{{Rsnum
|rsid=6601764
|Chromosome=10
|position=3862542
|Orientation=plus
|GMAF=0.3669
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 18.6 | 54.9 | 26.5
| HCB | 60.6 | 35.8 | 3.6
| JPT | 50.4 | 39.8 | 9.7
| YRI | 63.9 | 32.7 | 3.4
| ASW | 43.9 | 47.4 | 8.8
| CHB | 60.6 | 35.8 | 3.6
| CHD | 62.4 | 35.8 | 1.8
| GIH | 43.6 | 45.5 | 10.9
| LWK | 52.7 | 41.8 | 5.5
| MEX | 36.2 | 50.0 | 13.8
| MKK | 46.8 | 41.7 | 11.5
| TSI | 17.6 | 54.9 | 27.5
| HapMapRevision=28
}}
[[rs6601764]] has been reported in a large study to be associated with [[Crohn's disease]].

The risk allele (oriented to the dbSNP entry) is (C); the odds ratio associated with heterozygotes is 1.16 (CI 1.01-1.33), and for homozygotes, 1.52 (CI 1.28-1.80). {{PMID|17554300|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6601764
|overall_frequency_n=58
|overall_frequency_d=128
|overall_frequency=0.453125
|n_genomes=33
|n_genomes_annotated=0
|n_haplomes=45
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}