{{Rsnum
|rsid=1939875
|Chromosome=11
|position=95689703
|Orientation=minus
|GMAF=0.253
|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 | 47.8 | 38.9 | 13.3
| HCB | 55.5 | 40.1 | 4.4
| JPT | 60.2 | 33.6 | 6.2
| YRI | 58.9 | 38.4 | 2.7
| ASW | 61.4 | 31.6 | 7.0
| CHB | 55.5 | 40.1 | 4.4
| CHD | 53.2 | 39.4 | 7.3
| GIH | 48.5 | 38.6 | 12.9
| LWK | 76.4 | 21.8 | 1.8
| MEX | 63.8 | 36.2 | 0.0
| MKK | 80.8 | 17.9 | 1.3
| TSI | 55.9 | 39.2 | 4.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20208534
|Trait=Eosinophilic esophagitis (pediatric)
|Title=Common variants at 5q22 associate with pediatric eosinophilic esophagitis
|RiskAllele=T
|Pval=0.000003
|OR=1.54
|ORtxt=[1.22-1.93]
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}