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rs4746003

From SNPedia

Orientationplus
Stabilizedplus
Make rs4746003(C;C)
Make rs4746003(C;T)
Make rs4746003(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position69778536
GeneRPL5P26
is asnp
is mentioned by
dbSNPrs4746003
ClinGenrs4746003
ebirs4746003
HLIrs4746003
Exacrs4746003
Varsomers4746003
Maprs4746003
PheGenIrs4746003
hapmaprs4746003
1000 genomesrs4746003
hgdprs4746003
ensemblrs4746003
gopubmedrs4746003
geneviewrs4746003
scholarrs4746003
googlers4746003
pharmgkbrs4746003
gwascentralrs4746003
openSNPrs4746003
23andMers4746003
23andMe allrs4746003
SNP Nexus

SNPshotrs4746003
SNPdbers4746003
MSV3drs4746003
GWAS Ctlgrs4746003
GMAF0.2475
Max Magnitude
? (C;C) (C;T) (T;T) 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 0.000006
Odds Ratio 1.3000 None