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rs11889338

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs11889338(A;A)
Make rs11889338(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position17246318
is asnp
is mentioned by
dbSNPrs11889338
ebirs11889338
HLIrs11889338
Exacrs11889338
Varsomers11889338
Maprs11889338
PheGenIrs11889338
hapmaprs11889338
1000 genomesrs11889338
hgdprs11889338
ensemblrs11889338
gopubmedrs11889338
geneviewrs11889338
scholarrs11889338
googlers11889338
pharmgkbrs11889338
gwascentralrs11889338
openSNPrs11889338
23andMers11889338
23andMe allrs11889338
SNP Nexus

SNPshotrs11889338
SNPdbers11889338
MSV3drs11889338
GWAS Ctlgrs11889338
GMAF0.1152
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22159054OA-icon.png]
Trait
Title A comprehensive genetic association study of Alzheimer disease in African Americans.
Risk Allele A
P-val 0.000009
Odds Ratio 1.5500 None