Gene entry
APOC3
apolipoprotein C3
- Chromosome
- 11
- Cytoband
- 11q23.3
- Variants (rsID)
- 7
APOC3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q23.3). Its official name is “apolipoprotein C3”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs4520Benignsingle nucleotide variantApolipoprotein c-III deficiency
- rs147210663Conflicting interpretationssingle nucleotide variantCoronary heart disease|Apolipoprotein c-III deficiency
- rs76353203Conflicting interpretationssingle nucleotide variantApolipoprotein c-III deficiency|Coronary heart disease
- rs140621530Likely benignsingle nucleotide variantCoronary heart disease|Apolipoprotein c-III 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.