{{Rsnum
|rsid=2303790
|Gene=CETP
|Chromosome=16
|position=56983380
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.006428
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=CETP
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 100.0 | 0.0 | 0.0
| HCB | 97.0 | 3.0 | 0.0
| JPT | 92.9 | 7.1 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 97.0 | 3.0 | 0.0
| CHD | 96.3 | 3.7 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|desc=CHOLESTEROL ESTER TRANSFER PROTEIN DEFICIENCY
|id=118470
|rsnum=2303790
|variant=0002
}}

{{ClinVar
|rsid=2303790
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=57017292
|CHROM=16
|GMAF=0.0064
|dbSNPBuildID=100
|SSR=0
|SAO=1
|VP=0x050368000000050517110100
|GENEINFO=CETP:1071
|GENE_NAME=CETP
|GENE_ID=1071
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.57017292A>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;PMC;S3D;SLO;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9936; 0.006428
|CLNACC=RCV000032602.22
|CLNDBN=Hyperalphalipoproteinemia
|CLNDSDB=MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C0342883:143470:238080004
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=118470.0002
|COMMON=1
|Disease=Hyperalphalipoproteinemia
}}
[[CETP]] D442G

{{PMID|18560005}} Association of cholesteryl ester transfer protein genotypes with CETP mass and activity, lipid levels, and coronary risk.

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

{{PMID|19131662|OA=1
}} A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.

{{PMID|19682379|OA=1
}} TagSNP transferability and relative loss of variability prediction from HapMap to an admixed population.

{{GET Evidence
|gene=CETP
|aa_change=Asp459Gly
|aa_change_short=D459G
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2303790
|overall_frequency_n=3
|overall_frequency_d=10758
|overall_frequency=0.000278862
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|pph2_score=0.614
|genetests_testable=Y
|nblosum100=4
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}