Gene entry
MATN3
matrilin 3
- Chromosome
- 2
- Cytoband
- 2p24.1
- Variants (rsID)
- 9
MATN3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2p24.1). Its official name is “matrilin 3”. The reference table lists 9 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs52826764Benignsingle nucleotide variantMultiple epiphyseal dysplasia type 5|Connective tissue disorder
- rs77245812Benignsingle nucleotide variantOsteoarthritis susceptibility 2|Multiple epiphyseal dysplasia type 5|Connective tissue disorder
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.