{{Rsnum
|rsid=348594
|Chromosome=5
|position=40323836
|Orientation=plus
|GMAF=0.4917
|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 | 38.1 | 50.4 | 11.5
| HCB | 4.4 | 24.1 | 71.5
| JPT | 0.9 | 24.8 | 74.3
| YRI | 51.7 | 38.8 | 9.5
| ASW | 50.9 | 40.4 | 8.8
| CHB | 4.4 | 24.1 | 71.5
| CHD | 0.9 | 28.4 | 70.6
| GIH | 17.8 | 44.6 | 37.6
| LWK | 60.0 | 31.8 | 8.2
| MEX | 22.4 | 50.0 | 27.6
| MKK | 47.4 | 39.1 | 13.5
| TSI | 32.4 | 51.0 | 16.7
| HapMapRevision=28
}}{{Report GE
|PubMed=17447842
|Source=pubmed
|AffyProbeset=SNP_A-8391321
|AffyOrientation=same
|AlleleA=A
|AlleleB=G
|onGW5=0
|rsid=348594
|ancestral=G
|RiskPopulation=EU
|RiskAllele=A
|CaseFreq=0.67
|ControlFreq=0.6
|OddsRatioHet=
|OddsRatioHom=
|OddsRatioAll=1.36
|Disease=Crohn's disease
|DiseaseSymbol=CD
|OA=1
}}

rs348594 is in linkage disequilibrium with a polymorphism that increases susceptibility to Crohn's disease 1.36 times for carriers of the A allele {{PMID|17447842|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}