Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2289252
rs2289252
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
T 0.740 GeneticVariation GWASCAT Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism. 31420334

2019

dbSNP: rs2289252
rs2289252
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
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

dbSNP: rs2289252
rs2289252
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
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

dbSNP: rs2289252
rs2289252
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
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

dbSNP: rs2289252
rs2289252
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
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

dbSNP: rs10025152
rs10025152
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 GeneticVariation GWASDB Genetics of venous thrombosis: insights from a new genome wide association study. 21980494

2011

dbSNP: rs10029715
rs10029715
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 GeneticVariation GWASDB Genetics of venous thrombosis: insights from a new genome wide association study. 21980494

2011

dbSNP: rs1008728
rs1008728
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 GeneticVariation GWASDB Genetics of venous thrombosis: insights from a new genome wide association study. 21980494

2011

dbSNP: rs11132387
rs11132387
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 GeneticVariation GWASDB Genetics of venous thrombosis: insights from a new genome wide association study. 21980494

2011

dbSNP: rs12500826
rs12500826
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 GeneticVariation GWASDB Genetics of venous thrombosis: insights from a new genome wide association study. 21980494

2011

dbSNP: rs149130695
rs149130695
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 GeneticVariation GWASCAT Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism. 31420334

2019

dbSNP: rs4444878
rs4444878
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
A 0.700 GeneticVariation GWASCAT Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis. 26908601

2016

dbSNP: rs4572916
rs4572916
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 GeneticVariation GWASDB Genetics of venous thrombosis: insights from a new genome wide association study. 21980494

2011

dbSNP: rs907439
rs907439
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 GeneticVariation GWASDB Genetics of venous thrombosis: insights from a new genome wide association study. 21980494

2011