{{Rsnum
|rsid=11209026
|Gene=IL23R
|Chromosome=1
|position=67240275
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0.03306
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=IL23R
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 8.2 | 91.8
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 3.2 | 96.8
| ASW | 0.0 | 3.5 | 96.5
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.9 | 99.1
| GIH | 0.0 | 1.0 | 99.0
| LWK | 0.0 | 1.0 | 99.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.7 | 5.9 | 93.5
| TSI | 1.0 | 15.2 | 83.8
| HapMapRevision=28
}}{{CPMC SNP
|link=http://cpmc1.coriell.org/about-the-cpmc-study/health-conditions-and-drug-response/ulcerative-colitis/cpmc-and-ulcerative-colitis
}}

A relatively rare allele at SNP [[rs11209026]], in the [[IL23R]] gene, appears to provide a fairly strong protective effect against the development of [[Crohn's disease]] in both Jewish and non-Jewish populations. {{PMID|17068223}}

Note that in this study the (A;A) and (A;G) genotypes were combined for statistical reasons (there were too few (A;A) individuals to study by themselves), so the risk is shown as equal for both.

{{PMID|18047540}} associated With Inflammatory Bowel Diseases but Not With Celiac Disease
[[rs11209026]] had a protective effect for IBD in the case-control analysis (odds ratio [OR] 0.19, 95% confidence interval [CI] 0.10-0.37, P= 6.6E-09). Both CD (OR 0.14, CI 0.06-0.37, P= 3.9E-07) and UC (OR 0.33, CI 0.15-0.73, P= 1.4E-03) were associated with IL23R. [[rs2241880]] was associated with CD susceptibility (OR 1.36, CI 1.12-1.66, P= 0.0017). The population-attributable risk of carrying allele G is 0.24 and is 0.19 for homozygosity for allele G in CD.

With reference to [[ankylosing spondylitis]], the [[rs11209026]](A) allele also has a protective effect. The odds ratio for carriers is 0.63 (p=2.8x10e-5) based on a large study of over 1,000 Caucasian patients.[PMID 17952073, PMID 18037607]

This SNP is also part of a haplotype with [[rs7530511]] associated with [[psoriasis]].{{PMID|18219280|OA=1
}}. And in {{PMID|18369459|OA=1
}} [[rs11209026]] was also confirmed to be associated with [[psoriasis]].

{{PMID|18047539}} significant associations with [[rs1004819]], [[rs7517847]], and [[rs11209026]]. Having any CARD15 variant was associated with a significant risk for CD (P < 0.0001). 

{{PMID|18698678|OA=1
}} Replicated reduced risk for [[Crohn's disease]] and [[ulcerative colitis]] with [[rs11209026]](A) allele in a study of Italian patients.

A genome-wide association study using DNA samples from 1,052 individuals with [[ulcerative colitis]] and preexisting data from 2,571 controls, all of European ancestry, concluded that this SNP and several others were associated with altered risk for the disease.{{PMID|19122664|OA=1
}}

{{GWAS Summary
|SNP=rs11209026
|PubMedID=17068223
|Condition=Inflammatory bowel disease
|Gene=IL23R
|Risk Allele=A
|pValue=4.00E-011
|OR=3.84
|95CI=2.33-6.66
}}
{{PMID Auto
|PMID=19174780
|Title=Confirmation of multiple Crohn's disease susceptibility loci in a large Dutch-Belgian cohort
}}

{{PMID Auto GWAS
|PMID=18758464
|Trait=Inflammatory bowel disease
|Title=Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease
|RiskAllele=
|Pval=7.0000000000000004E-11
|OR=2.56
|ORtxt=[1.92-3.45]
|OA=1
}}
{{PMID Auto GWAS
|PMID=17447842
|Trait=Crohn's disease
|Title=Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4
|RiskAllele=
|Pval=2.0000000000000001E-18
|OR=2.92
|ORtxt=[NR]
|OA=1
}}

{{omim
|id=612261
|desc=INFLAMMATORY BOWEL DISEASE 17; IBD17
|rsnum=11209026
}}

{{omim
|id=607562
|desc=INTERLEUKIN 23 RECEPTOR; IL23R
|rsnum=11209026
}}
{{PMID Auto
|PMID=19590455
|Title=Association of IL23R p.381Gln and ATG16L1 p.197Ala With Crohn Disease in the Czech Population
}}
{{PMID Auto
|PMID=19877036
|Title=Association of ERAP1, but not IL23R, with ankylosing spondylitis in a Han Chinese population
}}

