Disease: Venous Thromboembolism ×
Source: INFERRED ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.200 GeneticVariation phenotype GWASCAT Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease. 31676865 2019
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.200 GeneticVariation phenotype GWASCAT Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism. 31420334 2019
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.200 GeneticVariation phenotype GWASCAT Genetic Analysis of Venous Thromboembolism in UK Biobank Identifies the ZFPM2 Locus and Implicates Obesity as a Causal Risk Factor. 28373160 2017
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.200 GeneticVariation phenotype 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: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.200 GeneticVariation phenotype GWASCAT Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism. 25772935 2015
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.200 GeneticVariation phenotype GWASCAT A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. 23650146 2013
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.200 GeneticVariation phenotype GWASDB A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. 23650146 2013
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.200 GeneticVariation phenotype GWASCAT A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q. 22672568 2012
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.200 GeneticVariation phenotype GWASDB A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q. 22672568 2012
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.200 GeneticVariation phenotype GWASCAT Genetics of venous thrombosis: insights from a new genome wide association study. 21980494 2011
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.200 GeneticVariation phenotype GWASDB Genetics of venous thrombosis: insights from a new genome wide association study. 21980494 2011
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.200 GeneticVariation phenotype GWASCAT Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach. 19278955 2009
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.200 GeneticVariation phenotype GWASDB Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach. 19278955 2009