{{Rsnum
|rsid=11989782
|Gene=SNTB1
|Chromosome=8
|position=120682410
|Orientation=plus
|GMAF=0.14
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=SNTB1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 5.4 | 32.1 | 62.5
| HCB | 0.0 | 17.9 | 82.1
| JPT | 0.0 | 26.5 | 73.5
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 5.4 | 94.6
| CHB | 0.0 | 17.9 | 82.1
| CHD | 0.0 | 10.3 | 89.7
| GIH | 0.0 | 19.8 | 80.2
| LWK | 0.0 | 3.6 | 96.4
| MEX | 1.8 | 29.8 | 68.4
| MKK | 0.0 | 9.0 | 91.0
| TSI | 2.9 | 31.4 | 65.7
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=20208534
|Trait=Eosinophilic esophagitis (pediatric)
|Title=Common variants at 5q22 associate with pediatric eosinophilic esophagitis
|RiskAllele=A
|Pval=0.000007
|OR=1.53
|ORtxt=[1.21-1.93]
|OA=1
}}

{{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}}