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rs3806932

From SNPedia

Orientationplus
Stabilizedplus
Make rs3806932(A;A)
Make rs3806932(A;G)
Make rs3806932(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position111069977
GeneTSLP
is asnp
is mentioned by
dbSNPrs3806932
ebirs3806932
HLIrs3806932
Exacrs3806932
Varsomers3806932
Maprs3806932
PheGenIrs3806932
hapmaprs3806932
1000 genomesrs3806932
hgdprs3806932
ensemblrs3806932
gopubmedrs3806932
geneviewrs3806932
scholarrs3806932
googlers3806932
pharmgkbrs3806932
gwascentralrs3806932
openSNPrs3806932
23andMers3806932
23andMe allrs3806932
SNP Nexus

SNPshotrs3806932
SNPdbers3806932
MSV3drs3806932
GWAS Ctlgrs3806932
GMAF0.4692
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 3E-9
Odds Ratio 1.85 None
OMIM613412
Desc
Variant
Relatedalso