Gene entry
MAB21L2
mab-21 like 2
- Chromosome
- 4
- Cytoband
- 4q31.3
- Variants (rsID)
- 4
MAB21L2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 4 (region 4q31.3). Its official name is “mab-21 like 2”. The reference table lists 4 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs587777511Likely pathogenicsingle nucleotide variantColobomatous microphthalmia-rhizomelic dysplasia syndrome
- rs587777512Likely pathogenicsingle nucleotide variantColobomatous microphthalmia-rhizomelic dysplasia syndrome
- rs587777513Likely pathogenicsingle nucleotide variantColobomatous microphthalmia-rhizomelic dysplasia syndrome
- rs587777514Likely pathogenicsingle nucleotide variantColobomatous microphthalmia-rhizomelic dysplasia syndrome
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
