Variant: rs687289 

    present in Gene: ABO
    present in Chromosome: 9
    Position on Chromosome: 133261703
    Alleles of this Variant: A/G

rs687289 in ABO gene and Activated Partial Thromboplastin Time measurement PMID 29403010 2018 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.

rs687289 in ABO gene and C-reactive protein measurement PMID 22291609 2012 A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation.

rs687289 in ABO gene and Coagulation factor measurement PMID 23267103 2013 Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.

rs687289 in ABO gene and Factor VII measurement PMID 23267103 2013 Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.

rs687289 in ABO gene and Factor VIII measurement PMID 30586737 2019 Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels.

PMID 20231535 2010 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.

rs687289 in ABO gene and Monocyte count procedure PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs687289 in ABO gene and Monocyte count result PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs687289 in ABO gene and Pancreatic carcinoma PMID 25086665 2014 Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer.

rs687289 in ABO gene and Polysomnography PMID 23251661 2012 Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.

rs687289 in ABO gene and Protein measurement PMID 23056639 2012 A genome-wide association study of circulating galectin-3.

rs687289 in ABO gene and Pseudocholinesterase Measurement PMID 21239051 2011 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.

rs687289 in ABO gene and Serum albumin measurement PMID 23281178 2013 A genome-wide assessment of variability in human serum metabolism.

rs687289 in ABO gene and Venous Thromboembolism PMID 21980494 2011 Genetics of venous thrombosis: insights from a new genome wide association study.

PMID 22672568 2012 A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.

PMID 31420334 2019 Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism.

rs687289 in ABO gene and Venous Thrombosis PMID 22675575 2012 Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis.

rs687289 in ABO gene and von Willebrand's factor (lab test) PMID 30586737 2019 Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels.

PMID 23381943 2013 Ischemic stroke is associated with the ABO locus: the EuroCLOT study.