{{Rsnum
|rsid=1986734
|Gene=SHROOM3
|Chromosome=4
|position=76499631
|Orientation=plus
|GMAF=0.4371
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SHROOM3
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 21.6 | 49.5 | 28.8
| HCB | 24.4 | 44.4 | 31.1
| JPT | 20.2 | 58.7 | 21.1
| YRI | 73.0 | 23.8 | 3.2
| ASW | 48.1 | 48.1 | 3.7
| CHB | 24.4 | 44.4 | 31.1
| CHD | 0.0 | 0.0 | 0.0
| GIH | 29.6 | 49.0 | 21.4
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 51.6 | 45.1 | 3.3
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20208534
|Trait=Eosinophilic esophagitis (pediatric)
|Title=Common variants at 5q22 associate with pediatric eosinophilic esophagitis
|RiskAllele=
|Pval=0.000001
|OR=1.54
|ORtxt=[1.22-1.89]
|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}}