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rs11154851

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common genotype
Make rs11154851(C;T)
Make rs11154851(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position136046867
GeneLOC644135, PDE7B
is asnp
is mentioned by
dbSNPrs11154851
dbSNP (classic)rs11154851
ClinGenrs11154851
ebirs11154851
HLIrs11154851
Exacrs11154851
Gnomadrs11154851
Varsomers11154851
LitVarrs11154851
Maprs11154851
PheGenIrs11154851
Biobankrs11154851
1000 genomesrs11154851
hgdprs11154851
ensemblrs11154851
geneviewrs11154851
scholarrs11154851
googlers11154851
pharmgkbrs11154851
gwascentralrs11154851
openSNPrs11154851
23andMers11154851
SNPshotrs11154851
SNPdbers11154851
MSV3drs11154851
GWAS Ctlgrs11154851
GMAF0.07851
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23535033OA-icon.png]
Trait Alzheimer's disease (cognitive decline)
Title Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.
Risk Allele
P-val 1E-8
Odds Ratio .25 unit decrease