{{Rsnum
|rsid=11012
|Gene=PLEKHM1
|Chromosome=17
|position=45436075
|Orientation=minus
|GMAF=0.1065
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PLEKHM1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.9 | 31.0 | 68.1
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.9 | 99.1
| YRI | 0.0 | 6.1 | 93.9
| ASW | 0.0 | 15.8 | 84.2
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 12.9 | 87.1
| LWK | 0.0 | 12.7 | 87.3
| MEX | 6.9 | 22.4 | 70.7
| MKK | 2.6 | 10.9 | 86.5
| TSI | 12.7 | 37.3 | 50.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20070850
|Trait=Parkinson's disease
|Title=Genome-Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease
|RiskAllele=T
|Pval=6E-8
|OR=1.43
|ORtxt=[1.27-1.61]
|OA=1
}}

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

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