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Gene entry

MYH14

myosin heavy chain 14

Chromosome
19
Cytoband
19q13.33
Variants (rsID)
70

MYH14 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19q13.33). Its official name is “myosin heavy chain 14”. The reference table lists 70 variants (rsID) for this gene.

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Clinically classified variants

21 reference-table entries with clinical significance.

  • rs115019972Benignsingle nucleotide variant
  • rs11666328Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 4A|Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome
  • rs11669191Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 4A
  • rs140118363Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 4A
  • rs147447646Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 4A
  • rs199915414Benignsingle nucleotide variant
  • rs34773557Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 4A
  • rs3745504Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 4A|Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome
  • rs55645295Benignsingle nucleotide variant
  • rs627491Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 4A
  • rs75915336Benignsingle nucleotide variant
  • rs119103280Conflicting interpretationssingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 4A
  • rs142696359Conflicting interpretationssingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 4A
  • rs200818171Conflicting interpretationssingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 4A
  • rs201337011Conflicting interpretationssingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 4A|Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome
  • rs368124508Conflicting interpretationssingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 4A
  • rs561531825Conflicting interpretationssingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 4A
  • rs190941610Likely benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 4A
  • rs113993956Pathogenicsingle nucleotide variantPeripheral neuropathy-myopathy-hoarseness-hearing loss syndrome
  • rs119103281Pathogenicsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 4A
  • rs187782753Uncertain significancesingle nucleotide variant

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.