{{Rsnum
|rsid=78365431
|Gene=LRRK2
|Chromosome=12
|position=40298479
|Orientation=plus
|GMAF=0.002755
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=LRRK2
}}{{PMID Auto
|PMID=21632271
|Title=Lrrk2 p.Q1111H substitution and Parkinson's disease in Latin America
|OA=1
}}{{ClinVar
|ALT=T
|CAF=0.9972; 0.002755
|CHROM=12
|CLNACC=RCV000032437.1
|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.40692281G>T
|CLNSRC=GeneReviews
|CLNSRCID=NBK1208
|COMMON=1
|Disease=Parkinson disease 8
|FwdALT=T
|FwdREF=G
|GENEINFO=LRRK2:120892
|GENE_ID=120892
|GENE_NAME=LRRK2
|REF=G
|RSPOS=40692281
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;SLO;KGPhase1;KGPROD;OTHERKG;LSD
|VC=SNV
|VP=0x050160000000000016100100
|WGT=0
|dbSNPBuildID=131
|rsid=78365431
}}