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rs13278732

From SNPedia

Orientationplus
Stabilizedplus
Make rs13278732(C;C)
Make rs13278732(C;T)
Make rs13278732(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position98076353
GeneERICH5
is asnp
is mentioned by
dbSNPrs13278732
ebirs13278732
HLIrs13278732
Exacrs13278732
Varsomers13278732
Maprs13278732
PheGenIrs13278732
hapmaprs13278732
1000 genomesrs13278732
hgdprs13278732
ensemblrs13278732
gopubmedrs13278732
geneviewrs13278732
scholarrs13278732
googlers13278732
pharmgkbrs13278732
gwascentralrs13278732
openSNPrs13278732
23andMers13278732
23andMe allrs13278732
SNP Nexus

SNPshotrs13278732
SNPdbers13278732
MSV3drs13278732
GWAS Ctlgrs13278732
GMAF0.1722
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20208534OA-icon.png]
Trait Eosinophilic esophagitis (pediatric)
Title Common variants at 5q22 associate with pediatric eosinophilic esophagitis
Risk Allele T
P-val 0.000006
Odds Ratio 1.31 [1.04-1.65]