{{Rsnum
|rsid=1491923
|Chromosome=12
|position=40197315
|Orientation=plus
|GMAF=0.3682
|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 | 13.3 | 33.6 | 53.1
| HCB | 19.1 | 43.4 | 37.5
| JPT | 12.5 | 50.9 | 36.6
| YRI | 13.7 | 46.6 | 39.7
| ASW | 7.1 | 48.2 | 44.6
| CHB | 19.1 | 43.4 | 37.5
| CHD | 12.0 | 45.4 | 42.6
| GIH | 14.9 | 46.5 | 38.6
| LWK | 14.5 | 50.9 | 34.5
| MEX | 28.6 | 51.8 | 19.6
| MKK | 4.5 | 42.9 | 52.6
| TSI | 8.8 | 46.1 | 45.1
| HapMapRevision=28
}}{{omim
|desc=LEUCINE-RICH REPEAT KINASE 2; LRRK2
|id=609007
|rsnum=1491923
}}

{{omim
|id=613164
|rsnum=1491923
}}

{{PMID Auto
|PMID=19915575
|Title=Genome-wide association study reveals genetic risk underlying Parkinson's disease.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}