{{Rsnum
|rsid=74163686
|Chromosome=12
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=LRRK2
|Gene_s=LRRK2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|position=40309225
}}{{ClinVar
|ALT=C
|CHROM=12
|CLNACC=RCV000032457.1
|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.40703027A>C
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1208
|Disease=Parkinson disease 8
|FwdALT=C
|FwdREF=A
|GENEINFO=LRRK2:120892
|GENE_ID=120892
|GENE_NAME=LRRK2
|REF=A
|RSPOS=40703027
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=130
|rsid=74163686
}}{{PMID Auto
|PMID=21641848
|Title=Subclinical signs in LRRK2 mutation carriers.
}}