Gene entry
CETP
cholesteryl ester transfer protein
- Chromosome
- 16
- Cytoband
- 16q13
- Variants (rsID)
- 31
CETP is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q13). Its official name is “cholesteryl ester transfer protein”. The reference table lists 31 variants (rsID) for this gene.
Clinically classified variants
9 reference-table entries with clinical significance.
- rs183130Associationsingle nucleotide variantHigh density lipoprotein cholesterol level quantitative trait locus 10
- rs1532625Benignsingle nucleotide variantHyperalphalipoproteinemia 1
- rs1800777Benignsingle nucleotide variantHyperalphalipoproteinemia 1
- rs1801706Benignsingle nucleotide variantHyperalphalipoproteinemia 1
- rs5880Benignsingle nucleotide variantHyperalphalipoproteinemia 1
- rs5882Benignsingle nucleotide variantHigh density lipoprotein cholesterol level quantitative trait locus 10|Hyperalphalipoproteinemia 1|Coronary artery disorder
- rs5883Benignsingle nucleotide variantHyperalphalipoproteinemia 1
- rs2303790Conflicting interpretationssingle nucleotide variantHyperalphalipoproteinemia 1
- rs5742907Pathogenicsingle nucleotide variantHyperalphalipoproteinemia 1
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.
