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Pathology & Laboratory Medicine Prothrombin G20210A Mutation Clinical Application: Prothrombin G20210A (the prothrombin gene mutate n”) is a common gene mutation that slightly increases the circulating
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What is prothrombin g20210a mutation?
Prothrombin g20210a mutation is a genetic mutation of the prothrombin gene that increases the risk of blood clotting disorders.
Who is required to file prothrombin g20210a mutation?
There is no specific requirement to file prothrombin g20210a mutation. However, individuals who have been diagnosed with this mutation may be advised to inform their healthcare providers.
How to fill out prothrombin g20210a mutation?
Prothrombin g20210a mutation is a genetic test conducted by healthcare professionals. It involves a blood sample and laboratory analysis. Patients do not usually fill out any forms for this test.
What is the purpose of prothrombin g20210a mutation?
The purpose of testing for prothrombin g20210a mutation is to identify individuals who are at an increased risk of blood clotting disorders, such as deep vein thrombosis or pulmonary embolism.
What information must be reported on prothrombin g20210a mutation?
The prothrombin g20210a mutation test typically reports the presence or absence of the mutation in the patient's genetic material. Additional information may include the patient's risk factors or recommendations for further medical management.
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