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Venous thromboembolism (VTE) is a syndrome of deep vein thrombosis and its complication, pulmonary embolism. The prothrombin (PT) G20210A mutation (F2 rs1799963) is a common polymorphism within the 3’ untranslated region of the prothrombin gene, affecting 1.5% to 3% of Caucasian Americans, especially persons of southern European ancestry. The PT G20210A allele is uncommon among African Americans (carrier frequency of 0.4%). The PT G20210A mutation is associated with a 3-fold increased risk of venous thromboembolism due to increased plasma prothrombin activity among carriers.
The PT G20210A gene mutation test is a direct mutation analysis of patient blood leukocyte genomic DNA. At present, there are no other methods of detecting this VTE risk factor except for direct mutation testing.
Direct mutation analysis for the prothrombin (PT) G20210A allele should be reserved for patients with clinically suspected thrombophilia. There may be additional indications for direct PT G20210A mutation testing, such as in determining the duration of anticoagulation therapy of venous thromboembolism patients and screening for women contemplating hormone therapy.
The interpretive report will include sample information, assay information, background information, and conclusions drawn from the test results (normal, heterozygous prothrombin [PT] G20210A, homozygous PT G20210A).
This direct mutation analysis will not detect individuals with thrombophilia caused by mechanisms other than the prothrombin (PT) G20210A mutation. Special Coagulation Clinic, Thrombophilia Center, and/or Medical Genetics consultations are available for Mayo Clinic patients and may be especially helpful in complex cases or in situations in which the diagnosis is atypical or uncertain. Genetic counseling is recommended before testing asymptomatic family members.
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