Gene entry
MYO1C
myosin IC
- Chromosome
- 17
- Cytoband
- 17p13.3
- Variants (rsID)
- 19
MYO1C is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17p13.3). Its official name is “myosin IC”. The reference table lists 19 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs11538161Benignsingle nucleotide variant
- rs2286873Benignsingle nucleotide variant
- rs2286877Benignsingle nucleotide variant
- rs61753652Benignsingle nucleotide variant
- rs77445493Benignsingle nucleotide variant
- rs117696188Likely benignsingle nucleotide variant
- rs45598333Likely benignsingle 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.