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rs9500256

From SNPedia

Orientationplus
Stabilizedplus
Make rs9500256(A;A)
Make rs9500256(A;G)
Make rs9500256(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position57982677
is asnp
is mentioned by
dbSNPrs9500256
ebirs9500256
HLIrs9500256
Exacrs9500256
Varsomers9500256
Maprs9500256
PheGenIrs9500256
hapmaprs9500256
1000 genomesrs9500256
hgdprs9500256
ensemblrs9500256
gopubmedrs9500256
geneviewrs9500256
scholarrs9500256
googlers9500256
pharmgkbrs9500256
gwascentralrs9500256
openSNPrs9500256
23andMers9500256
23andMe allrs9500256
SNP Nexus

SNPshotrs9500256
SNPdbers9500256
MSV3drs9500256
GWAS Ctlgrs9500256
GMAF0.4803
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 0.000005
Odds Ratio 2.04 [1.52-2.70]