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SNP information rs3136516

RS3136516

Normal allele: AA

Polymorphism rs3136516 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:

  21239755   Functional polymorphisms of the coagulation factor II gene (F2) and susceptibility to systemic lupus erythematosus.

  21791469   Genetic factors underlying the risk of bortezomib induced peripheral neuropathy in multiple myeloma patients.

  23029076   Association between human prothrombin variant (T165M) and kidney stone disease.

  23954867   The association of idiopathic recurrent pregnancy loss with polymorphisms in hemostasis-related genes.

  24226152   Influence of single nucleotide polymorphisms on thrombin generation in factor V Leiden heterozygotes.

  25126975   A pharmacogenetics-based warfarin maintenance dosing algorithm from Northern Chinese patients.

  28373160   Genetic Analysis of Venous Thromboembolism in UK Biobank Identifies the ZFPM2 Locus and Implicates Obesity as a Causal Risk Factor.

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

  32594420   Role of prothrombin 19911 A>G polymorphism, blood group and male gender in patients with venous thromboembolism: Results of a German cohort study.

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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