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rs9811423

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;G) 0 common in complete genomics
Make rs9811423(C;C)
Make rs9811423(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position113103475
is asnp
is mentioned by
dbSNPrs9811423
ebirs9811423
HLIrs9811423
Exacrs9811423
Varsomers9811423
Maprs9811423
PheGenIrs9811423
hapmaprs9811423
1000 genomesrs9811423
hgdprs9811423
ensemblrs9811423
gopubmedrs9811423
geneviewrs9811423
scholarrs9811423
googlers9811423
pharmgkbrs9811423
gwascentralrs9811423
openSNPrs9811423
23andMers9811423
23andMe allrs9811423
SNP Nexus

SNPshotrs9811423
SNPdbers9811423
MSV3drs9811423
GWAS Ctlgrs9811423
GMAF0.2837
Max Magnitude0
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 22005930OA-icon.png]
Trait
Title Genome-wide association study of Alzheimer's disease with psychotic symptoms.
Risk Allele
P-val 0.000004
Odds Ratio 1.2800 None