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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
ebirs6669582
HLIrs6669582
Exacrs6669582
Varsomers6669582
Maprs6669582
PheGenIrs6669582
hapmaprs6669582
1000 genomesrs6669582
hgdprs6669582
ensemblrs6669582
gopubmedrs6669582
geneviewrs6669582
scholarrs6669582
googlers6669582
pharmgkbrs6669582
gwascentralrs6669582
openSNPrs6669582
23andMers6669582
23andMe allrs6669582
SNP Nexus

SNPshotrs6669582
SNPdbers6669582
MSV3drs6669582
GWAS Ctlgrs6669582
GMAF0.2805
Max Magnitude
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



GET Evidence
rs6669582
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.34375
summary