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Gene entry

MYO15A

myosin XVA

Chromosome
17
Cytoband
17p11.2
Variants (rsID)
59

MYO15A is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17p11.2). Its official name is “myosin XVA”. The reference table lists 59 variants (rsID) for this gene.

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Clinically classified variants

40 reference-table entries with clinical significance.

  • rs114328138Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs115393178Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs16960961Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs2272571Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs2280777Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs8077577Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs854800Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs1006770Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs117612144Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs121908970Conflicting interpretationssingle nucleotide variantDeafness, with smith-magenis syndrome|Autosomal recessive nonsyndromic hearing loss 3
  • rs138861831Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3|Childhood onset hearing loss
  • rs140140417Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs141183007Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs141475629Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs143316414Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs144909486Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs147458358Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs148723625Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs181355572Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs183256997Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs185688918Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs186426892Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs199621031Conflicting interpretationssingle nucleotide variantRare genetic deafness|Autosomal recessive nonsyndromic hearing loss 3
  • rs200146361Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs200456053Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs200583193Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs200623501Conflicting interpretationssingle nucleotide variant
  • rs201487604Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs201689819Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs201734915Conflicting interpretationssingle nucleotide variant
  • rs201737186Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs368755362Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs370047914Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs376351191Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs55688805Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs558947304Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs59933498Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 3
  • rs184435771Pathogenicsingle nucleotide variantRare genetic deafness|Inborn genetic diseases|Autosomal recessive nonsyndromic hearing loss 3|Hearing impairment
  • rs201978571Pathogenicsingle nucleotide variantRare genetic deafness|Autosomal recessive nonsyndromic hearing loss 3
  • rs377015931Pathogenicsingle nucleotide variantRare genetic deafness|Autosomal recessive nonsyndromic hearing loss 3

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.