Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2244
Gene Symbol: FGB
FGB
0.100 GeneticVariation disease BEFREE Our findings indicated that FGβ -148 C/T and -455 G/A polymorphisms may serve as potential biological markers for IS in Asians. 30503677 2019
Entrez Id: 2244
Gene Symbol: FGB
FGB
0.100 GeneticVariation disease BEFREE A total of nine gene variants/polymorphisms - F5 (Leiden - R5 06Q, rs6025), F2 (20210G > A, rs1799963), F13A1 (rs5985" genes_norm="2162">V34L, rs5985), MTHFR (677C > T - rs1801133;rs771406104;rs1455404812;s771406104" genes_norm="1636;2244;4524">A222V, rs1801133), MTHFR (1298A > C - rs1801131" genes_norm="4524">E429A, rs1801131), FGB (-455G > A -c.-463G > A; rs1800790), SERPINE1 (PAI14G/5G - rs1799889), ACE (ACE I/D, rs1799752), ITGB3 (GPIIIa L33P, rs5918) and the APOE E2/E3/E4 alleles (rs7412, rs429358) - were genotyped in 200 newly diagnosed ischemic stroke (IS) patients, 165 patients with ischemic coronary heart disease (CHD) and 159 controls with no cerebroor cardiovascular disease (non-CVD). 27629735 2016
Entrez Id: 2244
Gene Symbol: FGB
FGB
0.100 GeneticVariation disease BEFREE Correlation with Platelet Parameters and Genetic Markers of Thrombophilia Panel (Factor II g.20210G>A, Factor V Leiden, MTHFR (C677T, A1298C), PAI-1, β-Fibrinogen, Factor XIIIA (V34L), Glycoprotein IIIa (L33P)) in Ischemic Strokes. 26951304 2016
Entrez Id: 2244
Gene Symbol: FGB
FGB
0.100 GeneticVariation disease BEFREE Our study aimed at investigating whether the FGβ gene (-148 C/T, 448 G/A, and -854 G/A) polymorphisms were associated with susceptibility to ischemic stroke by conducting meta-analysis. 25890854 2015
Entrez Id: 2244
Gene Symbol: FGB
FGB
0.100 GeneticVariation disease BEFREE The results of our meta-analysis suggested that the -148C>T polymorphism in the FGB gene is a susceptibility marker of ischemic stroke. 25867317 2015
Entrez Id: 2244
Gene Symbol: FGB
FGB
0.100 GeneticVariation disease BEFREE The second patient, referred after ischemic stroke (functional fibrinogen 77mg/dL), had a novel heterozygous splicing mutation in intron 5 of FGB (IVS5+2T>A or c.832+2T>A), which we demonstrated to cause either exon 5 skipping or the inclusion of 75bp belonging to intron 5. 25981141 2015
Entrez Id: 2244
Gene Symbol: FGB
FGB
0.100 GeneticVariation disease BEFREE To shed light on these inconclusive findings, we performed a meta-analysis of studies relating the FGB genetic polymorphism (-148C>T) to the risk of ischemic stroke. 24720800 2014
Entrez Id: 2244
Gene Symbol: FGB
FGB
0.100 GeneticVariation disease BEFREE Results showed that the β-fibrinogen-455G/A polymorphism was significantly associated with the risk of ischemic stroke. 24366241 2014
Entrez Id: 2244
Gene Symbol: FGB
FGB
0.100 GeneticVariation disease BEFREE The results indicated that the FGB-455G/A polymorphism is associated with the risk of IS when compared with the dominant model (OR=1.518, 95%CI=1.279-1.802 for AA+GA vs. GG). 24448059 2014
Entrez Id: 2244
Gene Symbol: FGB
FGB
0.100 GeneticVariation disease BEFREE The β-fibrinogen -455G/A gene polymorphism is not a risk factor for ischaemic stroke in a Polish population. 23650004 2013
Entrez Id: 2244
Gene Symbol: FGB
FGB
0.100 GeneticVariation disease BEFREE We investigated whether common (> or = 5% minor allele frequency) variation in the fibrinogen genes (FGA, FGB, FGG) is associated with fibrinogen concentration, carotid artery intima-medial thickness (IMT) and risk of incident myocardial infarction (MI), ischemic stroke and CVD mortality in European- (EA) and African-descent (AA) adults (> or = 65 years) from the Cardiovascular Health Study. 18278190 2008
Entrez Id: 2244
Gene Symbol: FGB
FGB
0.100 GeneticVariation disease BEFREE ACE D/I, MTHFR C677T, beta-Fg -455A/G, beta-Fg -148T/C, PAI-1 4G/5G, and ApoE epsilon2-4 were associated with risk of ischemic stroke in Han Chinese. 18511872 2008
Entrez Id: 2244
Gene Symbol: FGB
FGB
0.100 AlteredExpression disease BEFREE To investigate associations between variation in the fibrinogen gamma (FGG), alpha (FGA) and beta (FGB) genes, fibrinogen level, and ischemic stroke. 18331453 2008
Entrez Id: 2244
Gene Symbol: FGB
FGB
0.100 GeneticVariation disease BEFREE Persons with the Fgbeta CT/TT, MTHFR CT/TT, and ACE ID/DD genotypes had an elevated incidence of ischemic stroke (OR 3.907, 95% CI, 1.160-13.162, P=0.028). 16443328 2006
Entrez Id: 2244
Gene Symbol: FGB
FGB
0.100 GeneticVariation disease BEFREE Contribution of the -455G/A polymorphism at beta-fibrinogen gene and of the Leiden mutation to hemorheological parameters in ischemic stroke patients. 16899909 2006
Entrez Id: 2244
Gene Symbol: FGB
FGB
0.100 GeneticVariation disease BEFREE Plasma fibrinogen expression is affected by the beta-fibrinogen gene -455A/G polymorphism, and the H2 allele may be a risk factor for ischemic stroke in Chinese males. 11940334 2002
Entrez Id: 2244
Gene Symbol: FGB
FGB
0.100 GeneticVariation disease BEFREE We investigated the associations between ischemic stroke, plasma fibrinogen level, and a HaeIII restriction fragment length polymorphism (G/A(-455)) located at -455 bp from the start of transcription of the beta fibrinogen gene in 85 hypertensive patients with ischemic stroke (stroke group), 85 hypertensive patients without ischemic stroke (nonstroke group) and in 84 normotensive subjects matched for age, sex, and smoking status recruited at an annual health examination (normotensive group). 9690809 1998
Entrez Id: 2244
Gene Symbol: FGB
FGB
0.100 GeneticVariation disease BEFREE The apolipoprotein E and beta-fibrinogen G/A-455 gene polymorphisms are associated with ischemic stroke involving large-vessel disease. 9409270 1997