{{PharmGKB
|RSID=rs11209026
|Name_s=
|Gene_s=IL23R
|Feature=
|Evidence=PubMed ID:19122664; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. (Initial Sample Size: 1,022 cases, 2,503 controls; Replication Sample Size: 1,387 cases, 1,115 controls); (Region: 1p31.3; Reported Gene(s): IL23R; Risk Allele: rs11209026-?); (p-value= 0.00000001).This variant is associated with Ulcerative colitis.
|Drugs=
|Drug Classes=
|Diseases=Colitis, Ulcerative
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164740085
}}
{{PMID Auto GWAS
|PMID=19915572
|Trait=Ulcerative colitis
|Title=Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region
|RiskAllele=
|Pval=3E-10
|OR=NR
|ORtxt=NR
|OA=1
}}

{{PMID Auto GWAS
|PMID=20062062
|Trait=Ankylosing spondylitis
|Title=Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci
|RiskAllele=
|Pval=9E-14
|OR=1.89
|ORtxt=[1.56-2.27]
|OA=1
}}

{{PMID Auto
|PMID=20157760
|Title=Interleukin-23 receptor genetic polymorphisms and Crohn's disease susceptibility: a meta-analysis
}}
{{PMID Auto
|PMID=19705136
|Title=Genetic evidence for involvement of the IL23 pathway in Thai psoriatics
|OA=1
}}

{{PMID Auto
|PMID=20380008
|Title=NOD2/CARD15, ATG16L1 and IL23R gene polymorphisms and childhood-onset of Crohn's disease
|OA=1
}}
{{PMID Auto
|PMID=20537165
|Title=The CTLA4 variants may interact with the IL23R- and NOD2-conferred risk in development of Crohn's disease
|OA=1
}}
{{PMID Auto
|PMID=20485703
|Title=Replication and meta-analysis of 13,000 cases defines the risk for interleukin-23 receptor and autophagy-related 16-like 1 variants in Crohn's disease
|OA=1
}}
{{PMID Auto
|PMID=20650992
|Title=Association of IBD Risk Loci with Sarcoidosis and its Acute and Chronic Subphenotypes
}}

{{PharmGKB
|RSID=rs11209026
|Name_s=IL23R:Arg381Gln
|Gene_s=IL23R
|Feature=
|Evidence=PubMed ID:17068223
|Annotation=The A allele of rs11209026 was shown to be associated with protection from Crohn's disease in GWAS of two white case-control cohorts(one Jewish, one non-Jewish).
|Drugs=
|Drug Classes=
|Diseases=Crohn Disease
|Curation Level=Curated
|PharmGKB Accession ID=PA161889365
}}

{{PharmGKB
|RSID=rs11209026
|Name_s=
|Gene_s=IL23R
|Feature=
|Evidence=PubMed ID:17068223; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS Results: A genome-wide association study identifies IL23R as an inflammatory bowel disease gene (Initial Sample Size: 547 cases, 548 controls; Replication Sample Size: 401 cases, 433 controls, 883 families, 1,119 affected offspring; Risk Allele: rs11209026-A).
|Drugs=
|Drug Classes=
|Diseases=Inflammatory Bowel Diseases
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA162356595
}}

{{PharmGKB
|RSID=rs11209026
|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=PA162356493
}}
{{PMID Auto
|PMID=21206965
|Title=IL23R, NOD2/CARD15, ATG16L1 and PHOX2B polymorphisms in a group of patients with Crohn's disease and correlation with sub-phenotypes
}}

{{PMID Auto GWAS
|PMID=21102463
|Trait=None
|Title=Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
|RiskAllele=G
|Pval=1E-64
|OR=2.6600
|ORtxt=[2.36-3.00]
|OA=1
}}
{{PMID Auto GWAS
|PMID=20953190
|Trait=None
|Title=A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1
|RiskAllele=
|Pval=7E-7
|OR=1.4900
|ORtxt=[1.27-1.74]
|OA=1
}}
{{omim
|id=607562
|rsnum=11209026
|variant=0001
}}

{{PMID Auto GWAS
|PMID=21297633
|Trait=None
|Title=Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
|RiskAllele=G
|Pval=5E-28
|OR=1.7400
|ORtxt=[1.57-1.92]
|OA=1
}}

