{{Rsnum
|rsid=13106227
|Gene=SHROOM3
|Chromosome=4
|position=76497528
|Orientation=plus
|GMAF=0.4477
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=SHROOM3
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 45.5 | 42.0 | 12.5
| HCB | 30.5 | 51.1 | 18.3
| JPT | 28.9 | 40.0 | 31.1
| YRI | 13.2 | 50.0 | 36.8
| ASW | 14.5 | 60.0 | 25.5
| CHB | 30.5 | 51.1 | 18.3
| CHD | 30.6 | 51.9 | 17.6
| GIH | 43.6 | 39.6 | 16.8
| LWK | 12.3 | 47.2 | 40.6
| MEX | 35.1 | 56.1 | 8.8
| MKK | 0.0 | 0.0 | 0.0
| TSI | 40.6 | 43.6 | 15.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20208534
|Trait=Eosinophilic esophagitis (pediatric)
|Title=Common variants at 5q22 associate with pediatric eosinophilic esophagitis
|RiskAllele=
|Pval=0.000004
|OR=1.52
|ORtxt=[1.20-1.92]
|OA=1
}}

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