{{Rsnum
|rsid=34410987
|Gene=LRRK2
|Chromosome=12
|position=40283897
|Orientation=plus
|GMAF=0.001837
|Gene_s=LRRK2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ClinVar
|ALT=T
|CAF=0.9982; 0.001837
|CHROM=12
|CLNACC=RCV000032422.1
|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.40677699C>T
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1208
|COMMON=1
|Disease=Parkinson disease 8
|FwdALT=T
|FwdREF=C
|GENEINFO=LRRK2:120892
|GENE_ID=120892
|GENE_NAME=LRRK2
|REF=C
|RSPOS=40677699
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;VLD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000040116110100
|WGT=0
|dbSNPBuildID=126
|rsid=34410987
}}

{{PMID Auto
|PMID=16633828
|Title=A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan.
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}