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rs6669582

From SNPedia

Orientationplus
Stabilizedplus
Make rs6669582(A;A)
Make rs6669582(A;G)
Make rs6669582(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position67264372
is asnp
is mentioned by
dbSNPrs6669582
dbSNP (classic)rs6669582
ClinGenrs6669582
ebirs6669582
HLIrs6669582
Exacrs6669582
Gnomadrs6669582
Varsomers6669582
LitVarrs6669582
Maprs6669582
PheGenIrs6669582
Biobankrs6669582
1000 genomesrs6669582
hgdprs6669582
ensemblrs6669582
geneviewrs6669582
scholarrs6669582
googlers6669582
pharmgkbrs6669582
gwascentralrs6669582
openSNPrs6669582
23andMers6669582
SNPshotrs6669582
SNPdbers6669582
MSV3drs6669582
GWAS Ctlgrs6669582
GMAF0.2805
Max Magnitude0
GWAS
SNP rs6669582
PubMedID [PMID 17804789OA-icon.png]
Condition Crohn's disease
Gene IL23R
Risk Allele
pValue 1.00E-008
OR 1.38
95% CI 1.23-1.53