{{PMID Auto GWAS
|PMID=21743469
|Trait=None
|Title=Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.
|RiskAllele=G
|Pval=2E-17
|OR=None
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=22089529
|Title=Associations between interleukin-23R polymorphisms and ankylosing spondylitis susceptibility: a meta-analysis
}}

{{PMID Auto
|PMID=22130325
|Title=IL-23R rs11209026 polymorphism modulates IL-17A expression in patients with rheumatoid arthritis
}}

{{PMID Auto
|PMID=22440928
|Title=Perianal Crohn's Disease: Predictive Factors and Genotype-Phenotype Correlations
|OA=1
}}

{{PMID Auto
|PMID=21896776
|Title=Role of Interleukin-23 (IL-23) Receptor Signaling for IL-17 Responses in Human Lyme Disease.
|OA=1
}}

{{PMID Auto
|PMID=22695161
|Title=IL23R Arg381Gln functional polymorphism associated with active pulmonary tuberculosis severity
|OA=1
}}

{{PMID Auto GWAS
|PMID=22412388
|Trait=None
|Title=A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.
|RiskAllele=G
|Pval=1E-18
|OR=2.2000
|ORtxt=None
|OA=1
}}

{{PMID Auto GWAS
|PMID=22293688
|Trait=None
|Title=1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data.
|RiskAllele=
|Pval=4E-21
|OR=3.1800
|ORtxt=None
|OA=1
}}

{{ClinVar
|rsid=11209026
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=67240275
|CHROM=1
|GMAF=0.033
|dbSNPBuildID=120
|SSR=0
|SAO=1
|VP=0x050168000a05150517130100
|GENEINFO=IL23R:149233
|GENE_NAME=IL23R
|GENE_ID=149233
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.67240275G>A
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;PMC;SLO;NSM;REF;ASP;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;MTP;OM
|CAF=0.9669; 0.03306
|CLNACC=RCV000003254.2; RCV000003255.2
|CLNDBN=Inflammatory bowel disease 17, protection against; Psoriasis, protection against
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_144701.2:c.1142G>A; 607562.0001
|COMMON=1
|Disease=Inflammatory bowel disease 17; Psoriasis
}}

{{PMID Auto
|PMID=17236132
|Title=A large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genes.
|OA=1
}}

{{PMID Auto
|PMID=17508420
|Title=Contribution of the novel inflammatory bowel disease gene IL23R to disease susceptibility and phenotype.
}}

{{PMID Auto
|PMID=17618837
|Title=Association of variants of the interleukin-23 receptor gene with susceptibility to pediatric Crohn's disease.
}}

{{PMID Auto
|PMID=17678723
|Title=Investigation of the IL23R gene in a Spanish rheumatoid arthritis cohort.
}}

{{PMID Auto
|PMID=17678845
|Title=Replication of an association between IL23R gene polymorphism with inflammatory bowel disease.
}}

{{PMID Auto
|PMID=17684544
|Title=Systematic association mapping identifies NELL1 as a novel IBD disease gene.
|OA=1
}}

{{PMID Auto
|PMID=17786191
|Title=rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants.
|OA=1
}}

{{PMID Auto
|PMID=17877509
|Title=Heterozygosity for IL23R p.Arg381Gln confers a protective effect not only against Crohn's disease but also ulcerative colitis.
}}

{{PMID Auto
|PMID=17894849
|Title=IL23R R381Q and ATG16L1 T300A are strongly associated with Crohn's disease in a study of New Zealand Caucasians with inflammatory bowel disease.
}}

{{PMID Auto
|PMID=17901940
|Title=Association analysis of IL-12B and IL-23R polymorphisms in myocardial infarction.
}}

{{PMID Auto
|PMID=17940599
|Title=Assembly of inflammation-related genes for pathway-focused genetic analysis.
|OA=1
}}

{{PMID Auto
|PMID=18045485
|Title=The candidate genes TAF5L, TCF7, PDCD1, IL6 and ICAM1 cannot be excluded from having effects in type 1 diabetes.
|OA=1
}}

{{PMID Auto
|PMID=18073300
|Title=Interleukin (IL)-23 receptor is a major susceptibility gene for Graves' ophthalmopathy: the IL-23/T-helper 17 axis extends to thyroid autoimmunity.
|OA=1
}}

{{PMID Auto
|PMID=18199597
|Title=The IL23R Arg381Gln non-synonymous polymorphism confers susceptibility to ankylosing spondylitis.
}}

{{PMID Auto
|PMID=18200510
|Title=CARD15 and IL23R influences Crohn's disease susceptibility but not disease phenotype in a Brazilian population.
}}

