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rs35801418

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs35801418(A;G)
Make rs35801418(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position40321114
GeneLRRK2
is asnp
is mentioned by
dbSNPrs35801418
ebirs35801418
HLIrs35801418
Exacrs35801418
Varsomers35801418
Maprs35801418
PheGenIrs35801418
hapmaprs35801418
1000 genomesrs35801418
hgdprs35801418
ensemblrs35801418
gopubmedrs35801418
geneviewrs35801418
scholarrs35801418
googlers35801418
pharmgkbrs35801418
gwascentralrs35801418
openSNPrs35801418
23andMers35801418
23andMe allrs35801418
SNP Nexus

SNPshotrs35801418
SNPdbers35801418
MSV3drs35801418
GWAS Ctlgrs35801418
Max Magnitude0
OMIM609007
Desc
Variant0002
Relatedalso


ClinVar
Risk rs35801418(G;G)
Alt rs35801418(G;G)
Reference rs35801418(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.40714916A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000002014.2,



[PMID 15541308] Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease.


[PMID 15541309] Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.