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Prothrombin gene mutation
Sample: Blood
If you get the mutation from one of your parents, you are heterozygous (you have only one abnormal copy of the Factor II gene, but the gene from your other parent is normal). In heterozygous carriers of this mutation, the risk of developing a deep vein thrombosis or pulmonary embolism is about two to three in 1,000
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People with this genetic condition have a prothrombin mutation, also called a prothrombin G20210A or a factor II mutation. Most people with prothrombin mutations will never develop an abnormal blood clot. But women who are pregnant already have a higher risk of getting a clot during and right after pregnancy.
What is the Prothrombin gene mutation in pregnancy?
People with this genetic condition have a prothrombin mutation, also called a prothrombin G20210A or a factor II mutation. Most people with prothrombin mutations will never develop an abnormal blood clot. But women who are pregnant already have a higher risk of getting a clot during and right after pregnancy.
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Choose the test you need and add it to cart .
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Book a slot for sample collection.
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