Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6025
rs6025
F5
T 0.730 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: rs6025
rs6025
F5
0.730 GeneticVariation BEFREE Furthermore, high levels of factor IX and low levels of free protein S were associated with increased risk for PE, whereas aPC resistance and F5 rs6</span>025 were risk factors for DV</span>T and not PE. 23015030

2012
dbSNP: rs6025
rs6025
F5
0.730 GeneticVariation BEFREE Low prevalence of activated protein C resistance and coagulation factor V Arg506 to Gln mutation among Korean patients with deep vein thrombosis. 9886165

1998
dbSNP: rs6025
rs6025
F5
0.730 GeneticVariation BEFREE Early saphenous vein graft occlusion after CABG could tentatively be added to deep vein thrombosis as a vascular complication that can be attributed to the factor V (Arg506-->Gln) mutation. 9716141

1998
dbSNP: rs121909567
rs121909567
SERPINC1
A 0.700 CausalMutation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019
dbSNP: rs121918156
rs121918156
PROC ; LOC105373608
T 0.700 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019
dbSNP: rs1321566264
rs1321566264
PROC ; LOC105373608
T 0.700 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019
dbSNP: rs1487411568
rs1487411568
SERPINC1 ; ZBTB37
A 0.700 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019
dbSNP: rs1553424043
rs1553424043
PROC ; MIR4783
C 0.700 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019
dbSNP: rs369504169
rs369504169
PROC
A 0.700 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019
dbSNP: rs113092656
rs113092656 		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: rs114209171
rs114209171
FUNDC2
T 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: rs17490626
rs17490626
TSPAN15
G 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: rs1799963
rs1799963
F2
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: rs34234989
rs34234989
PROCR ; MMP24-AS1-EDEM2
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: rs4444878
rs4444878
F11-AS1
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: rs529565
rs529565
ABO
C 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: rs60942712
rs60942712 		T 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: rs72798544
rs72798544
COX7A2L
G 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: rs7654093
rs7654093 		T 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: rs9797861
rs9797861
SLC44A2
T 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: rs1217691063
rs1217691063
MTHFR
0.100 GeneticVariation BEFREE Relationship between genetic polymorphism of MTHFR C677T and lower extremities deep venous thrombosis. 30303041

2019
dbSNP: rs1217691063
rs1217691063
MTHFR
0.100 GeneticVariation BEFREE Thus, the aim of the present study is to determine the prevalence of FVL, MTHFR C677T and MTHFR A1298C gene polymorphisms in patients with DVT in central Iran. 29855758

2018
dbSNP: rs1217691063
rs1217691063
MTHFR
0.100 GeneticVariation BEFREE GpIIIa 1565T/C and homozygous MTHFR 677C/T polymorphisms were higher in DVT patients compared with the control group (OR=6.65, 95% CI=3.09-14.30 and OR=4.08, 95% CI=1.35-12.38, respectively). 26261166

2015
dbSNP: rs1217691063
rs1217691063
MTHFR
0.100 GeneticVariation BEFREE PAI-1 4G/5G and MTHFR C677T polymorphisms increased the accuracy of two prediction scores for the risk of acute lower extremity deep vein thrombosis. 24715181

2014