{{Rsnum
|rsid=11747270
|Chromosome=5
|position=150879305
|Orientation=plus
|GMAF=0.2828
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 90.3 | 9.7 | 0.0
| HCB | 34.3 | 48.9 | 16.8
| JPT | 40.7 | 42.5 | 16.8
| YRI | 20.4 | 52.4 | 27.2
| ASW | 28.1 | 47.4 | 24.6
| CHB | 34.3 | 48.9 | 16.8
| CHD | 27.5 | 54.1 | 18.3
| GIH | 72.3 | 24.8 | 3.0
| LWK | 35.8 | 46.8 | 17.4
| MEX | 72.4 | 24.1 | 3.4
| MKK | 51.3 | 39.7 | 9.0
| TSI | 71.6 | 27.5 | 1.0
| HapMapRevision=28
}}{{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=G
|Pval=2.9999999999999999E-16
|OR=1.33
|ORtxt=[NR]
|OA=1
}}

{{omim
|desc=INFLAMMATORY BOWEL DISEASE 19; IBD19
|id=612278
|rsnum=11747270
}}

{{PMID Auto
|PMID=19557189
|Title=Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions.
|OA=1
}}

{{PMID Auto
|PMID=20106866
|Title=Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease.
|OA=1
}}

{{PMID Auto
|PMID=22065112
|Title=The JAK2 variant rs10758669 in Crohn's disease: altering the intestinal barrier as one mechanism of action.
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs11747270
|overall_frequency_n=36
|overall_frequency_d=126
|overall_frequency=0.285714
|n_genomes=25
|n_genomes_annotated=0
|n_haplomes=33
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}