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rs10889676

From SNPedia

Orientationplus
Stabilizedplus
Make rs10889676(A;A)
Make rs10889676(A;C)
Make rs10889676(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position67256884
GeneIL23R
is asnp
is mentioned by
dbSNPrs10889676
ebirs10889676
HLIrs10889676
Exacrs10889676
Varsomers10889676
Maprs10889676
PheGenIrs10889676
hapmaprs10889676
1000 genomesrs10889676
hgdprs10889676
ensemblrs10889676
gopubmedrs10889676
geneviewrs10889676
scholarrs10889676
googlers10889676
pharmgkbrs10889676
gwascentralrs10889676
openSNPrs10889676
23andMers10889676
23andMe allrs10889676
SNP Nexus

SNPshotrs10889676
SNPdbers10889676
MSV3drs10889676
GWAS Ctlgrs10889676
GMAF0.365
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS
SNP rs10889676
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
rs10889676
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.328125
summary