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rs1491942

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1491942(C;C)
Make rs1491942(C;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position40227006
GeneLRRK2
is asnp
is mentioned by
dbSNPrs1491942
ebirs1491942
HLIrs1491942
Exacrs1491942
Varsomers1491942
Maprs1491942
PheGenIrs1491942
hapmaprs1491942
1000 genomesrs1491942
hgdprs1491942
ensemblrs1491942
gopubmedrs1491942
geneviewrs1491942
scholarrs1491942
googlers1491942
pharmgkbrs1491942
gwascentralrs1491942
openSNPrs1491942
23andMers1491942
23andMe allrs1491942
SNP Nexus

SNPshotrs1491942
SNPdbers1491942
MSV3drs1491942
GWAS Ctlgrs1491942
GMAF0.2741
Max Magnitude0
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 21292315OA-icon.png]
Trait
Title Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
Risk Allele G
P-val 6E-14
Odds Ratio 1.2700 [1.21-1.33]
GWAS snp
PMID [PMID 22438815OA-icon.png]
Trait
Title Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
Risk Allele
P-val 6E-15
Odds Ratio 1.1700 None