Gene entry
APOC2
apolipoprotein C2
- Chromosome
- 19
- Cytoband
- 19q13.32
- Variants (rsID)
- 3
APOC2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19q13.32). Its official name is “apolipoprotein C2”. The reference table lists 3 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs5126Benignsingle nucleotide variantAPOLIPOPROTEIN C-II (AFRICAN)|Familial apolipoprotein C-II 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.