{{Rsnum
|rsid=10889676
|Gene=IL23R
|Chromosome=1
|position=67256884
|Orientation=plus
|GMAF=0.365
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=IL23R
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 9.7 | 38.9 | 51.3
| HCB | 51.8 | 40.1 | 8.0
| JPT | 48.7 | 38.1 | 13.3
| YRI | 1.4 | 21.8 | 76.9
| ASW | 0.0 | 29.8 | 70.2
| CHB | 51.8 | 40.1 | 8.0
| CHD | 51.4 | 44.0 | 4.6
| GIH | 37.6 | 45.5 | 16.8
| LWK | 5.5 | 28.2 | 66.4
| MEX | 10.3 | 34.5 | 55.2
| MKK | 9.0 | 44.2 | 46.8
| TSI | 5.9 | 52.0 | 42.2
| HapMapRevision=28
}}

{{GWAS Summary
|SNP=rs10889676
|PubMedID=17804789
|Condition=Crohn's disease
|Gene=IL23R
|Risk Allele=
|pValue=1.00E-008
|OR=1.38
|95CI=1.23-1.53
|OA=1
}}

{{PharmGKB
|RSID=rs10889676
|Name_s=
|Gene_s=IL23R
|Feature=
|Evidence=PubMed ID:17804789; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci (Initial Sample Size: 382 trios; Replication Sample Size: 521 trios, 750 cases, 828 controls). This variant is associated with Crohn's disease. This variant is associated with Crohn's disease.
|Drugs=
|Drug Classes=
|Diseases=Crohn Disease
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA162356495
}}

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10889676
|overall_frequency_n=42
|overall_frequency_d=128
|overall_frequency=0.328125
|n_genomes=28
|n_genomes_annotated=0
|n_haplomes=35
|n_articles=0
|n_articles_annotated=0
|in_pharmgkb=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}