{{Rsnum
|rsid=4783961
|Gene=CETP
|Chromosome=16
|position=56960982
|Orientation=plus
|GMAF=0.4063
|Gene_s=CETP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 28.3 | 45.1 | 26.5
| HCB | 6.6 | 31.4 | 62.0
| JPT | 7.1 | 43.4 | 49.6
| YRI | 17.0 | 47.6 | 35.4
| ASW | 10.5 | 59.6 | 29.8
| CHB | 6.6 | 31.4 | 62.0
| CHD | 1.8 | 33.9 | 64.2
| GIH | 40.6 | 42.6 | 16.8
| LWK | 18.2 | 55.5 | 26.4
| MEX | 20.7 | 51.7 | 27.6
| MKK | 17.3 | 50.0 | 32.7
| TSI | 27.5 | 44.1 | 28.4
| HapMapRevision=28
}}{{PMID Auto
|PMID=22143414
|Title=Genetic variation in cholesterol ester transfer protein, serum CETP activity, and coronary artery disease risk in Asian Indian diabetic cohort
|OA=1
}}

{{PMID|18549840|OA=1
}} Cholesterol ester transfer protein, interleukin-8, peroxisome proliferator activator receptor alpha, and Toll-like receptor 4 genetic variations and risk of incident nonfatal myocardial infarction and ischemic stroke.

{{PMID|18637884|OA=1
}} Cholesteryl ester transfer protein (CETP) genetic variation and early onset of non-fatal myocardial infarction.

{{PMID|19041386|OA=1
}} Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}