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rs7236477

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common on affy axiom data
Make rs7236477(A;G)
Make rs7236477(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position31322359
GeneDSG1
is asnp
is mentioned by
dbSNPrs7236477
ebirs7236477
HLIrs7236477
Exacrs7236477
Varsomers7236477
Maprs7236477
PheGenIrs7236477
hapmaprs7236477
1000 genomesrs7236477
hgdprs7236477
ensemblrs7236477
gopubmedrs7236477
geneviewrs7236477
scholarrs7236477
googlers7236477
pharmgkbrs7236477
gwascentralrs7236477
openSNPrs7236477
23andMers7236477
23andMe allrs7236477
SNP Nexus

SNPshotrs7236477
SNPdbers7236477
MSV3drs7236477
GWAS Ctlgrs7236477
GMAF0.06382
Max Magnitude0
? (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 G
P-val 0.000007
Odds Ratio 2.22 [1.39-3.55]