Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2519093
rs2519093
ABO
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		T 0.820 GeneticVariation GWASCAT Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism. 31420334

2019
dbSNP: rs2519093
rs2519093
ABO
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		T 0.820 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: rs2519093
rs2519093
ABO
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		A 0.820 GeneticVariation GWASDB ABO re-sequencing identified 15 novel single nucleotide variations (SNV) in ABO intron 6 and the ABO 3' UTR that were strongly associated with VTE (P<10(-4)) and belonged to three distinct linkage disequilibrium (LD) blocks; none were in LD with ABO rs8176719 or rs2519093. 22672568

2012
dbSNP: rs2519093
rs2519093
ABO
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.820 GeneticVariation BEFREE ABO re-sequencing identified 15 novel single nucleotide variations (SNV) in ABO intron 6 and the ABO 3' UTR that were strongly associated with VTE (P<10(-4)) and belonged to three distinct linkage disequilibrium (LD) blocks; none were in LD with ABO rs8176719 or rs2519093. 22672568

2012
dbSNP: rs2519093
rs2519093
ABO
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		A 0.820 GeneticVariation GWASCAT ABO re-sequencing identified 15 novel single nucleotide variations (SNV) in ABO intron 6 and the ABO 3' UTR that were strongly associated with VTE (P<10(-4)) and belonged to three distinct linkage disequilibrium (LD) blocks; none were in LD with ABO rs8176719 or rs2519093. 22672568

2012
dbSNP: rs2519093
rs2519093
ABO
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.820 GeneticVariation BEFREE Among 2927 individuals, one or more SNPs within ABO, F2, F5, F11, KLKB1, SELP and SCUBE1 were significantly associated with VTE, including factor (F) V Leiden, prothrombin G20210A, ABO non-O blood type, and a novel association with ABO rs2519093 (OR=1.68, P-value=8.08×10(-16) ) that was independent of blood type. 21463476

2011