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Gene entry

ZEB2

zinc finger E-box binding homeobox 2

Chromosome
2
Cytoband
2q22.3
Variants (rsID)
47

ZEB2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2q22.3). Its official name is “zinc finger E-box binding homeobox 2”. The reference table lists 47 variants (rsID) for this gene.

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Clinically classified variants

19 reference-table entries with clinical significance.

  • rs112005830Benignsingle nucleotide variantMowat-Wilson syndrome|History of neurodevelopmental disorder
  • rs140593583Benignsingle nucleotide variantMowat-Wilson syndrome
  • rs143854197Benignsingle nucleotide variantMowat-Wilson syndrome|History of neurodevelopmental disorder
  • rs145812868Benignsingle nucleotide variantHistory of neurodevelopmental disorder|Mowat-Wilson syndrome
  • rs199951665Benignsingle nucleotide variantMowat-Wilson syndrome|History of neurodevelopmental disorder
  • rs201180901Benignsingle nucleotide variantMowat-Wilson syndrome
  • rs201881288Benignsingle nucleotide variantMowat-Wilson syndrome|History of neurodevelopmental disorder
  • rs34890427Benignsingle nucleotide variantMowat-Wilson syndrome|History of neurodevelopmental disorder
  • rs369622877Benignsingle nucleotide variantMowat-Wilson syndrome
  • rs372940559Benignsingle nucleotide variantMowat-Wilson syndrome
  • rs6711223Benignsingle nucleotide variantMowat-Wilson syndrome|History of neurodevelopmental disorder
  • rs767506087Benignsingle nucleotide variantMowat-Wilson syndrome
  • rs149882004Conflicting interpretationssingle nucleotide variantMowat-Wilson syndrome|History of neurodevelopmental disorder
  • rs185223937Conflicting interpretationssingle nucleotide variantHistory of neurodevelopmental disorder|Mowat-Wilson syndrome
  • rs754532627Conflicting interpretationssingle nucleotide variantMowat-Wilson syndrome
  • rs149035844Likely benignsingle nucleotide variantMowat-Wilson syndrome
  • rs137852981Pathogenicsingle nucleotide variantMowat-Wilson syndrome
  • rs786204813PathogenicDeletionMowat-Wilson syndrome
  • rs886041338Pathogenicsingle nucleotide variantMowat-Wilson syndrome

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.