{{Rsnum
|rsid=371915
|Chromosome=16
|position=84544635
|Orientation=plus
|GMAF=0.1405
|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 | 0.9 | 16.8 | 82.3
| HCB | 2.2 | 12.4 | 85.4
| JPT | 2.7 | 23.9 | 73.5
| YRI | 2.1 | 24.7 | 73.3
| ASW | 1.8 | 26.3 | 71.9
| CHB | 2.2 | 12.4 | 85.4
| CHD | 0.0 | 18.3 | 81.7
| GIH | 5.9 | 36.6 | 57.4
| LWK | 2.7 | 30.9 | 66.4
| MEX | 6.9 | 22.4 | 70.7
| MKK | 1.9 | 22.4 | 75.6
| TSI | 2.0 | 20.6 | 77.5
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20208534
|Trait=Eosinophilic esophagitis (pediatric)
|Title=Common variants at 5q22 associate with pediatric eosinophilic esophagitis
|RiskAllele=
|Pval=2E-8
|OR=1.90
|ORtxt=[1.44-2.50]
|OA=1
}}

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