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This genetic test identifies the Factor V Leiden mutation associated with increased blood clot risk. It helps assess inherited thrombophilia.
Turnaround time
2 weeks
Biomarkers count
1
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SelectedFactor V Leiden Mutation Test | London Blood Tests
Detect inherited clotting risk with our Factor V Leiden genetic blood test for £198. UKAS-accredited testing and optional GP consultation.
The Factor V Leiden Mutation Test is a genetic blood test used to identify an inherited risk of abnormal blood clotting (thrombophilia). It detects the Factor V Leiden mutation, a common cause of deep vein thrombosis (DVT) and pulmonary embolism (PE). Testing is performed in a UKAS-accredited laboratory, with an optional GP consultationfor interpretation.
Factor V is a clotting protein that plays a critical role in the blood coagulation cascade. The Factor V Leiden mutationcauses resistance to activated protein C (APC) — a natural anticoagulant — leading to a higher tendency for blood clot formation.
This mutation is inherited and lifelong. Individuals may carry:
One copy (heterozygous) – moderately increased clot risk
Two copies (homozygous) – significantly increased clot risk (less common)
Factor V Leiden is the most common inherited thrombophilia in people of European ancestry and is frequently tested in individuals with unexplained clots or strong family history of thrombosis.
At London Blood Tests, this mutation is detected using validated molecular genetic techniques aligned with UK haematology standards.
Identifies Inherited Thrombophilia
Confirms whether you carry a genetic mutation associated with increased clot risk.
Explains Unprovoked Blood Clots
Helps identify the cause of DVT or PE without obvious triggers.
Supports Pregnancy Risk Assessment
Relevant for recurrent miscarriage, placental complications, and pregnancy-related thrombosis.
Guides Preventive Care Decisions
Results may influence anticoagulation use during surgery, pregnancy, or prolonged travel.
Informs Family Screening
First-degree relatives may consider testing if the mutation is detected.
One-Time Lifetime Test
As a genetic test, it only needs to be performed once.
Optional GP Consultation for Interpretation
Results can be reviewed with a GP to explain risks and preventive strategies.
You may benefit from this test if you:
Have had an unexplained deep vein thrombosis or pulmonary embolism
Developed blood clots at a young age
Have a strong family history of blood clots
Experienced recurrent miscarriage or pregnancy complications
Are considering hormonal contraception or HRT
Are planning major surgery or prolonged immobilisation
Common symptoms of blood clots include:
Swelling, pain, or redness in one leg
Warmth over the affected area
Sudden shortness of breath
Chest pain
Rapid heartbeat
Early identification allows personalised risk management and informed medical decisions.
Book Your Appointment
Book online or by phone at your chosen clinic.
No fasting required.
Pre-Test Review
Inform the clinician of any personal or family history of clotting.
Sample Collection
A trained phlebotomist collects a venous blood sample.
Takes approximately 5–10 minutes.
Laboratory Genetic Analysis
Sample analysed in a UKAS-accredited laboratory using molecular techniques.
Quality Control
Results undergo strict verification and validation.
Results Delivery
Results typically available within 10–14 business days.
Optional GP Consultation
Review implications, prevention strategies, and next steps with a GP.
Book Your Visit
Arrange a phlebotomist home or hotel visit at a convenient time.
Professional Collection
Certified phlebotomist collects your blood sample safely.
Secure Transport
Sample couriered the same day to the laboratory.
Laboratory Testing
Genetic analysis identical to clinic testing.
Results & Follow-Up
Results delivered online, with optional GP review.
Results are reported as mutation detected or not detected.
Possible outcomes:
No mutation detected: normal Factor V gene
Heterozygous mutation: one copy detected – increased clot risk
Homozygous mutation: two copies detected – high clot risk
Interpretation notes:
Carrying the mutation does not guarantee a clot will occur
Risk increases with additional factors such as smoking, pregnancy, surgery, or oestrogen therapy
Results should be considered alongside other thrombophilia markers if indicated.
Simple steps to get your results
Choose your test online and book in seconds. Select your preferred clinic location or home visit option.
Attend one of our UK or London clinics, arrange a home nurse visit, or use a finger-prick kit where available.
Your sample is analysed by accredited UK laboratories, with secure results delivered directly to you.
Take control of your health with London Blood Tests
WhatsApp UsFollow these guidelines for accurate results
Where possible, attend your blood test between 7am and 12pm. Please wait until any short-term illness or infection has fully resolved before testing. Avoid intense exercise for 24–48 hours beforehand, as this can affect certain markers.
Fasting is not always required, but some tests may recommend it. If fasting is advised, avoid food for 8–12 hours before your appointment and drink water only. Stay well hydrated, as this helps with sample collection and accuracy.
Continue prescribed medications unless advised otherwise by your clinician. Avoid vitamin, mineral, or biotin supplements for at least 24–48 hours before your test, as these can interfere with results. If you are unsure about any medication or supplement, please let us know before your appointment.
For hormone-related tests, timing within your menstrual cycle may be important. If relevant, follow any specific guidance provided on your test page.
If you have any questions or special circumstances, our team is happy to advise before your appointment.
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