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rs2064689

From SNPedia

Orientationplus
Stabilizedplus
Make rs2064689(A;A)
Make rs2064689(A;G)
Make rs2064689(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position67187327
GeneIL23R
is asnp
is mentioned by
dbSNPrs2064689
ebirs2064689
HLIrs2064689
Exacrs2064689
Varsomers2064689
Maprs2064689
PheGenIrs2064689
hapmaprs2064689
1000 genomesrs2064689
hgdprs2064689
ensemblrs2064689
gopubmedrs2064689
geneviewrs2064689
scholarrs2064689
googlers2064689
pharmgkbrs2064689
gwascentralrs2064689
openSNPrs2064689
23andMers2064689
23andMe allrs2064689
SNP Nexus

SNPshotrs2064689
SNPdbers2064689
MSV3drs2064689
GWAS Ctlgrs2064689
GMAF0.3081
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs2064689
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



[PMID 17068223OA-icon.png] A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.


[PMID 20369022OA-icon.png] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.


[PMID 21304977OA-icon.png] An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians.


GET Evidence
rs2064689
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.3125
summary