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Diagnostic options Β· UAE

Molecular Diagnostics tests in Dubai & UAE

Compare available Molecular Diagnostics tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

Tests in this category

781

Listed price range

550.00–150,000.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Molecular Diagnostics test prices

Showing 316–330 of 781 matching tests.

Molecular Diagnostics diagnostic tests, details, and listed prices
Test and description Specimen Typical duration Price Options
TEST-4389
GPD1L Gene Brugada Syndrome Type 2 Genetic Test

This genetic test evaluates the GPD1L gene for variants associated with Brugada Syndrome Type 2.

Whole blood (EDTA), extracted genomic DNA, or FTA card blood spot 3–4 weeks (expedited: 10 working days) 2,800.00 AED
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What it measures
["GPD1L gene sequence", "Pathogenic variants in GPD1L"]
Parameters
[]
Preparation
["Do not discontinue antiarrhythmic medication without consulting your cardiologist", "Review medication list with physician"]
Indications
["Diagnosis of Brugada Syndrome Type 2", "Risk stratification for sudden cardiac death", "Family screening for BrS2"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 82176-6 ICD-10: I45.81
Clinical summary
This genetic test evaluates the GPD1L gene for variants associated with Brugada Syndrome Type 2.
TEST-551
Grandparent DNA Test

This test determines the biological relationship between a grandparent and grandchild using DNA analysis.

Buccal swab (preferred), Blood EDTA Tube, DNA FTA Card 10 business days 3,000.00 AED
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What it measures
["Autosomal Short Tandem Repeats (STRs)"]
Parameters
[]
Preparation
["No fasting required", "No medication restrictions", "Avoid blood donation or transfusion for at least four weeks prior"]
Indications
["Establishing biological grandparent-grandchild relationship", "Legal proceedings", "Inheritance disputes", "Personal confirmation"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 37683-0 ICD-10: Z00.8
Clinical summary
This test determines the biological relationship between a grandparent and grandchild using DNA analysis.
TEST-224
Group B Streptococcus (GBS) Library Preparation (NGS) Test

This test sequences the entire GBS genome to identify serotype, virulence factors, and antibiotic resistance genes.

Whole Blood or Pre-extracted DNA (Peripheral Blood) 10 working days from sample receipt 17,500.00 AED
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What it measures
["Serotypes", "Virulence factors", "Antibiotic resistance genes", "Multi-Locus Sequence Typing (MLST)", "Phylogenetic analysis"]
Parameters
[]
Preparation
["No fasting required", "Avoid taking antibiotics for 48 hours before sample collection", "Ensure pre-extracted DNA meets laboratory specifications"]
Indications
["Pregnancy carrier screening", "Epidemiological surveillance", "Vaccine development", "Outbreak investigation", "Maternal-fetal medicine", "Neonatology", "Infectious disease teams", "Public health epidemiology"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 88958-7 ICD-10: Z22.3, B95.1
Clinical summary
This test sequences the entire GBS genome to identify serotype, virulence factors, and antibiotic resistance genes.
TEST-1354
H3N2 & Influenza B Qualitative PCR Test

This diagnostic test evaluates for the presence of genetic material from Influenza A subtype H3N2 and Influenza B viruses.

Buccal Swab or Blood EDTA Same-day reporting when sample is collected by 11:00 AM. 900.00 AED
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What it measures
["Influenza A (H3N2) RNA", "Influenza B RNA"]
Parameters
[]
Preparation
["Avoid eating, drinking, or using mouthwash for 30 minutes prior to buccal swab collection."]
Indications
["Suspected influenza infection", "Diagnosis in high-risk individuals", "Confirmation after negative rapid antigen test", "Epidemiological surveillance"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 92141-3 ICD-10: J10.1
Clinical summary
This diagnostic test evaluates for the presence of genetic material from Influenza A subtype H3N2 and Influenza B viruses.
TEST-822
H9N7 & Influenza A Viral Load Quantitative Test

This test quantifies the viral load of H9N7 and Influenza A RNA in respiratory specimens using PCR and WGS.

Nasopharyngeal swab, throat swab, sputum, or lower respiratory tract specimens. Preliminary results by phone within 36 hours; detailed report on the 4th working day. 1,400.00 AED
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What it measures
["H9N7 viral RNA copies", "Influenza A viral RNA copies", "Genetic subtyping"]
Parameters
[]
Preparation
["No special fasting or fluid restriction required", "Sign consent form", "Provide recent clinical history and medication list", "Bring previous influenza or respiratory panel results", "Avoid mouthwash immediately before sputum sample collection"]
Indications
["Suspected H9N7 infection", "Suspected Influenza A infection", "Monitoring treatment response", "Infection control", "Assessing disease severity"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 85478-4 ICD-10: J09.X2, J09.X9, J10.1
Clinical summary
This test quantifies the viral load of H9N7 and Influenza A RNA in respiratory specimens using PCR and WGS.
TEST-1548
Haemophilia A & B Gene Panel Test

This test evaluates the F8 and F9 genes for pathogenic variants associated with Haemophilia A and B.

