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SNP information rs1800595

RS1800595

Normal allele: TT

Polymorphism rs1800595 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:

  19591822   Prevalence of genetic thrombophilic polymorphisms in the Sri Lankan population--implications for association study design and clinical genetic testing services

  22540831   Candidate gene study of genetic thrombophilic polymorphisms in pre-eclampsia and recurrent pregnancy loss in Sinhalese women.

  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.

  28086795   Atherosclerotic and thrombotic genetic and environmental determinants in Egyptian coronary artery disease patients: a pilot study.

  28488549   Prevalence of F5 1691G>A, F2 20210G>A, and MTHFR 677C>T polymorphisms in Bosnian women with pregnancy loss.

  30979054   Meta-Analysis of Factor V, Factor VII, Factor XII, and Factor XIII-A Gene Polymorphisms and Ischemic Stroke.

  34087973   Bosnian Study on Markers of Ischaemic Stroke in Adults 20-50 Years Old (SMISAO): Preliminary Report.

  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.

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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