{{Rsnum
|rsid=6799767
|Chromosome=3
|position=176312308
|Orientation=plus
|GMAF=0.4839
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 17.7 | 46.0 | 36.3
| HCB | 39.4 | 46.7 | 13.9
| JPT | 41.6 | 46.9 | 11.5
| YRI | 40.1 | 43.5 | 16.3
| ASW | 32.1 | 44.6 | 23.2
| CHB | 39.4 | 46.7 | 13.9
| CHD | 46.8 | 42.2 | 11.0
| GIH | 28.7 | 53.5 | 17.8
| LWK | 40.0 | 47.3 | 12.7
| MEX | 27.6 | 46.6 | 25.9
| MKK | 52.6 | 37.2 | 10.3
| TSI | 13.7 | 56.9 | 29.4
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20208534
|Trait=Eosinophilic esophagitis (pediatric)
|Title=Common variants at 5q22 associate with pediatric eosinophilic esophagitis
|RiskAllele=
|Pval=4E-7
|OR=1.49
|ORtxt=[1.18-1.85]
|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}}