$200
Blood clots can pose significant health threats. Determine if you’re at a heightened risk for abnormal clotting with the DNA Thrombotic Risk Test.
Thrombophilia is a medical condition characterized by the blood’s increased propensity to clot. Thrombosis refers to the formation of a blood clot within a vessel, which can obstruct blood flow.
Thrombophilia can manifest in various ways, depending on where a clot forms and its severity. Recognizing these symptoms early can be crucial for timely intervention and treatment. Here are the primary manifestations:
Several factors can increase an individual’s risk of developing thrombophilia. These range from health conditions and lifestyle choices to genetic predispositions. Being aware of these factors can help in prevention and early detection. Here’s a breakdown:
This test delves into the genetic variations in three genes that can influence your risk of thrombosis, a condition where blood clots form in blood vessels.
Each individual inherits two copies of every gene, one from each parent. This means that for each of the genes F5, F2, and MTHFR, you can have:
Each combination of these genes corresponds to a distinct risk level for thrombophilia.
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