Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799963
rs1799963
F2
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.730 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: rs1799963
rs1799963
F2
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		A 0.730 GeneticVariation GWASCAT Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease. 31676865

2019
dbSNP: rs1799963
rs1799963
F2
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.730 GeneticVariation GWASCAT Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism. 31420334

2019
dbSNP: rs1799963
rs1799963
F2
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		A 0.730 GeneticVariation GWASCAT Genetic Analysis of Venous Thromboembolism in UK Biobank Identifies the ZFPM2 Locus and Implicates Obesity as a Causal Risk Factor. 28373160

2017
dbSNP: rs1799963
rs1799963
F2
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		A 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: rs1799963
rs1799963
F2
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		A 0.730 GeneticVariation GWASCAT Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism. 25772935

2015
dbSNP: rs1799963
rs1799963
F2
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.730 GeneticVariation BEFREE Factor V Leiden (FVL or rs6025) and prothrombin gene G20210A (PT or rs1799963) are the genetic variants currently tested for VTE risk assessment. 25341889

2014
dbSNP: rs1799963
rs1799963
F2
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.730 GeneticVariation BEFREE Apart from F5 rs6025, ABO rs8176719, rs2519093 and F2 rs1799963, additional common and high VTE-risk SNPs among whites are unlikely. 22672568

2012