{{Rsnum
|rsid=11209003
|Gene=C1orf141
|Chromosome=1
|position=67135449
|Orientation=plus
|GMAF=0.2957
|Gene_s=C1orf141
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 48.7 | 44.2 | 7.1
| HCB | 48.9 | 41.6 | 9.5
| JPT | 52.2 | 42.5 | 5.3
| YRI | 77.6 | 22.4 | 0.0
| ASW | 61.4 | 38.6 | 0.0
| CHB | 48.9 | 41.6 | 9.5
| CHD | 49.5 | 41.3 | 9.2
| GIH | 45.5 | 44.6 | 9.9
| LWK | 48.2 | 46.4 | 5.5
| MEX | 17.2 | 50.0 | 32.8
| MKK | 38.5 | 40.4 | 21.2
| TSI | 56.4 | 40.6 | 3.0
| HapMapRevision=28
}}{{GWAS Summary
|SNP=rs11209003
|PubMedID=17804789
|Condition=Crohn's disease
|Gene=IL23R
|Risk Allele=
|pValue=2.00E-007
|OR=2.56
|95CI=1.75-3.70
|OA=1
}}

{{PharmGKB
|RSID=rs11209003
|Name_s=
|Gene_s=C1orf141
|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=PA162356486
}}

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs11209003
|overall_frequency_n=35
|overall_frequency_d=128
|overall_frequency=0.273438
|n_genomes=24
|n_genomes_annotated=0
|n_haplomes=29
|n_articles=0
|n_articles_annotated=0
|in_pharmgkb=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}