Peripheral whole blood 4 – 6 weeks 4,800.00 AED
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What it measures
["Pathogenic variants in F8 gene", "Pathogenic variants in F9 gene", "Copy Number Variations (CNV) in F8/F9 genes"]
Parameters
[]
Preparation
["No fasting required", "Avoid blood transfusions two weeks prior", "Provide a valid doctor’s prescription"]
Indications
["Diagnostic confirmation of haemophilia A or B", "Carrier screening", "Prenatal planning", "Classification of severity"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 90604-7 ICD-10: D66, D67
Clinical summary
This test evaluates the F8 and F9 genes for pathogenic variants associated with Haemophilia A and B.
TEST-1397
Hain’s Mycobacterium Tuberculosis Second-Line Drug Resistance Profile Test

This test detects genetic mutations conferring resistance to second-line anti-tuberculosis drugs using a PCR-based line probe assay.

Sputum, bronchoalveolar lavage (BAL), bronchial aspirate, or cultured growth 5 days (sample cut-off Saturday 11 am, report following Friday) 1,000.00 AED
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What it measures
["Genetic mutations conferring resistance to fluoroquinolones", "Genetic mutations conferring resistance to aminoglycosides", "Genetic mutations conferring resistance to injectable second-line agents (e.g., capreomycin)"]
Parameters
[{"name": "Fluoroquinolones", "reference_range": "Susceptible / Resistant"}, {"name": "Kanamycin", "reference_range": "Susceptible / Resistant"}, {"name": "Amikacin", "reference_range": "Susceptible / Resistant"}, {"name": "Capreomycin", "reference_range": "Susceptible / Resistant"}, {"name": "Ethionamide", "reference_range": "Susceptible / Resistant"}]
Preparation
[]
Indications
["Diagnosis of MDR-TB", "Guidance for second-line TB treatment regimen selection"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 75274-1 ICD-10: Z16.23
Clinical summary
This test detects genetic mutations conferring resistance to second-line anti-tuberculosis drugs using a PCR-based line probe assay.
TEST-6239
HAMP Gene Hemochromatosis Type 2B Genetic Test

This genetic test identifies pathogenic variants in the HAMP gene, which are responsible for Hereditary Hemochromatosis Type 2B.

Peripheral Whole Blood or DNA Sample 3–4 weeks 2,800.00 AED
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What it measures
["Pathogenic variants in the HAMP gene", "Single-nucleotide variants", "Small indels"]
Parameters
[]
Preparation
["No specific fasting required", "Report recent blood transfusions to the laboratory"]
Indications
["Suspected Hereditary Hemochromatosis Type 2B", "Family history of juvenile-onset hemochromatosis", "Evaluation of iron overload disorders"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 87431-6 ICD-10: E83.118
Clinical summary
This genetic test identifies pathogenic variants in the HAMP gene, which are responsible for Hereditary Hemochromatosis Type 2B.
TEST-853
Hantavirus RNA Detection Qualitative Test

This test detects the presence of Hantavirus RNA in patient samples to diagnose acute Hantavirus infections.

Blood, serum, plasma, CSF, bronchial swabs/lavage, urine 24 hours (phone) / 36 hours (email) 1,000.00 AED
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What it measures
["Hantavirus RNA"]
Parameters
[]
Preparation
[]
Indications
["Suspected Hantavirus Pulmonary Syndrome (HPS)", "Suspected Hemorrhagic Fever with Renal Syndrome (HFRS)", "Patients with exposure history and compatible symptoms"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 5402-5 ICD-10: B33.4
Clinical summary
This test detects the presence of Hantavirus RNA in patient samples to diagnose acute Hantavirus infections.
TEST-3186
HBA2 Gene (Alpha Thalassemia) Genetic Test

This test evaluates the HBA2 gene for mutations associated with alpha thalassemia.

Whole Blood (Peripheral), Extracted DNA, or Dried Blood Spot (FTA Card) 3–4 Weeks 2,800.00 AED
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What it measures
["HBA2 gene sequence", "Alpha thalassemia mutations"]
Parameters
[]
Preparation
["Inform geneticist about blood transfusions within the past three months", "Continue prescribed medications unless advised otherwise"]
Indications
["Couples planning a pregnancy", "Individuals presenting with unexplained microcytic anemia", "Individuals with a documented family history of thalassemia"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 21639-0 ICD-10: D56.0
Clinical summary
This test evaluates the HBA2 gene for mutations associated with alpha thalassemia.
TEST-3335
HBB Gene Delta-Beta Thalassemia Genetic Test

This test evaluates the HBB gene for mutations associated with delta-beta thalassemia.

