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rs13106227

From SNPedia

Orientationplus
Stabilizedplus
Make rs13106227(A;A)
Make rs13106227(A;G)
Make rs13106227(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position76497528
GeneSHROOM3
is asnp
is mentioned by
dbSNPrs13106227
ebirs13106227
HLIrs13106227
Exacrs13106227
Varsomers13106227
Maprs13106227
PheGenIrs13106227
hapmaprs13106227
1000 genomesrs13106227
hgdprs13106227
ensemblrs13106227
gopubmedrs13106227
geneviewrs13106227
scholarrs13106227
googlers13106227
pharmgkbrs13106227
gwascentralrs13106227
openSNPrs13106227
23andMers13106227
23andMe allrs13106227
SNP Nexus

SNPshotrs13106227
SNPdbers13106227
MSV3drs13106227
GWAS Ctlgrs13106227
GMAF0.4477
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 0.000004
Odds Ratio 1.52 [1.20-1.92]