|
rs2036914
|
|
|
0.830 |
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 |
|
rs2036914
|
|
|
0.830 |
GeneticVariation |
BEFREE |
The meta-analysis revealed that the F11 rs2289252, F11 rs2036914, FGG rs2066865, and CYP4V2 rs13146272 polymorphisms were closely related to the development of VTE in the white race under the best genetic models after multiple testing adjustments.
|
28353616 |
2017 |
|
rs2036914
|
|
|
0.830 |
GeneticVariation |
BEFREE |
In F11, the CC genotype for rs2036914 and the CT and TT genotypes for rs2289252 were associated with a significantly higher VTE risk.
|
23150947 |
2013 |
|
rs3756008
|
|
|
0.810 |
GeneticVariation |
BEFREE |
A nucleotide variant (rs3756008) in the promoter region of the FXI gene was recently reported for association with venous thromboembolism.
|
24420855 |
2014 |
|
rs2289252
|
|
|
0.740 |
GeneticVariation |
BEFREE |
The meta-analysis revealed that the F11 rs2289252, F11 rs2036914, FGG rs2066865, and CYP4V2 rs13146272 polymorphisms were closely related to the development of VTE in the white race under the best genetic models after multiple testing adjustments.
|
28353616 |
2017 |
|
rs2289252
|
|
|
0.740 |
GeneticVariation |
BEFREE |
In conclusion, F5 rs6025 and F11 rs2289252 contributed to the risk of recurrent VTE and the combination is of potential clinical relevance for risk prediction.
|
26423325 |
2016 |
|
rs2289252
|
|
|
0.740 |
GeneticVariation |
BEFREE |
Seven SNPs (F5 rs6025, F2 rs1799963, ABO rs514659, FGG rs2066865, F11 rs2289252, PROC rs1799810 and KNG1 rs710446) with four SNP-SNP interactions contributed to the genetic risk score for VTE, with an AUC of 0.66 (95% CI, 0.64-0.68).
|
25472531 |
2015 |
|
rs2289252
|
|
|
0.740 |
GeneticVariation |
BEFREE |
In F11, the CC genotype for rs2036914 and the CT and TT genotypes for rs2289252 were associated with a significantly higher VTE risk.
|
23150947 |
2013 |
|
rs925451
|
|
|
0.710 |
GeneticVariation |
BEFREE |
After Bonferroni adjustment, four single nucleotide polymorphisms (SNPs) were significantly associated with VTE: Factor XI rs925451 polymorphism, factor XI rs2289252 polymorphism, factor II rs1799963 (G20210A) polymorphism and factor V Leiden rs6025.
|
20352152 |
2010 |