{{Rsnum
|rsid=924080
|Chromosome=1
|position=67294457
|Orientation=plus
|GMAF=0.3972
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 25.0 | 47.3 | 27.7
| HCB | 1.5 | 39.7 | 58.8
| JPT | 8.0 | 38.4 | 53.6
| YRI | 22.4 | 46.3 | 31.3
| ASW | 21.1 | 57.9 | 21.1
| CHB | 1.5 | 39.7 | 58.8
| CHD | 5.5 | 31.2 | 63.3
| GIH | 5.9 | 51.5 | 42.6
| LWK | 23.9 | 50.5 | 25.7
| MEX | 15.8 | 56.1 | 28.1
| MKK | 20.1 | 50.0 | 29.9
| TSI | 22.0 | 48.0 | 30.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20622878
|Trait=Behcet's disease
|Title=Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease
|RiskAllele=
|Pval=7E-9
|OR=1.28
|ORtxt=[1.18-1.39]
|OA=1
}}

{{PMID Auto
|PMID=17068223
|Title=A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
}}

{{PMID Auto
|PMID=22076442
|Title=A GWAS follow-up study reveals the association of the IL12RB2 gene with systemic sclerosis in Caucasian populations.
|OA=1
}}

{{PMID Auto
|PMID=22378604
|Title=Association study of IL10 and IL23R-IL12RB2 in Iranian patients with Behcet's disease.
}}

{{PMID Auto
|PMID=24151497
|Title=Association Analysis of IL10, TNF-α, and IL23R-IL12RB2 SNPs with Behçet's Disease Risk in Western Algeria
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}