{{Rsnum
|rsid=11176013
|Gene=LRRK2
|Chromosome=12
|position=40320071
|Orientation=plus
|GMAF=0.4642
|Gene_s=LRRK2
|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 | 17.7 | 43.4 | 38.9
| HCB | 29.4 | 52.2 | 18.4
| JPT | 31.9 | 46.9 | 21.2
| YRI | 18.4 | 49.0 | 32.7
| ASW | 17.5 | 61.4 | 21.1
| CHB | 29.4 | 52.2 | 18.4
| CHD | 24.8 | 51.4 | 23.9
| GIH | 13.0 | 41.0 | 46.0
| LWK | 22.0 | 47.7 | 30.3
| MEX | 8.6 | 58.6 | 32.8
| MKK | 14.7 | 57.7 | 27.6
| TSI | 18.8 | 54.5 | 26.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=23115130
|Title=Common variation in the LRRK2 gene is a risk factor for Parkinson's disease
|OA=1
}}

{{ClinVar
|ALT=G
|CAF=0.4642; 0.5358
|CHROM=12
|CLNACC=RCV000032473.1
|CLNALLE=1
|CLNDBN=Parkinson disease 8, autosomal dominant
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1208:NBK1223:C1846862:607060:2828
|CLNHGVS=NC_000012.11:g.40713873A>G
|CLNSRC=GeneReviews
|CLNSRCID=NBK1208
|COMMON=1
|Disease=Parkinson disease 8
|FwdALT=G
|FwdREF=A
|GENEINFO=LRRK2:120892
|GENE_ID=120892
|GENE_NAME=LRRK2
|REF=A
|RSPOS=40713873
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;VLD;G5A;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD
|VC=SNV
|VP=0x05016800000017051f100100
|WGT=0
|dbSNPBuildID=120
|rsid=11176013
}}

{{PMID Auto
|PMID=15726496
|Title=Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations.
|OA=1
}}

{{PMID Auto
|PMID=16960813
|Title=LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.
|OA=1
}}

{{PMID Auto
|PMID=18952485
|Title=Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism.
|OA=1
}}

{{PMID Auto
|PMID=19343804
|Title=LRRK2 mutations and risk variants in Japanese patients with Parkinson's 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}}