SNP information rs867186

Research and publications:

  16846490   Lemierre's syndrome and genetic polymorphisms: case report

  18680534   PROC, PROCR and PROS1 polymorphisms, plasma anticoagulant phenotypes, and risk of cardiovascular disease and mortality in older adults: the Cardiovascular Health Study.

  18947391   Hemostasis and ageing.

  20231535   Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium.

  20802025   Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study.

  21637794   Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue.

  21676895   A gene-centric association scan for Coagulation Factor VII levels in European and African Americans: the Candidate Gene Association Resource (CARe) Consortium.

  21857382   Candidate genes and risk for CP: a population-based study.

  21980494   Genetics of venous thrombosis: insights from a new genome wide association study.

  22216198   A genome-wide association study of the Protein C anticoagulant pathway.

  22251481   The endothelial protein C receptor (PROCR) Ser219Gly variant and risk of common thrombotic disorders: a HuGE review and meta-analysis of evidence from observational studies.

  22443383   Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project.

  23136988   Association of soluble endothelial protein C receptor plasma levels and PROCR rs867186 with cardiovascular risk factors and cardiovascular events in coronary artery disease patients: the Athero Gene study.

  24635948   Association of the endothelial protein C receptor (PROCR) rs867186-G allele with protection from severe malaria.

  24744624   The Effects of Endothelial Protein C Receptor Gene Polymorphisms on the Plasma sEPCR Level in Venous Thrombosis Patients.

  24816905   Single nucleotide variants in the protein C pathway and mortality in dialysis patients.

  25376901   Genetic markers associated with plasma protein C level in African Americans: the atherosclerosis risk in communities (ARIC) study.

  25533856   Familial thrombotic risk based on the genetic background of Protein C Deficiency in a Portuguese Study.

  25541704   Endothelial protein C receptor gene variants not associated with severe malaria in ghanaian children.

  25951190   Networks in Coronary Heart Disease Genetics As a Step towards Systems Epidemiology.

  26293461   Prediction of Causal Candidate Genes in Coronary Artery Disease Loci.

  27215212   Association of common genetic variation in the protein C pathway genes with clinical outcomes in acute respiratory distress syndrome.

  27255786   The endothelial protein C receptor rs867186-GG genotype is associated with increased soluble EPCR and could mediate protection against severe malaria.

  27386823   Integrative functional genomics identifies regulatory mechanisms at coronary artery disease loci.

  28415941   Endothelial protein C receptor polymorphisms and risk of sepsis in a Chinese population.

  28530674   Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms.

  28739976   Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.

  29112333   Associations of activated coagulation factor VII and factor VIIa-antithrombin levels with genome-wide polymorphisms and cardiovascular disease risk.

  29190926   Polymorphism of the ABO gene associate with thrombosis risk in patients with paroxysmal nocturnal hemoglobinuria.

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

  30065929   Integrating Genes Affecting Coronary Artery Disease in Functional Networks by Multi-OMICs Approach.

  31420334   Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism.

  31645483   Polymorphisms in endothelial protein C receptor gene and Kawasaki disease susceptibility in a Chinese children.

  32153634   Association of EPCR Polymorphism rs867186-GG With Severity of Human Malaria.

  35021256   Thrombotic Risk Determined by Protein C Receptor (PROCR) Variants among Middle-Aged and Older Adults: A Population-Based Cohort Study.