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rs13178362

From SNPedia

Orientationplus
Stabilizedplus
Make rs13178362(C;C)
Make rs13178362(C;T)
Make rs13178362(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position30178906
is asnp
is mentioned by
dbSNPrs13178362
dbSNP (classic)rs13178362
ClinGenrs13178362
ebirs13178362
HLIrs13178362
Exacrs13178362
Gnomadrs13178362
Varsomers13178362
LitVarrs13178362
Maprs13178362
PheGenIrs13178362
Biobankrs13178362
1000 genomesrs13178362
hgdprs13178362
ensemblrs13178362
geneviewrs13178362
scholarrs13178362
googlers13178362
pharmgkbrs13178362
gwascentralrs13178362
openSNPrs13178362
23andMers13178362
SNPshotrs13178362
SNPdbers13178362
MSV3drs13178362
GWAS Ctlgrs13178362
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 24755620OA-icon.png]
Trait Alzheimer's disease
Title Overrepresentation of glutamate signaling in Alzheimer's disease: network-based pathway enrichment using meta-analysis of genome-wide association studies.
Risk Allele T
P-val 7E-7
Odds Ratio 1.33 [NR]