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rs2224865

From SNPedia

Orientationplus
Stabilizedplus
Make rs2224865(G;G)
Make rs2224865(G;T)
Make rs2224865(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position83663098
is asnp
is mentioned by
dbSNPrs2224865
ebirs2224865
HLIrs2224865
Exacrs2224865
Varsomers2224865
Maprs2224865
PheGenIrs2224865
hapmaprs2224865
1000 genomesrs2224865
hgdprs2224865
ensemblrs2224865
gopubmedrs2224865
geneviewrs2224865
scholarrs2224865
googlers2224865
pharmgkbrs2224865
gwascentralrs2224865
openSNPrs2224865
23andMers2224865
23andMe allrs2224865
SNP Nexus

SNPshotrs2224865
SNPdbers2224865
MSV3drs2224865
GWAS Ctlgrs2224865
GMAF0.3531
Max Magnitude
? (G;G) (G;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 G
P-val 0.000009
Odds Ratio 1.44 [1.15-1.79]