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rs34410987

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs34410987(C;T)
Make rs34410987(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position40283897
GeneLRRK2
is asnp
is mentioned by
dbSNPrs34410987
ebirs34410987
HLIrs34410987
Exacrs34410987
Varsomers34410987
Maprs34410987
PheGenIrs34410987
hapmaprs34410987
1000 genomesrs34410987
hgdprs34410987
ensemblrs34410987
gopubmedrs34410987
geneviewrs34410987
scholarrs34410987
googlers34410987
pharmgkbrs34410987
gwascentralrs34410987
openSNPrs34410987
23andMers34410987
23andMe allrs34410987
SNP Nexus

SNPshotrs34410987
SNPdbers34410987
MSV3drs34410987
GWAS Ctlgrs34410987
GMAF0.001837
Max Magnitude0
ClinVar
Risk rs34410987(T;T)
Alt rs34410987(T;T)
Reference rs34410987(C;C)
Significance Pathogenic
Disease Parkinson disease 8
Variation info
Gene LRRK2
CLNDBN Parkinson disease 8, autosomal dominant
Reversed 0
HGVS NC_000012.11:g.40677699C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000032422.1,



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