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rs281865052

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281865052(A;G)
Make rs281865052(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position40323255
GeneLRRK2
is asnp
is mentioned by
dbSNPrs281865052
ebirs281865052
HLIrs281865052
Exacrs281865052
Varsomers281865052
Maprs281865052
PheGenIrs281865052
hapmaprs281865052
1000 genomesrs281865052
hgdprs281865052
ensemblrs281865052
gopubmedrs281865052
geneviewrs281865052
scholarrs281865052
googlers281865052
pharmgkbrs281865052
gwascentralrs281865052
openSNPrs281865052
23andMers281865052
23andMe allrs281865052
SNP Nexus

SNPshotrs281865052
SNPdbers281865052
MSV3drs281865052
GWAS Ctlgrs281865052
Max Magnitude0
ClinVar
Risk rs281865052(G;G)
Alt rs281865052(G;G)
Reference rs281865052(A;A)
Significance Pathogenic
Disease Parkinson disease 8
Variation info
Gene LRRK2
CLNDBN Parkinson disease 8, autosomal dominant
Reversed 0
HGVS NC_000012.11:g.40717057A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000032486.1,


[PMID 16633828] A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan.