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

rs6799767

From SNPedia

Orientationplus
Stabilizedplus
Make rs6799767(G;G)
Make rs6799767(G;T)
Make rs6799767(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position176312308
is asnp
is mentioned by
dbSNPrs6799767
ebirs6799767
HLIrs6799767
Exacrs6799767
Varsomers6799767
Maprs6799767
PheGenIrs6799767
hapmaprs6799767
1000 genomesrs6799767
hgdprs6799767
ensemblrs6799767
gopubmedrs6799767
geneviewrs6799767
scholarrs6799767
googlers6799767
pharmgkbrs6799767
gwascentralrs6799767
openSNPrs6799767
23andMers6799767
23andMe allrs6799767
SNP Nexus

SNPshotrs6799767
SNPdbers6799767
MSV3drs6799767
GWAS Ctlgrs6799767
GMAF0.4839
Max Magnitude
? (G;G) (G;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
P-val 4E-7
Odds Ratio 1.49 [1.18-1.85]