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rs1032757

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1032757(C;T)
Make rs1032757(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position82643499
is asnp
is mentioned by
dbSNPrs1032757
ebirs1032757
HLIrs1032757
Exacrs1032757
Varsomers1032757
Maprs1032757
PheGenIrs1032757
hapmaprs1032757
1000 genomesrs1032757
hgdprs1032757
ensemblrs1032757
gopubmedrs1032757
geneviewrs1032757
scholarrs1032757
googlers1032757
pharmgkbrs1032757
gwascentralrs1032757
openSNPrs1032757
23andMers1032757
23andMe allrs1032757
SNP Nexus

SNPshotrs1032757
SNPdbers1032757
MSV3drs1032757
GWAS Ctlgrs1032757
GMAF0.1887
Max Magnitude0
? (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 0.000002
Odds Ratio 1.96 [1.40-2.74]