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Gene entry

DNAI1

dynein axonemal intermediate chain 1

Chromosome
9
Cytoband
9p13.3
Variants (rsID)
27

DNAI1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9p13.3). Its official name is “dynein axonemal intermediate chain 1”. The reference table lists 27 variants (rsID) for this gene.

Clinically classified variants

15 reference-table entries with clinical significance.

  • rs16931555Benignsingle nucleotide variantPrimary ciliary dyskinesia|Kartagener syndrome
  • rs202213517Benignsingle nucleotide variantPrimary ciliary dyskinesia|Kartagener syndrome
  • rs76334696Benignsingle nucleotide variantPrimary ciliary dyskinesia
  • rs78865254Benignsingle nucleotide variantPrimary ciliary dyskinesia|Kartagener syndrome
  • rs116938457Conflicting interpretationssingle nucleotide variantPrimary ciliary dyskinesia|Kartagener syndrome
  • rs146434058Conflicting interpretationssingle nucleotide variantPrimary ciliary dyskinesia|Kartagener syndrome
  • rs148701985Conflicting interpretationssingle nucleotide variantPrimary ciliary dyskinesia
  • rs200411544Conflicting interpretationsDeletionPrimary ciliary dyskinesia
  • rs368248592Conflicting interpretationssingle nucleotide variantPrimary ciliary dyskinesia|Kartagener syndrome
  • rs77344166Conflicting interpretationssingle nucleotide variantPrimary ciliary dyskinesia
  • rs200669099Pathogenicsingle nucleotide variantPrimary ciliary dyskinesia|Kartagener syndrome
  • rs769284314Pathogenicsingle nucleotide variantPrimary ciliary dyskinesia
  • rs79833450Pathogenicsingle nucleotide variantKartagener syndrome|Primary ciliary dyskinesia
  • rs138460682Uncertain significancesingle nucleotide variantPrimary ciliary dyskinesia
  • rs140820295Uncertain significancesingle nucleotide variantPrimary ciliary dyskinesia|Kartagener syndrome|Infertility|Male infertility

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.