Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs687621
rs687621
ABO
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.800 GeneticVariation GWASDB Ischemic stroke is associated with the ABO locus: the EuroCLOT study. 23381943

2013

dbSNP: rs687621
rs687621
ABO
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
G 0.800 GeneticVariation GWASDB A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. 23650146

2013

dbSNP: rs687621
rs687621
ABO
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
G 0.800 GeneticVariation GWASCAT A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. 23650146

2013

dbSNP: rs687621
rs687621
ABO
Activated Partial Thromboplastin Time measurement
A 0.800 GeneticVariation GWASDB Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease. 22703881

2012

dbSNP: rs687621
rs687621
ABO
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.800 GeneticVariation GWASDB A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q. 22672568

2012

dbSNP: rs687621
rs687621
ABO
Activated Partial Thromboplastin Time measurement
A 0.800 GeneticVariation GWASCAT Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease. 22703881

2012

dbSNP: rs687621
rs687621
ABO
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.800 GeneticVariation GWASDB Genetics of venous thrombosis: insights from a new genome wide association study. 21980494

2011

dbSNP: rs687621
rs687621
ABO
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.800 GeneticVariation GWASCAT Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium. 20231535

2010

dbSNP: rs687621
rs687621
ABO
CUI: C2825857
Disease: Factor VIII measurement
Factor VIII measurement
0.700 GeneticVariation GWASCAT Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels. 30586737

2019

dbSNP: rs687621
rs687621
ABO
CUI: C0750880
Disease: Monocyte count result
Monocyte count result
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018

dbSNP: rs687621
rs687621
ABO
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 GeneticVariation GWASCAT Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci. 30395268

2018

dbSNP: rs687621
rs687621
ABO
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
G 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488

2018

dbSNP: rs687621
rs687621
ABO
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
0.700 GeneticVariation GWASCAT Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci. 30395268

2018

dbSNP: rs687621
rs687621
ABO
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018

dbSNP: rs687621
rs687621
ABO
Diabetes Mellitus, Non-Insulin-Dependent
G 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. 30054458

2018

dbSNP: rs687621
rs687621
ABO
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
A 0.700 GeneticVariation GWASCAT Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. 27618447

2016

dbSNP: rs687621
rs687621
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: rs687621
rs687621
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: rs687621
rs687621
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: rs687621
rs687621
ABO
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012

dbSNP: rs687621
rs687621
ABO
CUI: C0202202
Disease: Protein measurement
Protein measurement
0.700 GeneticVariation GWASDB A genome-wide association study of circulating galectin-3. 23056639

2012

dbSNP: rs687621
rs687621
ABO
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
0.700 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: rs687621
rs687621
ABO
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
Androgen-Insensitivity Syndrome
0.010 GeneticVariation BEFREE SNPs rs4513093 of CDH13 and rs687621 of ABO were found to be significantly associated with AIS with an odds ratio of 0.8691 and 1.203, respectively. 30994600

2019