PROCR, protein C receptor, 10544

N. diseases: 110; N. variants: 20
Disease: Deep Vein Thrombosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		0.160 GeneticVariation disease BEFREE We aimed to investigate the relation between EPCR gene polymorphisms (6936A/G and 4678C/G) and deep venous thrombosis (DVT) and their relations to sEPCR level. 26340463 2016
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		0.160 GeneticVariation disease GWASCAT Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis. 26908601 2016
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		0.160 GeneticVariation disease BEFREE The objective of the present study was to analyze the relationship between the 6936A/G polymorphism in the EPCR gene and the occurrence of DVT. 21362311 2011
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		0.160 GeneticVariation disease BEFREE The paternal PROCR 6936G allele could be a risk factor for maternal iliac DVT. 20141580 2010
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		0.160 GeneticVariation disease BEFREE The aim of this study was to investigate whether variations in the EPCR gene or plasma sEPCR levels are risk factors for deep venous thrombosis (DVT). 15304035 2004
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		0.160 GeneticVariation disease BEFREE In conclusion, MTHFR TT677 does not appear to be an important risk factor for DVT, EPCR 403ins23 seems to be very rare, its role in the development of DVT unclear. 12413583 2002
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		0.160 GeneticVariation disease BEFREE In this study, a 23bp insertion in the EPCR gene was found in 4/198 survivors of myocardial infarction and 3/194 patients with deep vein thrombosis. 11686350 2001