{{Rsnum
|rsid=7236477
|Gene=DSG1
|Chromosome=18
|position=31322359
|Orientation=plus
|GMAF=0.06382
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=DSG1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 88.5 | 11.5 | 0.0
| HCB | 93.4 | 5.8 | 0.7
| JPT | 95.6 | 4.4 | 0.0
| YRI | 79.6 | 19.0 | 1.4
| ASW | 84.2 | 14.0 | 1.8
| CHB | 93.4 | 5.8 | 0.7
| CHD | 93.6 | 5.5 | 0.9
| GIH | 69.3 | 28.7 | 2.0
| LWK | 77.3 | 22.7 | 0.0
| MEX | 82.8 | 15.5 | 1.7
| MKK | 70.5 | 26.3 | 3.2
| TSI | 91.2 | 8.8 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20208534
|Trait=Eosinophilic esophagitis (pediatric)
|Title=Common variants at 5q22 associate with pediatric eosinophilic esophagitis
|RiskAllele=G
|Pval=0.000007
|OR=2.22
|ORtxt=[1.39-3.55]
|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}}