{{Rsnum
|rsid=2224865
|Chromosome=10
|position=85422854
|Orientation=plus
|GMAF=0.3531
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 14.2 | 49.6 | 36.3
| HCB | 16.8 | 46.7 | 36.5
| JPT | 16.1 | 49.1 | 34.8
| YRI | 18.5 | 54.8 | 26.7
| ASW | 24.6 | 40.4 | 35.1
| CHB | 16.8 | 46.7 | 36.5
| CHD | 14.8 | 43.5 | 41.7
| GIH | 5.0 | 49.5 | 45.5
| LWK | 23.6 | 40.9 | 35.5
| MEX | 3.4 | 20.7 | 75.9
| MKK | 18.7 | 56.1 | 25.2
| TSI | 7.9 | 37.6 | 54.5
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20208534
|Trait=Eosinophilic esophagitis (pediatric)
|Title=Common variants at 5q22 associate with pediatric eosinophilic esophagitis
|RiskAllele=G
|Pval=0.000009
|OR=1.44
|ORtxt=[1.15-1.79]
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}