Test Price
6,000 AED✅ Home Collection Available
Whole Exome + Mitochondrial Genome Sequencing in UAE | 7000 AED | DHA Accredited Lab
Executive Summary & Core Metrics
Diagnostic sensitivity exceeding 99.9% via ISO accredited processing, combined with premium temperature-controlled home collection logistics and post-test clinical guidance.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
This advanced next-generation sequencing test simultaneously analyzes the entire coding region (exome) plus the complete mitochondrial genome. The combined analysis delivers unparalleled insight into hereditary disorders, cancer predisposition, and mitochondrial syndromes that are frequently missed by standard exome-only testing. Detection of cryptic variants in the mitochondrial genome increases diagnostic yield by 15–20% for patients with complex or undiagnosed conditions.
| Feature | Our Test (Whole Exome + mtDNA) | Standard Whole Exome Sequencing |
|---|---|---|
| Precision | Dual-genome analysis (nuclear + mitochondrial) | Nuclear exome only; mitochondrial genome missed entirely |
| Methodology | NGS with proprietary enrichment and deep sequencing | NGS limited to exonic regions |
| Turnaround Time | 3–4 weeks with comprehensive report | 4–6 weeks, often without mtDNA interpretation |
Physician Insight & Safety Protocols
Lina Osama Zaki Quteineh | Consultant Medical Genetics | DHA Registration ID: 9294403
Genomic results must be interpreted within the full clinical context, integrating family history and physical findings. This test reveals predisposition, not destiny, and can guide preventive strategies. Please discuss findings with your specialist before making any medical or lifestyle changes. The dual-genome approach is particularly valuable for patients with suspected mitochondrial disease, unexplained neurological symptoms, or cancer susceptibility syndromes.
Exclusion Criteria & Emergency Red Flags
- Recent blood transfusion or bone marrow transplant within the last 6 months may affect results; please inform our team.
- This test is not intended for acute emergency diagnosis. Seek immediate emergency care if you experience severe chest pain, breathing difficulties, sudden neurological changes, or uncontrolled bleeding.
- Pregnancy or recent severe illness does not exclude testing but should be noted in clinical details to aid interpretation.
Medication Advisory
Do not discontinue prescribed medication without consulting your doctor. Genetic insights may inform but never replace clinical judgment. Always discuss any treatment modifications with your primary care physician.
Patient FAQ & Clinical Guidance
1. What is the purpose of Whole Exome + Mitochondrial Genome Sequencing?
Analyzing all exons plus mitochondrial DNA identifies rare genetic disorders, cancer susceptibility variants, and mitochondrial syndromes with high accuracy. The combined analysis increases diagnostic yield by 15–20% over exome-only tests, particularly for mitochondrial diseases and cryptic hereditary cancer syndromes, providing a comprehensive genomic picture.
2. How should I prepare for the blood collection?
No fasting is required; however, inform your doctor about recent transfusions or bone marrow transplants beforehand. Our VIP phlebotomist will collect a small blood sample in a comfortable home visit between 8 AM and 11 PM, ensuring temperature-controlled cold-chain transport to the lab. The entire process is designed for minimal discomfort and maximum sample integrity.
3. When will I receive the results and how are they interpreted?
Results typically arrive in 3–4 weeks with a comprehensive clinical report and genetic counseling advice. Our board-certified geneticist provides a telephonic consultation to explain findings, answer questions, and recommend next steps with your primary physician. The report includes variant classifications, inheritance patterns, and actionable clinical recommendations.
4. Is genetic counseling included with the test?
Yes, post-test genetic counseling is included in the service. Our consultant medical geneticist will guide you through the implications of your results, potential cascade testing for family members, and preventive health strategies. This ensures you fully understand your genomic profile and can make informed decisions.
UAE Regulatory & Data Privacy Adherence
Regulatory Compliance: This laboratory service fully complies 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. Clinical testing safety and patient consent processes adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. All genetic data is encrypted and stored within UAE borders under ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139). Direct Billing Verification available via WhatsApp +971 54 548 8731.
Clinical & Logistical Metadata
| Test Name | Whole Exome + Mitochondrial Genome Sequencing |
| Price (AED) | 7,000 AED |
| Turnaround Time | 3–4 Weeks |
| Sample Type / Matrix | Whole Blood (Peripheral Blood) – VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM) |
| Methodology Used | Next-Generation Sequencing (NGS) with Proprietary Enrichment and Deep Sequencing |
| ICD-10-CM Code | Z01.5, R69 |
| LOINC Code | 81237-6 |
| DHA Facility License & Laboratory Address | DHA Facility License Number: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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ISMS 27001:2022
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All reports reviewed by DHA-Certified physicians