Have questions? Visit https://www.reddit.com/r/SNPedia

rs6501384

From SNPedia

Orientationplus
Stabilizedplus
Make rs6501384(C;C)
Make rs6501384(C;T)
Make rs6501384(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position70294992
is asnp
is mentioned by
dbSNPrs6501384
ebirs6501384
HLIrs6501384
Exacrs6501384
Varsomers6501384
Maprs6501384
PheGenIrs6501384
hapmaprs6501384
1000 genomesrs6501384
hgdprs6501384
ensemblrs6501384
gopubmedrs6501384
geneviewrs6501384
scholarrs6501384
googlers6501384
pharmgkbrs6501384
gwascentralrs6501384
openSNPrs6501384
23andMers6501384
23andMe allrs6501384
SNP Nexus

SNPshotrs6501384
SNPdbers6501384
MSV3drs6501384
GWAS Ctlgrs6501384
GMAF0.2934
Max Magnitude
? (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 0.000006
Odds Ratio 1.41 [1.13-1.76]