{{Rsnum
|rsid=7807268
|Chromosome=7
|position=148560956
|Orientation=plus
|GMAF=0.4931
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 31.0 | 47.8 | 21.2
| HCB | 15.3 | 53.3 | 31.4
| JPT | 10.6 | 40.7 | 48.7
| YRI | 21.1 | 44.9 | 34.0
| ASW | 26.3 | 35.1 | 38.6
| CHB | 15.3 | 53.3 | 31.4
| CHD | 18.3 | 47.7 | 33.9
| GIH | 20.8 | 46.5 | 32.7
| LWK | 39.1 | 44.5 | 16.4
| MEX | 22.4 | 41.4 | 36.2
| MKK | 41.7 | 45.5 | 12.8
| TSI | 30.4 | 45.1 | 24.5
| HapMapRevision=28
}}[[rs7807268]] has been reported in a large study to be associated with [[Crohn's disease]].

The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 1.38 (CI 1.20-1.60), and for homozygotes, 1.47 (CI 1.24-1.74). {{PMID|17554300|OA=1
}}

* Note: there is a slight amount of ambiguity over the orientation of this SNP information relative to the dbSNP entry.

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7807268
|overall_frequency_n=65
|overall_frequency_d=128
|overall_frequency=0.507812
|n_genomes=39
|n_genomes_annotated=0
|n_haplomes=52
|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}}