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 46–60 of 781 matching tests.

Molecular Diagnostics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5019 APCDD1 Gene Hypotrichosis Type 1 Genetic Test This test analyzes the APCDD1 gene to detect pathogenic mutations associated with hereditary hypotrichosis simplex type 1.	Peripheral whole blood (3–5 mL) or dried blood spot on FTA card	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["APCDD1 gene mutations", "Copy Number Variants (CNVs) in APCDD1"] Parameters [] Preparation [] Indications ["Diagnosis of hereditary hypotrichosis simplex type 1", "Carrier testing in at-risk relatives"] Measurement technique Confirm with laboratory Codes LOINC: 94027-0 ICD-10: Q84.0 Clinical summary This test analyzes the APCDD1 gene to detect pathogenic mutations associated with hereditary hypotrichosis simplex type 1.
TEST-6245 APOA5 Gene Hyperchylomicronemia Type 5 Genetic Test This test identifies genetic mutations in the APOA5 gene associated with hyperchylomicronemia type 5, a severe lipid disorder.	Peripheral whole blood (EDTA tube), extracted DNA, or FTA card	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the APOA5 gene"] Parameters [] Preparation ["Fasting is not required", "Inform phlebotomist of all medications and supplements"] Indications ["Unexplained severe hypertriglyceridemia", "Recurrent pancreatitis", "Family history suggestive of familial hyperchylomicronemia"] Measurement technique Confirm with laboratory Codes LOINC: 81293-3 ICD-10: E78.3 Clinical summary This test identifies genetic mutations in the APOA5 gene associated with hyperchylomicronemia type 5, a severe lipid disorder.
TEST-6187 APOB Gene Hypobetalipoproteinemia Type 1 Genetic Test This genetic test identifies pathogenic variants in the APOB gene associated with familial hypobetalipoproteinemia type 1.	Whole Blood, Extracted DNA, or FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the APOB gene", "Lipid metabolism disorder risk"] Parameters [] Preparation ["No fasting required", "Genetic counselling session required before testing"] Indications ["Suspected familial hypobetalipoproteinemia type 1", "Family history of the disorder", "Evaluation of lipid metabolism disorders"] Measurement technique Confirm with laboratory Codes LOINC: 94821-7 ICD-10: E78.6, Z83.49, E88.9 Clinical summary This genetic test identifies pathogenic variants in the APOB gene associated with familial hypobetalipoproteinemia type 1.
TEST-6004 APOC2 Gene Apolipoprotein C-II Deficiency Genetic Test This genetic test identifies pathogenic variants in the APOC2 gene associated with Apolipoprotein C-II deficiency.	Peripheral Whole Blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["APOC2 gene variants", "Pathogenic mutations"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any current medications"] Indications ["Diagnosis of Apolipoprotein C-II deficiency", "Family cascade screening", "Differentiation from other hyperlipidemias"] Measurement technique Confirm with laboratory Codes LOINC: 48767-8 ICD-10: E78.1 Clinical summary This genetic test identifies pathogenic variants in the APOC2 gene associated with Apolipoprotein C-II deficiency.
TEST-3819 APOL1 Gene Susceptibility to Focal Segmental Glomerulosclerosis Type 4 (FSGS4) Test This genetic test identifies APOL1 risk variants (G1 and G2) associated with increased susceptibility to FSGS4 and end-stage kidney disease.	Peripheral whole blood (EDTA tube)	3–4 Weeks (includes post-test genetic counselling)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["APOL1 gene variants (G1 and G2)", "Genetic risk for FSGS4"] Parameters [] Preparation ["No specific fasting required", "Avoid testing during acute febrile illness"] Indications ["Individuals of African ancestry with proteinuria", "Unexplained CKD", "Family history of FSGS", "Collapsing glomerulopathy", "HIV-associated nephropathy", "Evaluation for kidney transplantation"] Measurement technique Confirm with laboratory Codes LOINC: 81968-6 ICD-10: Z15.89, N04.1, Z84.1 Clinical summary This genetic test identifies APOL1 risk variants (G1 and G2) associated with increased susceptibility to FSGS4 and end-stage kidney disease.
