{{Rsnum
|rsid=3806932
|Gene=TSLP
|Chromosome=5
|position=111069977
|Orientation=plus
|GMAF=0.4692
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=TSLP
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 29.5 | 50.9 | 19.6
| HCB | 40.7 | 48.1 | 11.1
| JPT | 51.4 | 42.3 | 6.3
| YRI | 14.0 | 43.4 | 42.7
| ASW | 17.9 | 41.1 | 41.1
| CHB | 40.7 | 48.1 | 11.1
| CHD | 0.0 | 0.0 | 0.0
| GIH | 6.2 | 51.5 | 42.3
| LWK | 13.1 | 47.7 | 39.3
| MEX | 34.5 | 37.9 | 27.6
| MKK | 13.9 | 45.0 | 41.1
| TSI | 29.9 | 51.5 | 18.6
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20208534
|Trait=Eosinophilic esophagitis (pediatric)
|Title=Common variants at 5q22 associate with pediatric eosinophilic esophagitis
|RiskAllele=
|Pval=3E-9
|OR=1.85
|ORtxt=None
|OA=1
}}

{{omim
|id=613412
|rsnum=3806932
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}