GPIIIa (HPA1a/b, L33P)
Understand your risk of platelet disorders, one gene at a time
Service Description
PCR-Hybridization: Glycoprotein Polymorphism (GPIIIa ) is a protein found on the surface of platelets that is involved in platelet aggregation and clot formation. The HPA1a/b polymorphism, also known as L33P, is a common genetic variation in the GPIIIa gene that results in the substitution of proline (Pro) for leucine (Leu) at position 33 of the protein. The HPA1a/b polymorphism has been associated with increased platelet activation and aggregation, which may contribute to an increased risk of thrombotic events such as myocardial infarction, stroke, and venous thromboembolism. However, the evidence for this association is not consistent across all studies, and other factors such as age, sex, and other genetic and environmental factors may also play a role. Testing for the HPA1a/b polymorphism may be useful in identifying individuals who may be at increased risk of thrombotic events, particularly in the context of other risk factors such as smoking, obesity, or a family history of cardiovascular disease. Sample: BLOOD Results:2 weeks Phlebotomy fee: £15 (included in price)
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Contact Details
305 Neasden Lane, London NW10 1QR, UK
02071268511
info@ejbio.co.uk
E & J Bio UK Ltd
305 Neasden Lane, London, NW10 1QR
t 0207 126 8511 | e info@ejbio.co.uk
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