FGA, fibrinogen alpha chain, 2243

N. diseases: 118; N. variants: 20
Disease: Venous Thromboembolism ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.420 GeneticVariation phenotype BEFREE Among the genome-wide significant results, our study replicated previously known venous thromboembolism (VTE) loci near the F5, FGA-FGG, F11, F2, PROCR and ABO genes, and the more recently discovered locus near SLC44A2 In addition, our study reports for the first time a genome-wide significant association between rs114209171, located upstream of the F8 structural gene, and thrombosis risk. 26908601 2016
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.420 GeneticVariation phenotype GWASDB Genetics of venous thrombosis: insights from a new genome wide association study. 21980494 2011
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.420 Biomarker phenotype CTD_human In conclusion, our experimental data indicated that functional genetic variants in FGA are risk factors for VTE in Taiwanese populations. 16362348 2006
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.420 GeneticVariation phenotype BEFREE In conclusion, our experimental data indicated that functional genetic variants in FGA are risk factors for VTE in Taiwanese populations. 16362348 2006
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.420 GeneticVariation phenotype LHGDN In conclusion, our experimental data indicated that functional genetic variants in FGA are risk factors for VTE in Taiwanese populations. 16362348 2006