{{Rsnum
|rsid=6532197
|Chromosome=4
|position=89876150
|Orientation=plus
|GMAF=0.2029
|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 | 84.1 | 15.0 | 0.9
| HCB | 53.7 | 39.7 | 6.6
| JPT | 47.8 | 42.5 | 9.7
| YRI | 37.4 | 51.7 | 10.9
| ASW | 43.9 | 43.9 | 12.3
| CHB | 53.7 | 39.7 | 6.6
| CHD | 40.2 | 53.3 | 6.5
| GIH | 86.1 | 12.9 | 1.0
| LWK | 44.0 | 43.1 | 12.8
| MEX | 87.9 | 8.6 | 3.4
| MKK | 37.2 | 48.7 | 14.1
| TSI | 81.4 | 17.6 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19915575
|Trait=Parkinson's disease
|Title=Genome-wide association study reveals genetic risk underlying Parkinson's disease
|RiskAllele=G
|Pval=1E-7
|OR=1.32
|ORtxt=[NR]
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6532197
|overall_frequency_n=29
|overall_frequency_d=128
|overall_frequency=0.226562
|n_genomes=20
|n_genomes_annotated=0
|n_haplomes=26
|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}}