{{Rsnum
|rsid=1223271
|Chromosome=20
|position=13316265
|Orientation=plus
|GMAF=0.1892
|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 | 2.7 | 17.0 | 80.4
| HCB | 20.6 | 48.5 | 30.9
| JPT | 12.4 | 48.7 | 38.9
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 5.3 | 94.7
| CHB | 20.6 | 48.5 | 30.9
| CHD | 19.3 | 41.3 | 39.4
| GIH | 7.9 | 41.6 | 50.5
| LWK | 0.0 | 2.7 | 97.3
| MEX | 8.6 | 27.6 | 63.8
| MKK | 0.0 | 7.2 | 92.8
| TSI | 2.0 | 29.4 | 68.6
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19915575
|Trait=Parkinson's disease
|Title=Genome-wide association study reveals genetic risk underlying Parkinson's disease
|RiskAllele=A
|Pval=0.000005
|OR=1.18
|ORtxt=[NR]
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1223271
|overall_frequency_n=17
|overall_frequency_d=128
|overall_frequency=0.132812
|n_genomes=10
|n_genomes_annotated=0
|n_haplomes=11
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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