{{Rsnum
|rsid=9500256
|Chromosome=6
|position=57982677
|Orientation=plus
|GMAF=0.4803
|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 | 18.6 | 43.4 | 38.1
| HCB | 22.6 | 44.5 | 32.8
| JPT | 25.7 | 55.8 | 18.6
| YRI | 20.4 | 43.5 | 36.1
| ASW | 14.0 | 54.4 | 31.6
| CHB | 22.6 | 44.5 | 32.8
| CHD | 22.9 | 45.9 | 31.2
| GIH | 35.6 | 46.5 | 17.8
| LWK | 12.7 | 39.1 | 48.2
| MEX | 32.8 | 46.6 | 20.7
| MKK | 12.8 | 46.2 | 41.0
| TSI | 19.6 | 57.8 | 22.5
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=20208534
|Trait=Eosinophilic esophagitis (pediatric)
|Title=Common variants at 5q22 associate with pediatric eosinophilic esophagitis
|RiskAllele=
|Pval=0.000005
|OR=2.04
|ORtxt=[1.52-2.70]
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}