{{PMID Auto
|PMID=18224312
|Title=Pharmacogenetics: data, concepts and tools to improve drug discovery and drug treatment.
|OA=1
}}

{{PMID Auto
|PMID=18368064
|Title=IL23R: a susceptibility locus for celiac disease and multiple sclerosis?
}}

{{PMID Auto
|PMID=18383363
|Title=Association of interleukin-23 receptor variants with ankylosing spondylitis.
}}

{{PMID Auto
|PMID=18383521
|Title=IL23R and IL12B polymorphisms in Spanish IBD patients: no evidence of interaction.
}}

{{PMID Auto
|PMID=18438406
|Title=Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease.
|OA=1
}}

{{PMID Auto
|PMID=18470928
|Title=IL23R haplotypes provide a large population attributable risk for Crohn's disease.
|OA=1
}}

{{PMID Auto
|PMID=18499543
|Title=ATG16L1 and IL23 receptor (IL23R) genes are associated with disease susceptibility in Hungarian CD patients.
}}

{{PMID Auto
|PMID=18609743
|Title=Genetics of psoriasis and psoriatic arthritis: update and future direction.
|OA=1
}}

{{PMID Auto
|PMID=18647855
|Title=Evidence for association of an interleukin 23 receptor variant independent of the R381Q variant with rheumatoid arthritis.
}}

{{PMID Auto
|PMID=18715515
|Title=Lack of evidence for association of primary sclerosing cholangitis and primary biliary cirrhosis with risk alleles for Crohn's disease in Polish patients.
|OA=1
}}

{{PMID Auto
|PMID=18800148
|Title=Genetic variants of the IL-23R pathway: association with psoriatic arthritis and psoriasis vulgaris, but no specific risk factor for arthritis.
}}

{{PMID Auto
|PMID=19021011
|Title=Association studies of the IL-23R gene in autoimmune thyroid disease in the Japanese population.
}}

{{PMID Auto
|PMID=19035472
|Title=Investigation of association of the IL12B and IL23R genes with psoriatic arthritis.
|OA=1
}}

{{PMID Auto
|PMID=19040306
|Title=Association of interleukin 23 receptor variants with psoriatic arthritis.
}}

{{PMID Auto
|PMID=19103525
|Title=IL-23R Arg381Gln polymorphism in Chilean patients with inflammatory bowel disease.
}}

{{PMID Auto
|PMID=19161620
|Title=An open access database of genome-wide association results.
|OA=1
}}

{{PMID Auto
|PMID=19165485
|Title=Interleukin-23 receptor (IL-23R) gene polymorphisms in acquired aplastic anemia.
|OA=1
}}

{{PMID Auto
|PMID=19175939
|Title=IL23R in the Swedish, Finnish, Hungarian and Italian populations: association with IBD and psoriasis, and linkage to celiac disease.
|OA=1
}}

{{PMID Auto
|PMID=19182814
|Title=New insights into the pathogenesis and genetics of psoriatic arthritis.
|OA=1
}}

{{PMID Auto
|PMID=19189980
|Title=Association between the interleukin 23 receptor and ankylosing spondylitis is confirmed by a new UK case-control study and meta-analysis of published series.
}}

{{PMID Auto
|PMID=19294505
|Title=Genetic association of nonsynonymous variants of the IL23R with familial and sporadic inflammatory bowel disease in women.
}}

{{PMID Auto
|PMID=19468064
|Title=Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions.
|OA=1
}}

{{PMID Auto
|PMID=19522770
|Title=Variants of the IL23R gene are associated with ankylosing spondylitis but not with Sjogren syndrome in Hungarian population samples.
}}

{{PMID Auto
|PMID=19918037
|Title=Association of interleukin 23 receptor polymorphisms with anti-topoisomerase-I positivity and pulmonary hypertension in systemic sclerosis.
|OA=1
}}

{{PMID Auto
|PMID=20082483
|Title=NOD2, IL23R and ATG16L1 polymorphisms in Lithuanian patients with inflammatory bowel disease.
|OA=1
}}

{{PMID Auto
|PMID=20173782
|Title=Prognostic significance of genetic variants in the IL-23/Th17 pathway for the outcome of T cell-depleted allogeneic stem cell transplantation.
}}

{{PMID Auto
|PMID=20192940
|Title=Association of the interleukin-23 receptor gene variant rs11209026 with Crohn's disease in German children.
}}

