Gene entry
MAG
myelin associated glycoprotein
- Chromosome
- 19
- Cytoband
- 19q13.12
- Variants (rsID)
- 11
MAG is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19q13.12). Its official name is “myelin associated glycoprotein”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs144553163Conflicting interpretationssingle nucleotide variantHereditary spastic paraplegia|Hereditary spastic paraplegia 75
- rs142375870Uncertain significancesingle nucleotide variantHereditary spastic paraplegia|Hereditary spastic paraplegia 75
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.