{{Rsnum
|rsid=281865052
|Chromosome=12
|position=40323255
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=LRRK2
|Gene_s=LRRK2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=G
|CHROM=12
|CLNACC=RCV000032486.1
|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.40717057A>G
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1208
|Disease=Parkinson disease 8
|FwdALT=G
|FwdREF=A
|REF=A
|RSPOS=40717057
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=281865052
|GENEINFO=LRRK2:120892
|GENE_ID=120892
|GENE_NAME=LRRK2
}}{{PMID Auto
|PMID=16633828
|Title=A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan.
}}