{{Rsnum
|rsid=11737074
|Chromosome=4
|position=124160218
|Orientation=plus
|GMAF=0.14
|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 | 4.6 | 36.9 | 58.5
| HCB | 6.7 | 13.3 | 80.0
| JPT | 2.3 | 15.9 | 81.8
| YRI | 1.6 | 19.0 | 79.4
| ASW | 0.0 | 0.0 | 0.0
| CHB | 6.7 | 13.3 | 80.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

rs11737074 increases susceptibility to Parkinson's disease 1.50 times for carriers of the A allele {{PMID|16252231|OA=1
}}

{{PMID Auto
|PMID=16685661
|Title=Genomewide association, Parkinson disease, and PARK10.
|OA=1
}}

{{PMID Auto
|PMID=16685662
|Title=No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.
|OA=1
}}

{{PMID Auto
|PMID=16685663
|Title=A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}