SNP information rs651821

Research and publications:

  17357073   Genetic analysis of 103 candidate genes for coronary artery disease and associated phenotypes in a founder population reveals a new association between endothelin-1 and high-density lipoprotein cholesterol

  17357083   Medical sequencing at the extremes of human body mass.

  18078817   Multiple genetic determinants of plasma lipid levels in Caribbean Hispanics.

  18196181   Correction of population stratification in large multi-ethnic association studies

  18441017   An apolipoprotein A-V gene SNP is associated with marked hypertriglyceridemia among Asian-American patients.

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

  19299407   Replication of genetic associations with plasma lipoprotein traits in a multiethnic sample

  19732897   Associations of polymorphisms in the apolipoprotein A1/C3/A4/A5 gene cluster with familial combined hyperlipidaemia in Hong Kong Chinese.

  19913121   Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip

  20054229   Gene-gene interaction between APOA5 and USF1: two candidate genes for the metabolic syndrome.

  20335584   Apolipoprotein C3 gene variants in nonalcoholic fatty liver disease

  20395964   Different effects of apolipoprotein A5 SNPs and haplotypes on triglyceride concentration in three ethnic origins.

  20452521   Triglyceride-mediated pathways and coronary disease: collaborative analysis of 101 studies.

  20570915   Genetic determinants of major blood lipids in Pakistanis compared with Europeans.

  21375366   Impact of apolipoprotein A5 (APOA5) polymorphisms on serum triglyceride levels in schizophrenic patients under long-term atypical antipsychotic treatment.

  21527746   Triglycerides and heart disease: still a hypothesis?

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

  21880794   Hyperlipoproteinemia type 1 and recurrent acute pancreatitis caused by antibodies to lipoprotein lipase in a young girl with Sjögren's syndrome.

  21889769   Variants in the APOA5 gene region and the response to combination therapy with statins and fenofibric acid in a randomized clinical trial of individuals with mixed dyslipidemia.

  22171074   A genome-wide association and gene-environment interaction study for serum triglycerides levels in a healthy Chinese male population.

  22425169   Vitamin D dependent effects of APOA5 polymorphisms on HDL cholesterol.

  22460246   Influence of genetic variants in the apolipoprotein A5 and C3 gene on lipids, lipoproteins, and its association with coronary artery disease in Indians.

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

  24178511   Gene-centric association signals for haemostasis and thrombosis traits identified with the HumanCVD BeadChip.

  24725463   Analysis of common and coding variants with cardiovascular disease in the Diabetes Heart Study.

  24903888   Triglyceride-raising APOA5 genetic variants are associated with obesity and non-HDL-C in Chinese children and adolescents.

  24918908   Genomic and metabolomic profile associated to microalbuminuria.

  26345861   Relationship of the APOA5/A4/C3/A1 gene cluster and APOB gene polymorphisms with dyslipidemia.

  26397108   Effects of Polymorphisms in APOA4-APOA5-ZNF259-BUD13 Gene Cluster on Plasma Levels of Triglycerides and Risk of Coronary Heart Disease in a Chinese Han Population.

  26634697   Multiple susceptibility loci at chromosome 11q23.3 are associated with plasma triglyceride in East Asians.

  26690388   Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese.

  26824674   Interactions of Environmental Factors and APOA1-APOC3-APOA4-APOA5 Gene Cluster Gene Polymorphisms with Metabolic Syndrome.

  27257688   Distinct Patterns of Association of Variants at 11q23.3 Chromosomal Region with Coronary Artery Disease and Dyslipidemia in the Population of Andhra Pradesh, India.

  28067407   Analysis of Whole Exome Sequencing with Cardiometabolic Traits Using Family-Based Linkage and Association in the IRAS Family Study.

  28099408   Multiphenotype association study of patients randomized to initiate antiretroviral regimens in AIDS Clinical Trials Group protocol A5202.

  28371326   Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study.

  28624160   Association of apolipoprotein A5 gene variants with metabolic syndrome in Tunisian population.

  28947988   Association analysis of APO gene polymorphisms with ischemic stroke risk: a case-control study in a Chinese Han population.

  29618726   Exome Sequencing Identifies Genetic Variants Associated with Circulating Lipid Levels in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study (IRASFS).

  29866721   Effects of polymorphisms in APOA5 on the plasma levels of triglycerides and risk of coronary heart disease in Jilin, northeast China: a case-control study.

  30631647   Functional polymorphisms of the APOA1/C3/A4/A5-ZPR1-BUD13 gene cluster are associated with dyslipidemia in a sex-specific pattern.

  30740535   Coronary artery disease, genetic risk and the metabolome in young individuals.

  30929539   APOA5 rs651821 confers increased risk for hypertension in Tongdao Dong population.

  31165758   Association of BUD13-ZNF259-APOA5-APOA1-SIK3 cluster polymorphism in 11q23.3 and structure of APOA5 with increased plasma triglyceride levels in a Korean population.

  31181149   Interaction of polymorphisms in APOA4-APOA5-ZPR1-BUD13 gene cluster and sleep duration on 5-year lipid changes in middle aged and older Chinese.

  32725151   Association of rs662799 variant and APOA5 gene haplotypes with metabolic syndrome and its components: a meta-analysis in North Africa.

  33986338   Kernel machine SNP set analysis finds the association of BUD13, ZPR1, and APOA5 variants with metabolic syndrome in Tehran Cardio-metabolic Genetics Study.

  34159422   Host genetic control of gut microbiome composition.