{{PMID Auto
|PMID=20444268
|Title=Peripheral blood gene expression patterns discriminate among chronic inflammatory diseases and healthy controls and identify novel targets.
|OA=1
}}

{{PMID Auto
|PMID=20454450
|Title=Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset.
|OA=1
}}

{{PMID Auto
|PMID=20606885
|Title=Genetics of psoriasis and psoriatic arthritis.
|OA=1
}}

{{PMID Auto
|PMID=21253733
|Title=Interleukin-23 receptor genetic polymorphisms and ankylosing spondylitis susceptibility: a meta-analysis.
}}

{{PMID Auto
|PMID=21281511
|Title=Subtype specific genetic associations for juvenile idiopathic arthritis: ERAP1 with the enthesitis related arthritis subtype and IL23R with juvenile psoriatic arthritis.
|OA=1
}}

{{PMID Auto
|PMID=21304977
|Title=An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians.
|OA=1
}}

{{GET Evidence
|gene=IL23R
|aa_change=Arg381Gln
|aa_change_short=R381Q
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs11209026
|overall_frequency_n=513
|overall_frequency_d=10756
|overall_frequency=0.0476943
|n_genomes=3
|n_genomes_annotated=0
|n_haplomes=4
|n_articles=1
|n_articles_annotated=1
|in_omim=Y
|in_gwas=Y
|in_pharmgkb=Y
|pph2_score=0.997
|nblosum100=0
|autoscore=4
|webscore=N
}}

{{PMID Auto
|PMID=23093722
|Title=Exploring ankylosing spondylitis-associated ERAP1, IL23R and IL12B gene polymorphisms in subphenotypes of psoriatic arthritis
}}

{{PMID Auto GWAS
  |PMID=23128233
  |Trait=Inflammatory bowel disease
  |Title=Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
  |RiskAllele=G
  |Pval=8E-161
  |OR=2.01
  |ORtxt=[1.885-2.15]
  |OA=1
}}

{{PMID Auto GWAS
  |PMID=22936669
  |Trait=Crohn's disease
  |Title=A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.
  |RiskAllele=G
  |Pval=4E-14
  |OR=2.84
  |ORtxt=[NR]
  }}

{{PMID Auto
|PMID=23579029
|Title=Protective effect of interleukin-23A (IL23A) haplotype variants on type 1A diabetes mellitus in a Brazilian population
}}

{{PMID Auto
|PMID=23137879
|Title=Evaluation of IL17A expression and of IL17A, IL17F and IL23R gene polymorphisms in Brazilian individuals with periodontitis
}}

{{PMID Auto
|PMID=24140476
|Title=Genetic variations in IL6 and IL12B decreasing the risk for psoriasis
}}

{{PMID Auto
|PMID=22706445
|Title=Association of IL23R polymorphisms with psoriasis and psoriatic arthritis: a meta-analysis.
}}

{{PMID Auto
|PMID=23053963
|Title=Associations between interleukin-23 receptor polymorphisms and susceptibility to rheumatoid arthritis: a meta-analysis.
}}

{{PMID Auto
|PMID=23071489
|Title=SNP-SNP interactions discovered by logic regression explain Crohn's disease genetics.
|OA=1
}}

{{PMID Auto
|PMID=23563201
|Title=The IL23R A/Gln381 allele promotes IL-23 unresponsiveness in human memory T-helper 17 cells and impairs Th17 responses in psoriasis patients.
|OA=1
}}

{{PMID Auto
|PMID=23662788
|Title=The relationship between tumour necrosis factor (TNF)-alpha promoter and IL12B/IL-23R genes polymorphisms and the efficacy of anti-TNF-alpha therapy in psoriasis: a case-control study.
}}

{{PMID Auto
|PMID=23818276
|Title=Brief report: the IL23R nonsynonymous polymorphism rs11209026 is associated with radiographic sacroiliitis in spondyloarthritis.
}}

{{PMID Auto
|PMID=24957500
|Title=Genetic variation at IL12B, IL23R and IL23A is associated with psoriasis severity, psoriatic arthritis and type 2 diabetes mellitus
}}

{{PMID Auto
|PMID=24971461
|Title=Polymorphisms in the Inflammatory Pathway Genes TLR2, TLR4, TLR9, LY96, NFKBIA, NFKB1, TNFA, TNFRSF1A, IL6R, IL10, IL23R, PTPN22, and PPARG Are Associated with Susceptibility of Inflammatory Bowel Disease in a Danish Cohort
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}