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Gene entry

ZMYND10

zinc finger MYND-type containing 10

Chromosome
3
Cytoband
3p21.31
Variants (rsID)
5

ZMYND10 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p21.31). Its official name is “zinc finger MYND-type containing 10”. The reference table lists 5 variants (rsID) for this gene.

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Clinically classified variants

4 reference-table entries with clinical significance.

  • rs141055331Benignsingle nucleotide variantPrimary ciliary dyskinesia
  • rs142613783Benignsingle nucleotide variantPrimary ciliary dyskinesia
  • rs138815960Pathogenicsingle nucleotide variantPrimary ciliary dyskinesia 22|Kartagener syndrome|Primary ciliary dyskinesia
  • rs200913791Pathogenicsingle nucleotide variantPrimary ciliary dyskinesia 22|Primary ciliary dyskinesia

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.