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SNP information rs1800775

RS1800775

Normal allele: AA

Polymorphism rs1800775 is related to topics like this:

Factor 5 blood clotting disorder

Thrombophilia, an increased tendency to form abnormal blood clots that can obstruct blood vessels,...


Research and publications:

  12434007   SNP genotyping on a genome-wide amplified DOP-PCR template.

  12475937   Association testing by DNA pooling: an effective initial screen.

  17903299   A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study

  18193044   Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.

  18513389   New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background

  18549840   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.

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

  18637884   Cholesteryl ester transfer protein (CETP) genetic variation and early onset of non-fatal myocardial infarction.

  19041386   Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.

  19060910   Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

  19131662   A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients

  19197348   Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae

  19263529   Genetic risk factors in recurrent venous thromboembolism: A multilocus, population-based, prospective approach

  19429595   Genome-wide linkage scan for plasma high density lipoprotein cholesterol, apolipoprotein A-1 and triglyceride variation among American Indian populations: the Strong Heart Family Study.

  19435741   Common lipid-altering gene variants are associated with therapeutic intervention thresholds of lipid levels in older people.

  19729614   Ion mobility analysis of lipoprotein subfractions identifies three independent axes of cardiovascular risk.

  19773416   A gene score of nine LDL and HDL regulating genes is associated with fluvastatin-induced cholesterol changes in women.

  19951432   Analysis of recently identified dyslipidemia alleles reveals two loci that contribute to risk for carotid artery disease

  20018036   Using a latent growth curve model for an integrative assessment of the effects of genetic and environmental factors on multiple phenotypes.

  20031591   Association of blood lipids with common DNA sequence variants at 19 genetic loci in the multiethnic United States National Health and Nutrition Examination Survey III.

  20205905   Association of repeatedly measured intermediate risk factors for complex diseases with high dimensional SNP data.

  20370913   Genome-wide association analysis of total cholesterol and high-density lipoprotein cholesterol levels using the Framingham heart study data.

  20421590   Genetic causes of high and low serum HDL-cholesterol.

  21103364   Multi-locus test conditional on confirmed effects leads to increased power in genome-wide association studies.

  21118897   Increased power of mixed models facilitates association mapping of 10 loci for metabolic traits in an isolated population.

  21292264   Genetic predisposition influences plasma lipids of participants on habitual diet, but not the response to reductions in dietary intake of saturated fatty acids.

  21407270   Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration.

  21424820   Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration.

  21467728   Profile of participants and genotype distributions of 108 polymorphisms in a cross-sectional study of associations of genotypes with lifestyle and clinical factors: a project in the Japan Multi-Institutional Collaborative Cohort (J-MICC) Study.

  21589926   Knowledge-driven multi-locus analysis reveals gene-gene interactions influencing HDL cholesterol level in two independent EMR-linked biobanks.

  21686126   An assessment of CETP sequence variation in relation to cognitive decline and dementia risk.

  21708280   Candidate gene studies in gallbladder cancer: a systematic review and meta-analysis

  21738485   Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study.

  21860704   Implications of discoveries from genome-wide association studies in current cardiovascular practice.

  22229114   Common Variants in 6 Lipid-Related Genes Discovered by High-Resolution DNA Melting Analysis and Their Association with Plasma Lipids.

  22715478   Genotypes associated with lipid metabolism contribute to differences in serum lipid profile of GH-deficient adults before and after GH replacement therapy.

  22994408   Transferability and fine mapping of genome-wide associated loci for lipids in African Americans.

  23050023   Association of genetic variants influencing lipid levels with coronary artery disease in Japanese individuals.

  23101478   Single nucleotide polymorphisms (SNPs) involved in insulin resistance, weight regulation, lipid metabolism and inflammation in relation to metabolic syndrome: an epidemiological study.

  23497168   Omega-3 fatty acids, polymorphisms and lipid related cardiovascular disease risk factors in the Inuit population.

  23675527   The association of common SNPs and haplotypes in CETP gene with HDL cholesterol levels in Latvian population.

  23696881   Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation.

  24931982   GRASP: analysis of genotype-phenotype results from 1390 genome-wide association studies and corresponding open access database.

  25205864   Genetic determinants of age-related macular degeneration in diverse populations from the PAGE study.

  26365620   Genetic association of APOA5 and APOE with metabolic syndrome and their interaction with health-related behavior in Korean men.

  26694435   Association between Eight Functional Polymorphisms and Haplotypes in the Cholesterol Ester Transfer Protein (CETP) Gene and Dyslipidemia in National Minority Adults in the Far West Region of China.

  26879886   A common variant association study reveals novel susceptibility loci for low HDL-cholesterol levels in ethnic Arabs.

  27545125   [Association between CETP polymorphisms and haplotypes with dyslipidemia in Xinjiang Uygur and Kazak residents].

  27768712   c.*84G>A Mutation in CETP Is Associated with Coronary Artery Disease in South Indians.

  28106113   Genetic risk variants for metabolic traits in Arab populations.

  28209224   Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.

  28577571   Genetic determinants of inherited susceptibility to hypercholesterolemia - a comprehensive literature review.

  28629169   Association between Six CETP Polymorphisms and Metabolic Syndrome in Uyghur Adults from Xinjiang, China.

  28652652   Gallbladder cancer epidemiology, pathogenesis and molecular genetics: Recent update.

  28666712   The association between six genetic variants and blood lipid levels in pregnant Chinese Han women.

  28918250   Associations of cholesteryl ester transfer protein (CETP) gene variants with predisposition to age-related macular degeneration.

  29080057   Sex Differences in Blood HDL-c, the Total Cholesterol/HDL-c Ratio, and Palmitoleic Acid are Not Associated with Variants in Common Candidate Genes.

  29525920   Lack of association between FTO gene variations and metabolic healthy obese (MHO) phenotype: Tehran Cardio-metabolic Genetic Study (TCGS).

  29695241   Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes.

  30108155   Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population.

  31108953   Genetic and Non-Genetic Factor-Adjusted Association between Coffee Drinking and High-Density Lipoprotein Cholesterol in Taiwanese Adults: Stratification by Sex.

  31366177   Genome-Wide Association Study of Metabolic Syndrome Reveals Primary Genetic Variants at CETP Locus in Indians.

  31597401   Cholesteryl Ester Transfer Protein Genetic Variants Associated with Risk for Type 2 Diabetes and Diabetic Kidney Disease in Taiwanese Population.

  32551884   Association of the -629C>A (rs1800775) CETP Polymorphism with the Development of Essential Hypertension in Mexican Population.

  32666702   Association of genetic variants at CETP, AGER, and CYP4F2 locus with the risk of atrophic age-related macular degeneration.

  35387194   Personalized Dietary Recommendations Based on Lipid-Related Genetic Variants: A Systematic Review.

  20031564   CETP gene polymorphisms, HDL cholesterol, and risk of future myocardial infarction: a genome-wide analysis among 18,245 initially healthy women in the Women's Genome Health Study.

  22122979   The CETP I405V polymorphism is associated with an increased risk of Alzheimer's disease.

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