Gene entry
MPO
myeloperoxidase
- Chromosome
- 17
- Cytoband
- 17q22
- Variants (rsID)
- 22
MPO is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q22). Its official name is “myeloperoxidase”. The reference table lists 22 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs28730837Conflicting interpretationssingle nucleotide variantMyeloperoxidase deficiency
- rs119468010Pathogenicsingle nucleotide variantMyeloperoxidase deficiency
- rs119469014Pathogenicsingle nucleotide variantMyeloperoxidase deficiency
- rs536522394PathogenicDeletionMyeloperoxidase deficiency
- rs78950939Pathogenicsingle nucleotide variantMyeloperoxidase deficiency
- rs56378716Uncertain significancesingle nucleotide variantMyeloperoxidase 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.