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SNP information rs2066865

RS2066865

Normal allele: GG

Genetic variability in the fibrinogen-gamma FGG gene increases the risk of deep vein thrombosis by reducing plasma fibrinogen-gamma levels.

Polymorphism rs2066865 is related to topics like this:

G20210A prothrombin mutation

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Research and publications:

  16144795   Genetic variation in the fibrinogen gamma gene increases the risk of deep vein thrombosis by reducing plasma gamma fibrinogen levels.

  17445871   The fibrinogen gamma (FGG) 10034C>T polymorphism is associated with venous thrombosis.

  20059469   Interaction between fibrinogen and IL-6 genetic variants and associations with cardiovascular disease risk in the Cardiovascular Health Study.

  20167083   Fibrinogen beta variants confer protection against coronary artery disease in a Greek case-control study.

  20709368   The fibrinogen gamma 10034C>T polymorphism is not associated with Peripheral Arterial Disease.

  20978265   Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe).

  21422408   Clotting factor gene polymorphisms and colorectal cancer risk.

  21757653   Assessing genetic determinants of the association of β-fibrinogen with cardiovascular disease.

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

  22707612   Genetic risk factors for thrombosis in systemic lupus erythematosus.

  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.

  25613928   Contribution of genetic and environmental factors to changes in total and β-fibrinogen over 5 years.

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

  26916295   A prospective study of β-fibrinogen and the incidence of venous thromboembolism: the Longitudinal Study of Thromboembolism Etiology (LITE).

  27766050   Causes of venous thrombosis.

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

  29094466   Joint effects of prothrombotic genotypes and body height on the risk of venous thromboembolism: the Tromsø study.

  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.

  30773804   Effect of prothrombotic genotypes on the risk of venous thromboembolism in patients with and without ischemic stroke. The Tromsø Study.

  31124268   Impact of prothrombotic genotypes on the association between family history of myocardial infarction and venous thromboembolism.

  31484330   Polymorphism rs2066865 in the Fibrinogen Gamma Chain (FGG) Gene Increases Plasma Fibrinogen Concentration and Is Associated with an Increased Microvascular Thrombosis Rate.

  31582554   Fibrinogen gamma gene rs2066865 and risk of cancer-related venous thromboembolism.

  31689458   Venous thromboembolism GWAS reported genetic makeup and the hallmarks of cancer: Linkage to ovarian tumour behaviour.

  32110755   Myocardial infarction, prothrombotic genotypes, and venous thrombosis risk: The Tromsø Study.

  32342502   The joint effect of genetic risk factors and different types of combined oral contraceptives on venous thrombosis risk.

  32402998   Prothrombotic genotypes and risk of major bleeding in patients with incident venous thromboembolism.

  32671915   Combined effects of five prothrombotic genotypes and cancer on the risk of a first venous thromboembolic event.

  33776563   Association of fibrinogen and plasmin inhibitor, but not coagulation factor XIII gene polymorphisms with coronary artery disease.

  33940655   Joint Effect of Multiple Prothrombotic Genotypes and Obesity on the Risk of Incident Venous Thromboembolism.

  34200207   Genetic Risk Profiling Associated with Recurrent Unprovoked Venous Thromboembolism.

  34263111   Predictive Ability of a Clinical-Genetic Risk Score for Venous Thromboembolism in Northern and Southern European Populations.

  34765649   The Higher Prevalence of Venous Thromboembolism in the Hungarian Roma Population Could Be Due to Elevated Genetic Risk and Stronger Gene-Environmental Interactions.

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

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