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SNP information rs710446

RS710446

Normal allele: TT

Polymorphism rs710446 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:

  20303064   Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time.

  20876611   Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ.

  21270443   KNG1 Ile581Thr and susceptibility to venous thrombosis.

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

  22701019   A genome-wide association study identifies KNG1 as a genetic determinant of plasma factor XI Level and activated partial thromboplastin time.

  25341889   Multilocus genetic risk scores for venous thromboembolism risk assessment.

  25779970   Gene-centric approach identifies new and known loci for FVIII activity and VWF antigen levels in European Americans and African Americans.

  26159646   Variants in the Atherogenic ALOX5AP, THBD, and KNG1 Genes Potentiate the Risk of Ischemic Stroke via a Genetic Main Effect and Epistatic Interactions in a Chinese Population.

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

  28053049   Genome-wide association study with additional genetic and post-transcriptional analyses reveals novel regulators of plasma factor XI levels.

  28445521   Next generation sequencing to dissect the genetic architecture of KNG1 and F11 loci using factor XI levels as an intermediate phenotype of thrombosis.

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

  30478260   Genetic effects of BDKRB2 and KNG1 on deep venous thrombosis after orthopedic surgery and the potential mediator.

  32270254   Decreased plasma kallikrein activity is associated with reduced kidney function in individuals with type 1 diabetes.

  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.

  34979665   Cryptogenic Stroke in the Young: Role of Candidate Gene Polymorphisms in Indian Patients with Ischemic Etiology.

Schizophrenia is it genetic

A psychosis known as schizophrenia impacts an individual's thinking, sense of self, and...

Hereditary polyneuropathy

The peripheral nervous system is affected by a diverse range of diseases known as hereditary...

Melanoma genes

The incidence of malignant melanoma (MM) is rising sharply, making it one of the most aggressive...

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