Gene entry
HP
haptoglobin
- Chromosome
- 16
- Cytoband
- 16q22.2
- Variants (rsID)
- 5
HP is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q22.2). Its official name is “haptoglobin”. The reference table lists 5 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs104894517Othersingle nucleotide variantAnhaptoglobinemia
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.
