{{Rsnum
|rsid=35808389
|Chromosome=12
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=LRRK2
|Gene_s=LRRK2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|position=40298488
}}{{ClinVar
|ALT=G
|CHROM=12
|CLNACC=RCV000032438.1
|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.40692290A>G
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1208
|Disease=Parkinson disease 8
|FwdALT=G
|FwdREF=A
|GENEINFO=LRRK2:120892
|GENE_ID=120892
|GENE_NAME=LRRK2
|REF=A
|RSPOS=40692290
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;HD;GNO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000502110100
|WGT=0
|dbSNPBuildID=126
|rsid=35808389
}}

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

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