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SNP information rs1613662

RS1613662

Normal allele: AA

Polymorphism rs1613662 is related to topics like this:

Factor 5 blood clotting disorder

Thrombophilia, an increased tendency to form abnormal blood clots that can obstruct blood vessels,...

G20210A prothrombin mutation

The Prothrombin G20210A mutation, also known as Factor II mutation, is a hereditary trait that...


Research and publications:

  18349091   Gene variants associated with deep vein thrombosis.

  19278955   Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach.

  19786296   Platelet glycoprotein GP VI 13254C allele is an independent risk factor of premature myocardial infarction.

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

  20227257   Polymorphisms in the platelet-specific collagen receptor GP6 are associated with risk of nonfatal myocardial infarction in Caucasians

  20526338   Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists.

  20610812   The genetics of normal platelet reactivity.

  21084706   Genetic regulation of platelet receptor expression and function: application in clinical practice and drug development.

  21232005   New gene variants associated with venous thrombosis: a replication study in White and Black Americans.

  21854539   Genetic determinants of platelet reactivity during acetylsalicylic acid therapy in diabetic patients: evaluation of 27 polymorphisms within candidate genes.

  22133274   Polymorphisms of PAI-1 and platelet GP Ia may associate with impairment of renal function and thrombocytopenia in Puumala hantavirus infection.

  22821001   Variability of GP6 gene in patients with sticky platelet syndrome and deep venous thrombosis and/or pulmonary embolism.

  22901851   Platelet aggregation abnormalities in patients with fetal losses: the GP6 gene polymorphism.

  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.

  24456740   Apolipoprotein E polymorphism is associated with lower extremity deep venous thrombosis: color-flow Doppler ultrasound evaluation.

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

  25093390   Genetic polymorphisms of platelet receptors in patients with acute myocardial infarction and resistance to antiplatelet therapy.

  25360888   Genetic determinants of on-aspirin platelet reactivity: focus on the influence of PEAR1.

  25741868   Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

  25901734   Effect of platelet receptor gene polymorphisms on outcomes in ST-elevation myocardial infarction patients after percutaneous coronary intervention.

  27143073   [Pharmacogenomics study of 620 whole-exome sequencing: focusing on aspirin application].

  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.

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

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