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rs11989782

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;C) 0 common in complete genomics
Make rs11989782(A;A)
Make rs11989782(C;C)
ReferenceGRCh38 38.1/141
Chromosome8
Position120682410
GeneSNTB1
is asnp
is mentioned by
dbSNPrs11989782
ebirs11989782
HLIrs11989782
Exacrs11989782
Varsomers11989782
Maprs11989782
PheGenIrs11989782
hapmaprs11989782
1000 genomesrs11989782
hgdprs11989782
ensemblrs11989782
gopubmedrs11989782
geneviewrs11989782
scholarrs11989782
googlers11989782
pharmgkbrs11989782
gwascentralrs11989782
openSNPrs11989782
23andMers11989782
23andMe allrs11989782
SNP Nexus

SNPshotrs11989782
SNPdbers11989782
MSV3drs11989782
GWAS Ctlgrs11989782
GMAF0.14
Max Magnitude0
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 20208534OA-icon.png]
Trait Eosinophilic esophagitis (pediatric)
Title Common variants at 5q22 associate with pediatric eosinophilic esophagitis
Risk Allele A
P-val 0.000007
Odds Ratio 1.53 [1.21-1.93]