{{Rsnum
|rsid=348601
|Chromosome=5
|position=40319904
|Orientation=minus
|GMAF=0.477
|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 | 37.2 | 48.7 | 14.2
| HCB | 3.6 | 24.1 | 72.3
| JPT | 0.9 | 24.8 | 74.3
| YRI | 41.4 | 44.8 | 13.8
| ASW | 47.4 | 42.1 | 10.5
| CHB | 3.6 | 24.1 | 72.3
| CHD | 1.8 | 24.8 | 73.4
| GIH | 15.8 | 44.6 | 39.6
| LWK | 57.3 | 33.6 | 9.1
| MEX | 22.4 | 46.6 | 31.0
| MKK | 40.0 | 41.3 | 18.7
| TSI | 31.4 | 52.0 | 16.7
| HapMapRevision=28
}}

rs348601 increases susceptibility to Crohn's disease 1.36 times for carriers of the A allele {{PMID|17447842|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}