{{Rsnum
|rsid=13382811
|Gene=ZEB2
|Chromosome=2
|position=144466053
|Orientation=plus
|GMAF=0.2098
|Gene_s=ZEB2
|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 | 76.8 | 21.4 | 1.8
| HCB | 59.1 | 37.2 | 3.6
| JPT | 55.8 | 36.3 | 8.0
| YRI | 51.7 | 40.8 | 7.5
| ASW | 56.1 | 35.1 | 8.8
| CHB | 59.1 | 37.2 | 3.6
| CHD | 64.8 | 30.6 | 4.6
| GIH | 81.0 | 19.0 | 0.0
| LWK | 58.3 | 36.1 | 5.6
| MEX | 44.8 | 48.3 | 6.9
| MKK | 76.9 | 21.2 | 1.9
| TSI | 77.2 | 20.8 | 2.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23933737
  |Trait=Myopia (severe)
  |Title=Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia.
  |RiskAllele=T
  |Pval=6E-10
  |OR=1.26
  |ORtxt=[NR]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}