PMID Auto GWAS
|PMID=22451204
|Trait=None
|Title=Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.
|RiskAllele=
|Pval=8E-35
|OR=1.3800
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=22839974
|Title=UCHL1 S18Y variant is a risk factor for Parkinson's disease in Japan
|OA=1
}}

{{PMID Auto
|PMID=15637659
|Title=Linkage disequilibrium patterns and tagSNP transferability among European populations.
|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=20070850
|Title=Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}