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SNP information rs6046


Normal allele: GG

Polymorphism rs6046 is related to topics like this:

G20210A prothrombin mutation

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

Research and publications:

  10984565   Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery disease.

  12181036   Factor VII Deficiency.

  16846490   Lemierre's syndrome and genetic polymorphisms: case report

  17048007   Association of warfarin dose with genes involved in its action and metabolism

  17903294   Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.

  18403734   Polymorphisms in platelet glycoprotein 1balpha and factor VII and risk of ischemic stroke: a meta-analysis.

  18513389   New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background

  19131662   A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients

  19263529   Genetic risk factors in recurrent venous thromboembolism: A multilocus, population-based, prospective approach

  19330901   Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study

  19336475   Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk

  19404551   Association of genetic variants with myocardial infarction in Japanese individuals with chronic kidney disease.

  19415820   The effect of nine common polymorphisms in coagulation factor genes (F2, F5, F7, F12 and F13 ) on the effectiveness of statins: the GenHAT study.

  19474294   Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

  19559392   A candidate gene association study of 77 polymorphisms in migraine

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

  20417488   Association of fetal inflammation and coagulation pathway gene polymorphisms with neurodevelopmental delay at age 2 years

  20452482   Identification of fetal and maternal single nucleotide polymorphisms in candidate genes that predispose to spontaneous preterm labor with intact membranes.

  20735728   Haplotype and genotype effects of the F7 gene on circulating factor VII, coagulation activation markers and incident coronary heart disease in UK men.

  21114618   Association of coagulation-related and inflammation-related genes and factor VIIc levels with stroke: the Cardiovascular Health Study.

  21291465   The association of genetic polymorphisms with cerebral palsy: a meta-analysis.

  21676895   A gene-centric association scan for Coagulation Factor VII levels in European and African Americans: the Candidate Gene Association Resource (CARe) Consortium.

  21838885   Association between polymorphisms in the coagulation factor VII gene and coronary heart disease risk in different ethnicities: a meta-analysis.

  21881118   Genetic variants and susceptibility to neurological complications following West Nile virus infection.

  23016735   Personalized approach of medication by indirect anticoagulants tailored to the patient-Russian context: what are the prospects?

  23820649   Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease

  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.

  25813534   Association of genetic variants with hypertension in a longitudinal population-based genetic epidemiological study.

  25813695   Association of genetic variants with dyslipidemia and chronic kidney disease in a longitudinal population-based genetic epidemiological study.

  25951190   Networks in Coronary Heart Disease Genetics As a Step towards Systems Epidemiology.

  26105150   Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF.

  26791477   The effects of genes implicated in cardiovascular disease on blood pressure response to treatment among treatment-naive hypertensive African Americans in the GenHAT study.

  27589735   A Genomics-Based Model for Prediction of Severe Bioprosthetic Mitral Valve Calcification.

  28049362   Warfarin Dose Model for the Prediction of Stable Maintenance Dose in Indian Patients.

  28544373   Genetic markers for inherited thrombophilia are associated with fetal growth retardation in the population of Central Russia.

  30465841   Investigation of potential biomarkers for thrombosis related diseases in Turkish Cypriot population.

  31615384   [Hemostatic Gene Polymorphisms in Acute Coronary Syndrome with Nonobstructive Coronary Atherosclerosis].

  32684587   Association Between R353Q (rs6046) Polymorphism in Factor VII with Coronary Heart Disease.

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