SNP information rs2289252

Research and publications:

  19552680   Common hemostasis and inflammation gene variants and venous thrombosis in older adults from the Cardiovascular Health Study.

  19583818   Genetic variants associated with deep vein thrombosis: the F11 locus.

  19682239   Replication of findings on the association of genetic variation in 24 hemostasis genes and risk of incident venous thrombosis.

  20031567   Assessing candidate inflammatory and thrombotic genes for venous thromboembolism risk: the Women's Genome Health Study.

  20174595   Personalized healthcare in clotting disorders.

  20352152   Association of common genetic variations and idiopathic venous thromboembolism. Results from EDITh, a hospital-based case-control study.

  21980494   Genetics of venous thrombosis: insights from a new genome wide association study.

  22533697   Candidate gene polymorphisms and the risk for pregnancy-related venous thrombosis.

  22633531   The F11 rs2289252 polymorphism is associated with FXI activity levels and APTT ratio in women with thrombosis.

  23124848   Brief Report: Single-nucleotide polymorphisms in VKORC1 are risk factors for systemic lupus erythematosus in Asians.

  23150947   Single nucleotide polymorphisms and the risk of venous thrombosis: results from a Danish case-cohort study.

  23650146   A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.

  25091233   Association of F11 polymorphism rs2289252 with deep vein thrombosis and related phenotypes in population of Latvia.

  25341889   Multilocus genetic risk scores for venous thromboembolism risk assessment.

  25517908   Activity of coagulation factor XI in patients with spontaneous miscarriage: the presence of risk alleles.

  26423325   F11 is associated with recurrent VTE in women. A prospective cohort study.

  27414984   Genetic risk factors for venous thrombosis in women using combined oral contraceptives: update of the PILGRIM study.

  27766050   Causes of venous thrombosis.

  28353616   Associations between polymorphisms in coagulation-related genes and venous thromboembolism: A meta-analysis with trial sequential analysis.

  29190926   Polymorphism of the ABO gene associate with thrombosis risk in patients with paroxysmal nocturnal hemoglobinuria.

  29995659   Venous thromboembolism risk associated with ABO, F11 and FGG loci.

  30168256   Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes.

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

  34207366   Cis-Segregation of c.1171C>T Stop Codon (p.R391*) in SERPINC1 Gene and c.1691G>A Transition (p.R506Q) in F5 Gene and Selected GWAS Multilocus Approach in Inherited Thrombophilia.

  34784644   The Risk of Venous Thromboembolism Attributed to Established Prothrombotic Genotypes.