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Genetic

Factor II / Prothrombin Mutation (G20210A) LIS Code: F II (G20210A)

Screen for the Factor II prothrombin mutation with private genetic testing for clotting risk evaluation.

→ 15 days → UKAS-accredited lab → No GP referral needed
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Test Price
£94
Results in
15 days
from sample receipt at lab
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Sample
Blood
£94
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⏱ Results in 15 days · LIS: F II (G20210A)
ℹ️ TAT begins when your sample is received at our lab.
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Phlebotomy Fee: £25
A one-off £25 phlebotomy fee applies per visit — this covers your blood draw regardless of how many tests you book in the same appointment.

Test Categories

Genetic Genetics Clotting Disorders Thrombosis Cardiovascular System Hematology

About this test

G20210A Genetic Testing for Blood Clot Risk in Slough

What is the G20210A Mutation?
The G20210A mutation is a specific genetic change in the Factor II gene, which provides instructions for producing prothrombin — a protein essential for blood clotting. This mutation can lead to elevated levels of prothrombin in the blood, increasing the risk of abnormal clot formation.

Purpose of the G20210A Genetic Test
The G20210A genetic test is a laboratory test used to detect the presence of this mutation. It helps identify individuals who may be at a higher risk of developing blood clots, particularly conditions such as:

Deep Vein Thrombosis (DVT)

Pulmonary Embolism (PE)

Other thrombotic complications

Who Should Consider G20210A Testing in Slough?
This test is recommended for individuals in Slough and nearby areas such as Windsor, Langley, and Maidenhead who have:

A personal or family history of blood clots

Experienced a blood clot at a young age

Had unexplained or recurrent episodes of thrombosis

Been diagnosed with other clotting disorders

Pregnancy complications or are undergoing fertility treatments

Conditions Related to the G20210A Mutation
In addition to increasing the risk of thrombosis, the G20210A mutation may also contribute to or be associated with:

Factor II (prothrombin) thrombophilia

Factor II deficiency

Antithrombin III deficiency (when combined with other genetic risks)

How the Test is Performed
The G20210A test is a genetic screening conducted using a blood sample or cheek swab. The sample is analysed to determine whether one or both copies of the gene carry the mutation.

Private Thrombophilia Testing in Slough
Local clinics in Slough offer confidential and accurate G20210A testing, with no GP referral required. Testing is available as part of a full thrombophilia screen or a targeted genetic panel for clotting disorders.

Book Your G20210A Genetic Test in Slough Today
If you're concerned about blood clot risks or have a family history of thrombosis, book a G20210A genetic test in Slough. Early detection can guide preventative care, lifestyle changes, or medication to reduce the likelihood of serious clotting events.

Our Professional Services Our diagnostic testing is carried out by Medical Diagnosis, a UKAS ISO 15189 accredited laboratory, ensuring all results meet the highest UK standards of quality and accuracy. Clinical consultations and treatments, including Testosterone Replacement Therapy (TRT) and Weight Management programmes, are delivered through Medical Diagnosis Victoria, which is registered with the Care Quality Commission (CQC). All clinical services are provided by GMC-registered doctors with extensive experience, following thorough medical assessment in line with UK regulatory standards.
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