Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Gene entry

COCH

cochlin

Chromosome
14
Cytoband
14q12
Variants (rsID)
17

COCH is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 14 (region 14q12). Its official name is “cochlin”. The reference table lists 17 variants (rsID) for this gene.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Clinically classified variants

9 reference-table entries with clinical significance.

  • rs147841606Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 9|Nonsyndromic genetic hearing loss
  • rs17097458Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 9
  • rs17097468Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 9
  • rs202109231Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 9|Nonsyndromic genetic hearing loss
  • rs2239581Benignsingle nucleotide variant
  • rs28362775Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 9|Nonsyndromic genetic hearing loss
  • rs121908928Pathogenicsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 9
  • rs121908932Pathogenicsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 9|Rare genetic deafness
  • rs28938175Pathogenicsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 9|Nonsyndromic genetic hearing loss|Rare genetic deafness|Hearing impairment

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.