TEST-6062 APRT Gene Adenine Phosphoribosyltransferase Deficiency Genetic Test This genetic test detects pathogenic variants in the APRT gene responsible for adenine phosphoribosyltransferase deficiency.	Whole Blood, FTA Card Spot, or Previously Extracted DNA	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the APRT gene", "Single nucleotide variants", "Small insertions", "Small deletions"] Parameters [] Preparation ["No fasting required", "Genetic counselling session mandatory before testing"] Indications ["Suspected adenine phosphoribosyltransferase deficiency", "Recurrent 2,8-dihydroxyadenine kidney stones", "Chronic kidney disease of unknown origin"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: E79.8 Clinical summary This genetic test detects pathogenic variants in the APRT gene responsible for adenine phosphoribosyltransferase deficiency.
TEST-269 Aptamer Sequencing and Analysis Test This test profiles synthetic aptamer libraries to identify high-affinity biomarkers relevant to oncology, rheumatology, and precision medicine.	Whole Blood (Peripheral)	8 weeks	4,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["High-affinity biomarkers", "Synthetic oligonucleotide aptamer libraries"] Parameters [] Preparation ["Do not discontinue prescribed medication without consulting your doctor."] Indications ["Oncology biomarker discovery", "Rheumatology biomarker discovery", "Precision medicine applications"] Measurement technique Confirm with laboratory Codes LOINC: 51961-4 ICD-10: Z12.9 Clinical summary This test profiles synthetic aptamer libraries to identify high-affinity biomarkers relevant to oncology, rheumatology, and precision medicine.
TEST-3928 AR Gene Androgen Insensitivity Genetic Test This test evaluates the androgen receptor (AR) gene for mutations associated with androgen insensitivity syndrome (AIS). It identifies variants causing complete, partial, or mild f...	Whole Blood, Extracted DNA, or Dried Blood Spot (FTA Card)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Mutations in the AR gene", "Point mutations", "Copy number variations"] Parameters [] Preparation ["Provide a complete medication list at the time of sample collection.", "Do not discontinue or alter any prescribed medication without consulting your referring physician."] Indications ["Diagnosis of Androgen Insensitivity Syndrome (AIS)", "Family planning for individuals with AIS", "Evaluation of ambiguous genitalia", "Investigation of infertility"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: E34.5 Clinical summary This test evaluates the androgen receptor (AR) gene for mutations associated with androgen insensitivity syndrome (AIS). It identifies variants causing complete, partial, or mild forms of AIS.
TEST-150 ATAC Sequencing Data Analysis Test This test evaluates genome-wide open chromatin regions to identify regulatory elements influencing gene expression.	Whole Blood (EDTA) or High-Quality Extracted DNA (>100 ng)	4 Weeks (Guaranteed)	2,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Open chromatin regions", "Regulatory elements (promoters, enhancers)", "Transcription factor binding sites", "Differential accessibility"] Parameters [] Preparation ["No fasting required", "Avoid strenuous exercise for 24 hours before collection", "No medication adjustments unless instructed by physician"] Indications ["Precision oncology", "Rheumatology", "Complex disease research", "Identifying epigenetic drivers"] Measurement technique Confirm with laboratory Codes LOINC: 80462-5 ICD-10: Z01.89 Clinical summary This test evaluates genome-wide open chromatin regions to identify regulatory elements influencing gene expression.
TEST-229 ATAC Sequencing Test This test evaluates genome-wide chromatin accessibility to identify regulatory elements.	Whole Blood (EDTA tube, 2–4 mL) or Extracted Genomic DNA (≥2 µg)	5 weeks	6,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Genome-wide open chromatin regions", "Regulatory elements", "Chromatin accessibility"] Parameters [] Preparation ["No special preparation needed", "Avoid heparin-containing tubes if providing whole blood", "Stay hydrated"] Indications ["Oncology research", "Precision medicine", "Biomarker discovery", "Epigenetic studies"] Measurement technique Confirm with laboratory Codes LOINC: 97926-7 ICD-10: Z01.89 Clinical summary This test evaluates genome-wide chromatin accessibility to identify regulatory elements.
