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Gene entry

NME8

NME/NM23 family member 8

Chromosome
7
Cytoband
7p14.1
Variants (rsID)
29

NME8 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7p14.1). Its official name is “NME/NM23 family member 8”. The reference table lists 29 variants (rsID) for this gene.

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Clinically classified variants

5 reference-table entries with clinical significance.

  • rs117149381Benignsingle nucleotide variantPrimary ciliary dyskinesia 6
  • rs3213976Benignsingle nucleotide variantPrimary ciliary dyskinesia 6
  • rs62001869Benignsingle nucleotide variantPrimary ciliary dyskinesia 6
  • rs199920317Uncertain significancesingle nucleotide variantPrimary ciliary dyskinesia 6
  • rs201867197Uncertain significancesingle nucleotide variantPrimary ciliary dyskinesia 6

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.