Gene entry
MBL2
mannose binding lectin 2
- Chromosome
- 10
- Cytoband
- 10q21.1
- Variants (rsID)
- 9
MBL2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q21.1). Its official name is “mannose binding lectin 2”. The reference table lists 9 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs1800451Benignsingle nucleotide variantMannose-binding lectin deficiency
- rs1800450Conflicting interpretationssingle nucleotide variantMannose-binding lectin deficiency
- rs5030737Conflicting interpretationssingle nucleotide variantMannose-binding lectin deficiency|Cystic fibrosis
- rs10824792Likely benignsingle nucleotide variantMannose-binding lectin deficiency
- rs2083771Likely benignsingle nucleotide variantMannose-binding lectin deficiency
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.