{{Rsnum
|rsid=6501384
|Chromosome=17
|position=70294992
|Orientation=plus
|GMAF=0.2934
|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 | 42.0 | 48.2 | 9.8
| HCB | 62.8 | 35.8 | 1.5
| JPT | 69.0 | 29.2 | 1.8
| YRI | 34.7 | 48.3 | 17.0
| ASW | 38.6 | 56.1 | 5.3
| CHB | 62.8 | 35.8 | 1.5
| CHD | 70.6 | 25.7 | 3.7
| GIH | 29.7 | 49.5 | 20.8
| LWK | 48.6 | 42.2 | 9.2
| MEX | 56.9 | 41.4 | 1.7
| MKK | 44.2 | 40.4 | 15.4
| TSI | 38.2 | 46.1 | 15.7
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=20208534
|Trait=Eosinophilic esophagitis (pediatric)
|Title=Common variants at 5q22 associate with pediatric eosinophilic esophagitis
|RiskAllele=T
|Pval=0.000006
|OR=1.41
|ORtxt=[1.13-1.76]
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}