Gene entry
MYO1A
myosin IA
- Chromosome
- 12
- Cytoband
- 12q13.3
- Variants (rsID)
- 24
MYO1A is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12q13.3). Its official name is “myosin IA”. The reference table lists 24 variants (rsID) for this gene.
Clinically classified variants
15 reference-table entries with clinical significance.
- rs141658242Benignsingle nucleotide variant
- rs150587673Benignsingle nucleotide variant
- rs151269703Benignsingle nucleotide variant
- rs33962952Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 48
- rs55679042Benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 48
- rs121909305Conflicting interpretationssingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 48
- rs148582008Conflicting interpretationssingle nucleotide variant
- rs370708976Conflicting interpretationssingle nucleotide variant
- rs55985817Conflicting interpretationssingle nucleotide variant
- rs138855953Likely benignsingle nucleotide variant
- rs143613424Likely benignsingle nucleotide variant
- rs151187460Likely benignsingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 48
- rs369452147Likely benignsingle nucleotide variant
- rs77915386Likely benignsingle nucleotide variant
- rs61753849Uncertain significancesingle nucleotide variantAutosomal dominant nonsyndromic hearing loss 48
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.