CETP, cholesteryl ester transfer protein, 1071

N. diseases: 188; N. variants: 88
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1567476573
rs1567476573
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C3149462
Disease:
HYPERALPHALIPOPROTEINEMIA 1
GT 0.700 CausalMutation CLINVAR
dbSNP: rs5742907
rs5742907
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C3149462
Disease:
HYPERALPHALIPOPROTEINEMIA 1
A 0.700 CausalMutation CLINVAR
dbSNP: rs708272
rs708272
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0154251
Disease:
Lipid Metabolism Disorders
0.010 GeneticVariation BEFREE <b>:</b> The <i>TaqI</i> B (rs708272) single-nucleotide variant, i.e., the +279 G/A substitution in intron 1 of the <i>CETP</i> gene, is actively investigated as a risk factor of lipid metabolism disorders. 31739638 2019
dbSNP: rs711752
rs711752
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0524620
Disease:
Metabolic Syndrome X
0.010 GeneticVariation BEFREE (2) rs1800775, rs3764261, rs12149545, rs711752, and rs708272 polymorphisms were significantly related to the risk of MS (all <i>p</i> < 0.05). 28629169 2017
dbSNP: rs708272
rs708272
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0524620
Disease:
Metabolic Syndrome X
0.030 GeneticVariation BEFREE (2) rs1800775, rs3764261, rs12149545, rs711752, and rs708272 polymorphisms were significantly related to the risk of MS (all <i>p</i> < 0.05). 28629169 2017
dbSNP: rs1800775
rs1800775
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0524620
Disease:
Metabolic Syndrome X
0.020 GeneticVariation BEFREE (3) The rs1800775 polymorphism was associated with high fasting blood glucose levels and low high density lipoprotein cholesterol (HDL-C); rs3764261 and rs12149545 polymorphisms were associated with all components of MS except high blood pressure; rs711752 and rs708272 polymorphisms were associated with low HDL-C (all <i>p</i> < 0.05). 28629169 2017
dbSNP: rs1800775
rs1800775
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE (3) The rs1800775 polymorphism was associated with high fasting blood glucose levels and low high density lipoprotein cholesterol (HDL-C); rs3764261 and rs12149545 polymorphisms were associated with all components of MS except high blood pressure; rs711752 and rs708272 polymorphisms were associated with low HDL-C (all <i>p</i> < 0.05). 28629169 2017
dbSNP: rs711752
rs711752
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE (3) The rs1800775 polymorphism was associated with high fasting blood glucose levels and low high density lipoprotein cholesterol (HDL-C); rs3764261 and rs12149545 polymorphisms were associated with all components of MS except high blood pressure; rs711752 and rs708272 polymorphisms were associated with low HDL-C (all <i>p</i> < 0.05). 28629169 2017
dbSNP: rs708272
rs708272
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE (3) The rs1800775 polymorphism was associated with high fasting blood glucose levels and low high density lipoprotein cholesterol (HDL-C); rs3764261 and rs12149545 polymorphisms were associated with all components of MS except high blood pressure; rs711752 and rs708272 polymorphisms were associated with low HDL-C (all <i>p</i> < 0.05). 28629169 2017
dbSNP: rs5882
rs5882
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0577631
Disease:
Carotid Atherosclerosis
0.020 GeneticVariation BEFREE I405V and Taq1B polymorphisms were not associated with the risk of carotid atherosclerosis and longevity. 24468472 2014
dbSNP: rs9939224
rs9939224
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0524620
Disease:
Metabolic Syndrome X
G 0.800 GeneticVariation GWASDB A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085 2011
dbSNP: rs9939224
rs9939224
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0524620
Disease:
Metabolic Syndrome X
G 0.800 GeneticVariation GWASCAT A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085 2011
dbSNP: rs5882
rs5882
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0007222
Disease:
Cardiovascular Diseases
0.030 GeneticVariation BEFREE A cholesteryl ester transfer protein (CETP) genotype (V/V homozygosity for I405V, NCBI dbSNP rs5882) has been associated with preservation of cognitive function in old age, in addition to its associations with exceptional longevity and cardiovascular disease. 17531380 2007
dbSNP: rs1800775
rs1800775
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0392885
Disease:
High density lipoprotein measurement
A 0.800 GeneticVariation GWASCAT A common variant association study reveals novel susceptibility loci for low HDL-cholesterol levels in ethnic Arabs. 26879886 2016
dbSNP: rs11076174
rs11076174
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0392885
Disease:
High density lipoprotein measurement
T 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs118146573
rs118146573
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C1445957
Disease:
Serum total cholesterol measurement
G 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs12720922
rs12720922
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C1445957
Disease:
Serum total cholesterol measurement
G 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs12720922
rs12720922
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0392885
Disease:
High density lipoprotein measurement
G 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs17231506
rs17231506
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0392885
Disease:
High density lipoprotein measurement
C 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs17231506
rs17231506
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0202236
Disease:
Triglycerides measurement
C 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs17231506
rs17231506
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C1445957
Disease:
Serum total cholesterol measurement
C 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs17231520
rs17231520
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0392885
Disease:
High density lipoprotein measurement
G 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs289742
rs289742
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0392885
Disease:
High density lipoprotein measurement
C 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs5880
rs5880
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0392885
Disease:
High density lipoprotein measurement
G 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs5883
rs5883
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0392885
Disease:
High density lipoprotein measurement
C 0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018