{{Rsnum
|rsid=33939927
|Chromosome=12
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=LRRK2
|position=40310434
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LRRK2
}}{{omim
|id=609007
|rsnum=33939927
|variant=0001
}}
{{omim
|id=609007
|rsnum=33939927
|variant=0003
}}

{{ClinVar
|rsid=33939927
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=40704236
|CHROM=12
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000502110100
|GENEINFO=LRRK2:120892
|GENE_NAME=LRRK2
|GENE_ID=120892
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000012.11:g.40704236C>G; NC_000012.11:g.40704236C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1208; 609007.0001; 609007.0003
|CLNSIG=5
|CLNCUI=CN068515
|CLNDBN=Parkinson disease 8, autosomal dominant
|Disease=Parkinson disease 8
|CLNACC=RCV000002013.1; RCV000002015.1
|Tags=PM;PMC;S3D;SLO;HD;GNO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1208:NBK1223:C1846862:607060:2828
}}

{{PMID Auto
|PMID=15541309
|Title=Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.
}}

{{PMID Auto
|PMID=15541308
|Title=Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}