Gene entry
MAGEL2
MAGE family member L2
- Chromosome
- 15
- Cytoband
- 15q11.2
- Variants (rsID)
- 3
MAGEL2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q11.2). Its official name is “MAGE family member L2”. The reference table lists 3 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs115892604Benignsingle 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.
