{{Rsnum
|rsid=1032757
|Chromosome=5
|position=82643499
|Orientation=plus
|GMAF=0.1887
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 85.8 | 13.3 | 0.9
| HCB | 56.2 | 38.0 | 5.8
| JPT | 62.5 | 32.1 | 5.4
| YRI | 32.9 | 54.8 | 12.3
| ASW | 38.6 | 52.6 | 8.8
| CHB | 56.2 | 38.0 | 5.8
| CHD | 55.6 | 35.2 | 9.3
| GIH | 87.1 | 12.9 | 0.0
| LWK | 41.3 | 47.7 | 11.0
| MEX | 70.2 | 29.8 | 0.0
| MKK | 51.6 | 43.2 | 5.2
| TSI | 85.1 | 14.9 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20208534
|Trait=Eosinophilic esophagitis (pediatric)
|Title=Common variants at 5q22 associate with pediatric eosinophilic esophagitis
|RiskAllele=T
|Pval=0.000002
|OR=1.96
|ORtxt=[1.40-2.74]
|OA=1
}}

{{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}}