Peripheral whole blood 3 – 4 Weeks (21 – 28 Days) 2,800.00 AED
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What it measures
["Point mutations in HBB gene", "Small insertions/deletions in HBB gene", "Copy number variations in HBB gene"]
Parameters
[]
Preparation
["Mandatory Genetic Counselling & Pedigree Chart"]
Indications
["Diagnosis of delta-beta thalassemia", "Carrier screening", "Prenatal diagnosis", "Family planning", "Confirmation of clinical suspicion"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 79521-2 ICD-10: D56.2
Clinical summary
This test evaluates the HBB gene for mutations associated with delta-beta thalassemia.
TEST-3157
HBD Gene (Delta-Globin) Thalassemia Genetic Test

This test evaluates the HBD gene for mutations associated with delta-beta thalassemia and carrier status.

2 mL Whole Blood (EDTA) / Saliva / FTA Card 3–4 Weeks 2,800.00 AED
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View test specifications and preparation
What it measures
["HBD gene variants", "Single-nucleotide variants", "Small insertions/deletions", "Copy-number alterations"]
Parameters
[]
Preparation
["Inform genetic counsellor of all current medications", "Do not discontinue prescribed medication without consulting physician"]
Indications
["Diagnosis of delta-beta thalassemia", "Carrier status identification", "Evaluation of microcytic anemia"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 104579-2 ICD-10: D56.2
Clinical summary
This test evaluates the HBD gene for mutations associated with delta-beta thalassemia and carrier status.
TEST-1555
HbE (Hemoglobin E) Mutation Screening (Prenatal) Test

This diagnostic test evaluates fetal DNA for the presence of the Hemoglobin E (HbE) mutation.

Fetal DNA (Chorionic Villus, Amniotic Fluid, or Cord Blood) 3-4 Days 800.00 AED
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View test specifications and preparation
What it measures
["Presence of HbE mutation in fetal DNA"]
Parameters
[]
Preparation
[]
Indications
["Prenatal screening for families at risk of hemoglobinopathies", "Couples with known carrier status"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 31208-2 ICD-10: Z31.5, O36.8
Clinical summary
This diagnostic test evaluates fetal DNA for the presence of the Hemoglobin E (HbE) mutation.
TEST-1539
HBOC Extended Panel (32 Genes) Test

This test evaluates 32 genes associated with hereditary breast and ovarian cancer risk using next-generation sequencing.

Peripheral whole blood (EDTA tube) 4–5 weeks from sample receipt 4,800.00 AED
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What it measures
["Pathogenic variants in 32 genes (BRCA1, BRCA2, PALB2, ATM, CHEK2, RAD51C/D, TP53, etc.)", "Lifetime risk stratification for hereditary breast and ovarian cancer"]
Parameters
[]
Preparation
[]
Indications
["Individuals with a strong personal or family history of breast, ovarian, or related cancers.", "Individuals seeking comprehensive hereditary cancer risk assessment.", "Guidance for personalised surveillance or prophylactic strategies."]
Measurement technique
Confirm with laboratory
Codes
LOINC: 81776-9 ICD-10: Z15.01, Z15.02, Z84.81
Clinical summary
This test evaluates 32 genes associated with hereditary breast and ovarian cancer risk using next-generation sequencing.
TEST-4380
HCN4 Gene Brugada Syndrome Type 8 Genetic Test (NGS)

This test identifies pathogenic variants in the HCN4 gene associated with Brugada syndrome type 8.

Whole Blood (EDTA) 3 – 4 Weeks 2,800.00 AED
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View test specifications and preparation
What it measures
["Pathogenic variants in the HCN4 gene"]
Parameters
[]
Preparation
["No special fasting required", "Inform phlebotomist of blood-thinning medications"]
Indications
["Diagnosis of Brugada syndrome type 8", "Risk stratification for ventricular arrhythmias", "Cascade screening for family members"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 94531-1 ICD-10: I49.8
Clinical summary
This test identifies pathogenic variants in the HCN4 gene associated with Brugada syndrome type 8.

Category overview

Molecular Diagnostics: overview

When complex health questions arise, evaluating your health at the cellular level provides the definitive clarity necessary for proactive care. At DNA Labs UAE, our Molecular Diagnostics services harness the power of advanced nucleic acid amplification and real-time PCR technologies to detect diseases with unparalleled sensitivity. From identifying viral loads to pinpointing genetic markers, our specialized molecular testing in the UAE gives your healthcare provider the precise data needed to customize your medical strategy. Trust in one of the leading diagnostic labs in Dubai and the UAE to process your samples with rigorous confidentiality and exceptionally fast, accurate turnaround times. Step forward with absolute confidence. View our molecular diagnostics profiles below, request a seamless home sample collection, or contact our specialized team to book your test.

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The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.

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