Gene entry
MYNN
myoneurin
- Chromosome
- 3
- Cytoband
- 3q26.2
- Variants (rsID)
- 3
MYNN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q26.2). Its official name is “myoneurin”. The reference table lists 3 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs10936599Associationsingle nucleotide variantChronic osteomyelitis
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.