Gene entry
MYRF
myelin regulatory factor
- Chromosome
- 11
- Cytoband
- 11q12.2
- Variants (rsID)
- 17
MYRF is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q12.2). Its official name is “myelin regulatory factor”. The reference table lists 17 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs174535Not classifiedsynonymous_variantColorectal Adenoma|Colorectal Cancer|Adenoma|Fetal Akinesia Deformation Sequence 2|Fetal Akinesia Deformation Sequence 3
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.