Gene entry
MYF6
myogenic factor 6
- Chromosome
- 12
- Cytoband
- 12q21.31
- Variants (rsID)
- 7
MYF6 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12q21.31). Its official name is “myogenic factor 6”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs138296448Benignsingle nucleotide variantMyopathy, centronuclear, 3|Autosomal dominant centronuclear myopathy
- rs1047183Likely benignsingle nucleotide variantCentronuclear Myopathy, Dominant
- rs141278987Likely benignsingle nucleotide variantMyopathy, centronuclear, 3
- rs143677057Uncertain significancesingle nucleotide variantMyopathy, centronuclear, 3
- rs190471225Uncertain significancesingle nucleotide variantMyopathy, centronuclear, 3
- rs28928909Uncertain significancesingle nucleotide variantMyopathy, centronuclear, 3|Autosomal dominant centronuclear myopathy
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.