Gene: FGG ×
Source: BEFREE ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2066865
rs2066865
FGG
0.860 GeneticVariation BEFREE Fibrinogen gamma gene rs2066865 and risk of cancer-related venous thromboembolism. 31582554

2019
dbSNP: rs2066865
rs2066865
FGG
0.860 GeneticVariation BEFREE Our findings suggest that the risk of VTE by FHMI is not explained by rs8176719 (ABO), rs6025 (F5), rs1799963 (F2), rs2066865 (FGG), and rs2036914 (F11). 31124268

2019
dbSNP: rs2066865
rs2066865
FGG
0.860 GeneticVariation BEFREE A nominal significant association with VTE was found for the FGG rs2066865 minor T-allele in the dominant model (OR 1.82; P = 0.034). 29995659

2018
dbSNP: rs2066865
rs2066865
FGG
0.860 GeneticVariation BEFREE Finally, our study demonstrated the important role of rs2289252, rs2036914, rs2066865, and rs13146272 polymorphisms in the development of VTE in the white race. 28353616

2017
dbSNP: rs2066865
rs2066865
FGG
0.860 GeneticVariation BEFREE In both race groups, the minor allele of FGG rs2066865 was associated with lower γ' fibrinogen concentrations, but this allele was not associated with VTE. 26916295

2016
dbSNP: rs2066865
rs2066865
FGG
0.860 GeneticVariation BEFREE We investigated the VTE risk associated with SNPs in the GP6 (rs1613662), SERPINC1 (rs2227589), F11 (rs2036914 and rs2289252), FGG (rs2066865), and F12 (rs1801020) genes. 23150947

2013