{{Rsnum
|rsid=4613763
|Chromosome=5
|position=40392626
|Orientation=plus
|GMAF=0.1097
|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 | 4.4 | 24.8 | 70.8
| HCB | 0.0 | 0.7 | 99.3
| JPT | 0.0 | 0.0 | 100.0
| YRI | 6.1 | 31.3 | 62.6
| ASW | 1.8 | 36.8 | 61.4
| CHB | 0.0 | 0.7 | 99.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 3.0 | 97.0
| LWK | 4.5 | 38.2 | 57.3
| MEX | 0.0 | 8.6 | 91.4
| MKK | 3.8 | 22.4 | 73.7
| TSI | 2.9 | 13.7 | 83.3
| HapMapRevision=28
}}rs4613763 increases susceptibility to Crohn's disease 1.56 times for carriers of the C allele {{PMID|17447842|OA=1
}}

{{ neighbor
| rsid = 2371685
| distance = 502
}}
{{ neighbor
| rsid = 10512734
| distance = 877
}}

{{PMID Auto GWAS
|PMID=18587394
|Trait=Crohn's disease
|Title=Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease
|RiskAllele=C
|Pval=7.0000000000000003E-27
|OR=1.32
|ORtxt=[NR]
|OA=1
}}

{{omim
|desc=INFLAMMATORY BOWEL DISEASE 17; IBD17
|id=612261
|rsnum=4613763
}}

{{omim
|desc=INFLAMMATORY BOWEL DISEASE 18; IBD18
|id=612262
|rsnum=4613763
}}

{{PMID Auto
|PMID=20222910
|Title=Susceptibility loci reported in genome-wide association studies are associated with Crohn's disease in Canadian children
}}

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

{{PMID Auto
|PMID=20018022
|Title=Replication of recently identified associated single-nucleotide polymorphisms from six autoimmune diseases in Genetic Analysis Workshop 16 rheumatoid arthritis data.
|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
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4613763
|overall_frequency_n=19
|overall_frequency_d=128
|overall_frequency=0.148438
|n_genomes=18
|n_genomes_annotated=0
|n_haplomes=18
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{PMID Auto GWAS
  |PMID=21833088
  |Trait=Multiple sclerosis
  |Title=Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
  |RiskAllele=G
  |Pval=3E-16
  |OR=1.20
  |ORtxt=[1.18-1.22]
  |OA=1
}}

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