TEST-265 ATAC-Seq Analysis Test This test evaluates genome-wide chromatin accessibility to identify open regulatory regions.	Whole Blood (Peripheral) or Extracted DNA	10 weeks	7,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Genome-wide nucleotide-level chromatin accessibility", "Open chromatin regions", "Active regulatory elements"] Parameters [] Preparation [] Indications ["Oncology research", "Rheumatology research", "Translational research", "Identification of dysregulated chromatin regions in cancer and autoimmune diseases"] Measurement technique Confirm with laboratory Codes LOINC: 94222-8 ICD-10: Z13.9 Clinical summary This test evaluates genome-wide chromatin accessibility to identify open regulatory regions.
TEST-3692 Ataxia Comprehensive Panel Genetic Test This test evaluates for genetic mutations associated with various forms of hereditary ataxia.	Peripheral whole blood	3–4 Weeks	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single nucleotide variants (SNVs)", "Copy number variations (CNVs)"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications without consulting your physician"] Indications ["Patients presenting with progressive imbalance, slurred speech, and coordination difficulties", "Family screening for hereditary ataxia"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: G11.9 Clinical summary This test evaluates for genetic mutations associated with various forms of hereditary ataxia.
TEST-1844 Ataxia Gene Panel Test This test evaluates over 200 genes associated with hereditary ataxias using Next-Generation Sequencing.	Peripheral whole blood or amniotic fluid	4–6 weeks	4,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Genetic variants in over 200 ataxia-associated genes", "Presence of pathogenic mutations"] Parameters [] Preparation ["No drug or dietary supplement avoidance is needed prior to specimen collection."] Indications ["Diagnosis of hereditary ataxia", "Family screening for ataxia risk", "Personalised management planning"] Measurement technique Confirm with laboratory Codes LOINC: 96534-4 ICD-10: G11.9 Clinical summary This test evaluates over 200 genes associated with hereditary ataxias using Next-Generation Sequencing.
TEST-6216 AVPR2 Gene Nephrogenic Diabetes Insipidus, X‑linked Genetic Test This test evaluates the entire coding region of the AVPR2 gene to identify mutations associated with X-linked nephrogenic diabetes insipidus.	Blood (EDTA), FTA Card, or Extracted DNA	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["AVPR2 gene sequence", "Single nucleotide variants", "Insertions", "Deletions", "Copy number changes"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication (e.g., thiazides, amiloride) without consulting your doctor."] Indications ["Suspected X-linked nephrogenic diabetes insipidus", "Differentiation from central diabetes insipidus", "Guiding treatment planning", "Family planning"] Measurement technique Confirm with laboratory Codes LOINC: 81267-8 ICD-10: N25.1, Z13.79, Z84.89 Clinical summary This test evaluates the entire coding region of the AVPR2 gene to identify mutations associated with X-linked nephrogenic diabetes insipidus.
TEST-542 Avuncular (Aunt/Uncle) DNA Relationship Test This test evaluates the statistical probability of a biological aunt/uncle relationship using STR analysis.	Peripheral whole blood (EDTA tube) or buccal swab	10 Working Days (Expedited 7-day option available)	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Combined Relationship Index (CRI)", "Autosomal STR loci (21-27)", "Amelogenin markers"] Parameters [{"name": "Combined Relationship Index (CRI)", "reference_range": "≥ 10,000:1 (Inclusion); < 0.001 (Exclusion)"}] Preparation ["No specific fasting required", "Inform healthcare provider of recent blood transfusions or bone marrow transplants"] Indications ["Establishing aunt/uncle relationship when parentage testing is unavailable", "Legal matters involving kinship", "Inheritance disputes", "Personal confirmation of relationship"] Measurement technique Confirm with laboratory Codes LOINC: 92804-3 ICD-10: Z13.79 Clinical summary This test evaluates the statistical probability of a biological aunt/uncle relationship using STR analysis.

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.

Before booking

Use the test details as a conversation starter

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.

Explore this area

Molecular Diagnostics tests in Dubai & UAE

Molecular Diagnostics test prices

Molecular Diagnostics: overview

Use the test details as a conversation starter

Related Molecular Diagnostics categories