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Gene entry

MYO3A

myosin IIIA

Chromosome
10
Cytoband
10p12.1
Variants (rsID)
67

MYO3A is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10p12.1). Its official name is “myosin IIIA”. The reference table lists 67 variants (rsID) for this gene.

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Clinically classified variants

37 reference-table entries with clinical significance.

  • rs1999240Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs33947968Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs33968748Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs34204285Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs34615182Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs34918608Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs35010955Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs3740232Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs3758449Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs3824700Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs112195128Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs114982270Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs138955440Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs139958275Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs140301218Conflicting interpretationssingle nucleotide variant
  • rs143918373Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs146511800Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30|Hearing impairment
  • rs146647767Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs146693681Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs146832858Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs147376000Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs147749053Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs35447806Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs35575696Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs35675577Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs371741845Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs372169216Conflicting interpretationssingle nucleotide variant
  • rs3737274Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs375346333Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs375717548Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs56147819Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs61729833Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs61731629Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs72787346Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs199541460Uncertain significancesingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30
  • rs201323717Uncertain significancesingle nucleotide variant
  • rs72787376Uncertain significancesingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 30

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.