SNP information rs2048327

Research and publications:

  19591196   Expression of organic cation transporters OCT1 (SLC22A1) and OCT3 (SLC22A3) is affected by genetic factors and cholestasis in human liver.

  19956433   Genetics of coronary artery disease: focus on genome-wide association studies.

  20429798   Association of the SLC22A1, SLC22A2, and SLC22A3 genes encoding organic cation transporters with diabetic nephropathy and hypertension.

  20601648   Lipoprotein(a) levels and long-term cardiovascular risk in the contemporary era of statin therapy.

  20729558   Improved prediction of cardiovascular disease based on a panel of single nucleotide polymorphisms identified through genome-wide association studies.

  21242481   Genetic risk score and risk of myocardial infarction in Hispanics.

  21369780   Genome-wide association studies in atherosclerosis.

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

  21900290   Genetic variants, plasma lipoprotein(a) levels, and risk of cardiovascular morbidity and mortality among two prospective cohorts of type 2 diabetes.

  22084709   Evaluation of genetic variations in organic cationic transporter 3 in depressed and nondepressed subjects.

  22152955   Genetic susceptibility to coronary heart disease in type 2 diabetes: 3 independent studies.

  22216278   Large scale association analysis identifies three susceptibility loci for coronary artery disease.

  22848412   Genetic markers enhance coronary risk prediction in men: the MORGAM prospective cohorts.

  22882272   Genetic variants associated with myocardial infarction in the PSMA6 gene and Chr9p21 are also associated with ischaemic stroke.

  23036009   Lack of association between four SNPs in the SLC22A3-LPAL2-LPA gene cluster and coronary artery disease in a Chinese Han population: a case control study.

  24219970   Common genetic variants do not associate with CAD in familial hypercholesterolemia.

  26847647   Experimental Biology for the Identification of Causal Pathways in Atherosclerosis.

  26892960   From Loci to Biology: Functional Genomics of Genome-Wide Association for Coronary Disease.

  26896185   Human Genetics and the Causal Role of Lipoprotein(a) for Various Diseases.

  26934567   Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.

  26950853   Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium.

  27621937   A Case-Control Study of the Relationship Between SLC22A3-LPAL2-LPA Gene Cluster Polymorphism and Coronary Artery Disease in the Han Chinese Population.

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

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

  30772277   SLC22A3 is associated with lipoprotein (a) concentration and cardiovascular disease in familial hypercholesterolemia.

  32685059   Association Study of Coronary Artery Disease-Associated Genome-Wide Significant SNPs with Coronary Stenosis in Pakistani Population.

  33581269   Low HDL concentration in rs2048327-G carriers can predispose men to develop coronary heart disease: Tehran Cardiometabolic genetic study (TCGS).

  34969749   A Single Nucleotide Polymorphism (SNP) in the SLC22A3 Transporter Gene Is Associated With the Severity of Oral Mucositis in Multiple Myeloma Patients Receiving Autologous Stem Cell Transplant Followed by Melphalan Therapy.