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Test Price

2,000 AED

✅ Home Collection Available

Sanger Sequencing (Single Variant) – Precision Genetic Confirmation

Executive Summary & Core Metrics

Executive Summary

Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).

Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection, available daily from 8 AM to 11 PM.

Clinical Guidance: Post-test telephonic consultation by a DHA-licensed genetics specialist for result interpretation and family risk counselling.

Insurance: Direct Billing Verification via WhatsApp: +971 54 548 8731.

Test Overview & Methodology

Sanger sequencing, the gold-standard method for confirming single nucleotide variants and small insertions/deletions, precisely identifies a specific familial or suspected mutation. This test is mandated for carrier screening, pre-marital genetic counselling, and paediatric diagnostic workups under DHA guidelines. The assay uses bidirectional sequencing to achieve >99.9% analytical accuracy, ensuring reliable confirmation of known or suspected pathogenic variants.

Feature Our Test (Sanger Single Variant) Closest Alternative (NGS Panel)
Precision 99.9% for targeted variant High breadth, lower depth at single locus
Method Gold-standard bidirectional Sanger Massively parallel sequencing (NGS)
Speed Report in 30 working days Often 2–4 weeks, may miss low-frequency variants

Physician Insight & Safety Protocols

“A single-variant result is only meaningful when correlated with clinical phenotype and family history. This test confirms a specific mutation with near-absolute certainty but cannot exclude other genetic aetiologies; follow-up genetic counselling remains essential, especially for paediatric patients in the UAE where consanguinity elevates autosomal recessive risk. The patient’s full clinical picture, including ancestry and inheritance patterns, must guide interpretation.”

— Lina Osama Zaki Quteineh, Consultant Medical Genetics (DHA License: 9294403)

Important Medication Advisory

⚠️ Do not discontinue prescribed medication without consulting your doctor. Genetic test results may influence treatment decisions, but any changes must be made under medical supervision.

Exclusion Criteria & Emergency Red Flags

  • Not designed for emergency diagnosis; do not delay acute care awaiting results.
  • Not suitable as a stand-alone screen for diseases caused by multiple genes or large chromosomal rearrangements.
  • Emergency Red Flags: If the patient (especially a child) develops seizures, loss of consciousness, respiratory distress, or sudden deterioration, seek hospital emergency care immediately.

Patient FAQ & Clinical Guidance

1. What is the accuracy of Sanger sequencing for detecting a single variant?

Sanger sequencing achieves >99.9% analytical accuracy for known single nucleotide variants, making it the international gold standard for confirmation. This high fidelity is maintained through bidirectional reads and ISO‑certified workflows at our UAE facility.

2. What is the turnaround time for results?

Your comprehensive report is delivered within 30 working days from sample receipt, allowing meticulous bidirectional sequencing and clinical interpretation by DHA‑licensed specialists.

3. Is this test covered by insurance in the UAE?

We verify direct billing eligibility with all major UAE insurers instantly via WhatsApp at +971 54 548 8731; many comprehensive policies cover single‑variant testing when medically indicated.

UAE Regulatory & Data Privacy Adherence

Compliance Framework: This service adheres to 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. Processing is performed under DHA/MOHAP standard nomenclature and ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139). All staff hold valid DHA licences. Patient consent and medical liability are governed by Federal Decree‑Law No. 4 of 2016 on Medical Liability.

Clinical & Logistical Metadata

Test Name Sanger Sequencing (Single Variant)
Price (AED) 2,000
Turnaround Time 30 Working Days
Sample Type / Matrix Peripheral Whole Blood
Methodology Used Bidirectional Sanger Sequencing
ICD-10-CM Code Z13.79
LOINC Code 55233-1
DHA Facility License & Laboratory Address License: 1143 – Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE

Corporate Lab: DNA Labs UAE

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All reports reviewed by DHA-Certified physicians