Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs514659
rs514659
ABO
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		C 0.800 GeneticVariation GWASDB Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. 21239051

2011
dbSNP: rs514659
rs514659
ABO
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		C 0.800 GeneticVariation GWASCAT Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. 21239051

2011
dbSNP: rs514659
rs514659
ABO
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178

2013
dbSNP: rs514659
rs514659
ABO
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test) 		0.700 GeneticVariation GWASDB Ischemic stroke is associated with the ABO locus: the EuroCLOT study. 23381943

2013
dbSNP: rs514659
rs514659
ABO
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 GeneticVariation GWASDB Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis. 22675575

2012
dbSNP: rs514659
rs514659
ABO
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012
dbSNP: rs514659
rs514659
ABO
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 GeneticVariation GWASDB A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q. 22672568

2012
dbSNP: rs514659
rs514659
ABO
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 GeneticVariation GWASDB A genome-wide association study of circulating galectin-3. 23056639

2012
dbSNP: rs514659
rs514659
ABO
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 GeneticVariation GWASDB A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation. 22291609

2012
dbSNP: rs514659
rs514659
ABO
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: rs514659
rs514659
ABO
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		C 0.700 GeneticVariation GWASCAT Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. 21239051

2011
dbSNP: rs514659
rs514659
ABO
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.010 GeneticVariation BEFREE We selected four single nucleotide polymorphisms (rs579459, rs651007, rs514659 and rs529565) of the ABO gene and performed genotyping assays to assess the association with ischemic stroke and its subtypes. 27542834

2016