Test Price
2,800 AED✅ Home Collection Available
MSH2 Gene Lynch Syndrome (HNPCC) Genetic Test in UAE | 2800 AED
Executive Summary & Core Metrics
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (available daily 8 AM–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 comprehensive Next‑Generation Sequencing test analyzes the entire MSH2 gene for inherited mutations causing Lynch syndrome (hereditary nonpolyposis colorectal cancer type 1), providing lifetime cancer risk stratification and guiding personalized surveillance. The assay includes copy number variation (CNV) detection, achieving a variant detection limit down to 5% allele fraction.
| Feature | Our Test (MSH2 NGS) | Closest Alternative |
|---|---|---|
| Method | NGS – high‑coverage sequencing + CNV analysis | Sanger sequencing (single‑gene) – no CNV detection |
| Detection Limit | Pathogenic variants down to 5% allele fraction | ~15‑20% allele fraction; misses large deletions/duplications |
| Turnaround Time | 3–4 Weeks | 4–6 Weeks (with MLPA add‑on) |
| Clinical Utility | Gold‑standard Lynch syndrome diagnosis per NCCN/ESMO guidelines | Limited to point mutations; inferior risk stratification |
Physician Insight & Safety Protocols
Lina Osama Zaki Quteineh, Consultant Medical Genetics (DHA Registration ID: 9294403) states: “An MSH2 mutation confers a significantly elevated lifetime risk for colorectal and endometrial cancers. This test provides actionable information for surveillance and prophylactic strategies. Always interpret results in the context of personal and family history through a formal genetic counseling session.”
Advisory: Medications and Precautions
Do not discontinue any prescribed medications without consulting your doctor. Inform your physician about all supplements and over‑the‑counter drugs before proceeding with testing.
Exclusion Criteria and Emergency Red Flags
Testing may be deferred if you have received an allogeneic blood transfusion within the last 2 weeks, or are actively undergoing bone marrow or stem cell transplant, as donor DNA may confound germline results. Acute haematological malignancies requiring urgent therapy should be discussed with the ordering physician. Seek immediate medical attention if you experience sudden severe abdominal pain, bright red rectal bleeding, or unexplained weight loss exceeding 5% of body weight in 6 months.
Patient FAQ & Clinical Guidance
1. What is the purpose of the MSH2 Genetic Test?
This test detects pathogenic variants in the MSH2 gene, confirming hereditary colorectal cancer and Lynch syndrome risk. It guides personalized cancer surveillance and preventive measures.
2. How is the sample collected and what preparation is needed?
A simple blood draw (peripheral whole blood) is performed by a certified phlebotomist at your home or in our facility. No special preparation is required. Ensure you are well‑hydrated for easier venous access.
3. How long do results take and will a doctor explain them?
Results are delivered in 3–4 weeks, followed by a complimentary tele‑consultation with a clinical geneticist to interpret findings and discuss next steps.
UAE Regulatory & Data Privacy Adherence
All genetic data is processed and stored in compliance with:
- Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL)
- Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields
- Federal Decree-Law No. 4 of 2016 on Medical Liability
This test is performed by DNA Labs UAE – DHA Facility License Number: 1143. Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE.
Clinical & Logistical Metadata
| Test Name | MSH2 Gene Lynch Syndrome (HNPCC) Genetic Test |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3–4 Weeks |
| Sample Type / Matrix | Peripheral Whole Blood (Standard Phlebotomy) |
| Methodology Used | Next-Generation Sequencing (NGS) with CNV Analysis |
| ICD-10-CM Code | Z15.09, Z80.0 |
| LOINC Code | 35095-5 |
| DHA Facility License & Laboratory Address | License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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