Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6025
rs6025
F5
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		T 0.900 GeneticVariation GWASCAT We developed a genome-wide polygenic risk score for venous thromboembolism that identifies 5% of the population at an equivalent incident venous thromboembolism risk to carriers of the established factor V Leiden p.R506Q and prothrombin G20210A mutations. 31676865

2019
dbSNP: rs6025
rs6025
F5
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		T 0.900 GeneticVariation GWASCAT Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism. 31420334

2019
dbSNP: rs6025
rs6025
F5
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		T 0.900 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: rs6025
rs6025
F5
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		T 0.900 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
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		T 0.900 GeneticVariation GWASCAT Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism. 25772935

2015
dbSNP: rs6025
rs6025
F5
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		T 0.900 GeneticVariation GWASCAT However, F5 was the main signal on 1q24.2 as only ABO SNPs remained significantly associated with VTE after adjusting for F5 rs6025. 22672568

2012