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rs371915

From SNPedia

Orientationplus
Stabilizedplus
Make rs371915(A;A)
Make rs371915(A;G)
Make rs371915(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position84544635
is asnp
is mentioned by
dbSNPrs371915
ebirs371915
HLIrs371915
Exacrs371915
Varsomers371915
Maprs371915
PheGenIrs371915
hapmaprs371915
1000 genomesrs371915
hgdprs371915
ensemblrs371915
gopubmedrs371915
geneviewrs371915
scholarrs371915
googlers371915
pharmgkbrs371915
gwascentralrs371915
openSNPrs371915
23andMers371915
23andMe allrs371915
SNP Nexus

SNPshotrs371915
SNPdbers371915
MSV3drs371915
GWAS Ctlgrs371915
GMAF0.1405
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20208534OA-icon.png]
Trait Eosinophilic esophagitis (pediatric)
Title Common variants at 5q22 associate with pediatric eosinophilic esophagitis
Risk Allele
P-val 2E-8
Odds Ratio 1.90 [1.44-2.50]