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rs11012

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs11012(A;A)
Make rs11012(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position45436075
GenePLEKHM1
is asnp
is mentioned by
dbSNPrs11012
ebirs11012
HLIrs11012
Exacrs11012
Varsomers11012
Maprs11012
PheGenIrs11012
hapmaprs11012
1000 genomesrs11012
hgdprs11012
ensemblrs11012
gopubmedrs11012
geneviewrs11012
scholarrs11012
googlers11012
pharmgkbrs11012
gwascentralrs11012
openSNPrs11012
23andMers11012
23andMe allrs11012
SNP Nexus

SNPshotrs11012
SNPdbers11012
MSV3drs11012
GWAS Ctlgrs11012
GMAF0.1065
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20070850OA-icon.png]
Trait Parkinson's disease
Title Genome-Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease
Risk Allele T
P-val 6E-8
Odds Ratio 1.43 [1.27-1.61]


[PMID 18985386OA-icon.png] Genomewide association study for susceptibility genes contributing to familial Parkinson disease.