PROTHROMBIN (FACTOR II) MUTATION

Requirements

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    Sample Required EDTA Blood

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    Preperations Required Duly filled Genomics Clinical Information Requisition Form is mandatory.

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    Gender Male & Female

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    Age Group 0 - 99 Years

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    Collection AtHome & Lab

5200
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    1 Observations included

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    Results with in 3 Days

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PROTHROMBIN (FACTOR II) MUTATION

Observations Included

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10,000+ Tests Done

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Trusted By Doctors

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NABL Certified Labs

Overview

The prothrombin G20210A mutation is the second most common inherited predisposition to hypercoagulability. Heterozygous prothrombin G20210A mutation is associated with a 2 to 6 fold increased lifetime relative risk of VTE. This risk is further increased in combination with pregnancy and OCP use.

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