Test Price
800 AED✅ Home Collection Available
Factor V Leiden (F5 G1691A) Mutation Screening in UAE | 800 AED | DHA Licensed
Executive Summary & Core Metrics
This molecular diagnostic assay detects the G1691A variant in the F5 gene, establishing the most prevalent inherited thrombophilia risk factor. The test delivers 99.9% diagnostic sensitivity through ISO‑accredited laboratory processing and includes confirmatory whole genome sequencing.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection & VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
- Insurance Direct Billing: Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
Factor V Leiden mutation screening identifies the F5 G1691A single‑nucleotide substitution, the most common inherited thrombophilia among individuals of European descent. The assay employs real‑time PCR targeting the Factor V gene, followed by orthogonal confirmation via whole genome sequencing to eliminate false‑positive calls. Results are reported as homozygous normal, heterozygous, or homozygous mutant, with an interpretative summary for clinical risk stratification.
The test is performed on a peripheral whole blood specimen collected under strict cold‑chain conditions. Turnaround time is 3–4 working days from sample receipt. The methodology adheres to CLSI MM03‑A2 guidelines for molecular diagnostic validation.
| Feature | DNA Labs UAE | Closest Alternative |
|---|---|---|
| Precision | Real-Time PCR + WGS confirmation | Standard PCR only |
| Methodology | ISO 9001:2015 certified reagents & sequencing | Generic kits, no ISO certification |
| Turnaround Time | 3–4 working days | 5–7 working days |
| Price | 800 AED (all‑inclusive) | Often >1,000 AED |
| Home Collection | VIP mobile phlebotomy, cold chain | Limited or no home service |
Physician Insight & Safety Protocols
“As a Consultant in Medical Genetics, I recognize that receiving a positive Factor V Leiden result can provoke understandable concern. This genetic variant denotes an elevated, but not deterministic, risk for venous thromboembolism and must be interpreted alongside the patient’s personal and family thrombotic history, concomitant medications, and lifestyle factors. I strongly encourage you to review these findings with your primary care physician before initiating or altering any prophylactic regimen.” — Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Advisory – Medication Safety
Do not discontinue or alter any prescribed medication without consulting your doctor. Abrupt cessation of anticoagulant therapy can precipitate life‑threatening thromboembolic events. Always consult your prescribing physician before making any changes.
Exclusion Criteria & Emergency Red Flags
- Exclusion: Individuals with confirmed acute thrombosis, recent major surgery (within 30 days), or inability to provide informed consent under UAE PDPL are not eligible for home collection.
- Emergency Red Flags: Sudden unilateral leg swelling or pain, acute chest pain, unexplained shortness of breath, or hemoptysis warrant immediate emergency department evaluation.
Patient FAQ & Clinical Guidance
1. What is Factor V Leiden mutation screening and why is it important?
Factor V Leiden screening detects the F5 G1691A mutation, which raises your risk for dangerous blood clots. Performed on a peripheral blood sample, it guides personalized prevention, pregnancy planning, and peri‑operative care decisions.
2. Do I need a doctor’s prescription for this test?
A physician’s prescription is required for Factor V Leiden testing. Exceptions may apply for pre‑operative evaluation, pregnancy management, or travel‑related thrombosis risk assessment. Our team verifies eligibility at the time of booking in compliance with UAE regulations.
3. How long will it take to receive my results?
You will receive Factor V Leiden results within 3 to 4 working days after collection. Reports are encrypted and shared via secure portal, with optional telephonic interpretation by a licensed clinician.
4. Will my insurance cover the cost of this test?
Coverage varies by insurer and policy. Our billing team can verify your direct billing eligibility via WhatsApp at +971 54 548 8731 before sample collection.
5. How should I prepare for the blood draw?
No special preparation such as fasting is required for Factor V Leiden genetic testing. Maintain your usual hydration and medication schedule unless otherwise directed by your physician.
UAE Regulatory & Data Privacy Adherence
- Data Privacy: All genetic data is processed in full compliance with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields.
- Medical Liability: Clinical safety and patient consent protocols adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability.
- Quality Certification: Laboratory processing is conducted in an ISO 9001:2015 certified facility (Cert: INT/EGQ/2509DA/3139).
- Collection Protocol: VIP mobile phlebotomy is available daily from 8 AM to 11 PM under temperature‑controlled cold‑chain logistics. WhatsApp support: +971 54 548 8731.
Clinical & Logistical Metadata
| Test Name | Factor V Leiden (F5 G1691A) Mutation Screening |
| Price (AED) | 800 |
| Turnaround Time | 3–4 working days |
| Sample Type / Matrix | Peripheral Whole Blood (VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection Available) |
| Methodology Used | Real-Time PCR with Confirmatory Whole Genome Sequencing |
| ICD-10-CM Code | D68.51, Z14.01, D68.5 |
| LOINC Code | 57751-6 |
| DHA Facility License & Laboratory Address | DHA License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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