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.

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781

Listed price range

550.00–150,000.00 AED

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Molecular Diagnostics test prices

Showing 586–600 of 781 matching tests.

Molecular Diagnostics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3980 Pancreatitis Panel Genetic Test This test evaluates genetic variants in 28 genes associated with an increased risk of developing hereditary pancreatitis and pancreatic cancer.	Peripheral Whole Blood – 2 mL in EDTA Tube	21–28 Days (3–4 Weeks)	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in 28 genes (PRSS1, SPINK1, CFTR, CTRC, etc.)", "Genetic predisposition to pancreatitis and pancreatic cancer"] Parameters [] Preparation ["No specific fasting required", "Continue all prescribed medications"] Indications ["Individuals with chronic or recurrent pancreatitis", "Individuals with a family history of pancreatic cancer", "Suspected hereditary pancreatitis syndromes"] Measurement technique Confirm with laboratory Codes LOINC: 94227-4 ICD-10: K86.1, Z15.09 Clinical summary This test evaluates genetic variants in 28 genes associated with an increased risk of developing hereditary pancreatitis and pancreatic cancer.
TEST-352 Papaya GMO Testing Test This test detects genetically modified DNA from ingested papaya in circulating white blood cells.	Whole Blood (Peripheral)	5 business days	1,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Genetically modified DNA sequences from papaya", "Circulating leukocyte DNA"] Parameters [] Preparation ["No fasting required for this test alone.", "Maintain normal food intake for true exposure reflection.", "No specific dietary restrictions are required."] Indications ["Assessment of dietary exposure to GMO papaya", "Personalized nutritional strategies"] Measurement technique Confirm with laboratory Codes LOINC: 58448-7 ICD-10: Z13.9, Z71.3 Clinical summary This test detects genetically modified DNA from ingested papaya in circulating white blood cells.
TEST-3718 Parkinson Disease NGS Genetic Panel Test This test evaluates for pathogenic variants in multiple genes associated with hereditary Parkinson's disease.	Peripheral whole blood (3-5 mL EDTA)	3-4 Weeks	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in >30 genes (SNCA, LRRK2, PARK2, PINK1, DJ-1, etc.)", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)", "Copy Number Variants (CNVs)"] Parameters [] Preparation [] Indications ["Individuals with a family history of Parkinson’s disease", "Individuals with early-onset Parkinson’s symptoms", "Family screening for at-risk relatives"] Measurement technique Confirm with laboratory Codes LOINC: 83440-6 ICD-10: G20 Clinical summary This test evaluates for pathogenic variants in multiple genes associated with hereditary Parkinson's disease.
TEST-674 Parvovirus B19 DNA Detection (Qualitative) Test This test detects the presence of parvovirus B19 DNA in a respiratory sample, indicating an active infection.	Respiratory secretion (nasopharyngeal swab)	36 to 48 hours	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Viral DNA", "Active viral shedding"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any relevant medical history"] Indications ["Suspected active parvovirus B19 infection", "Evaluation of pregnant patients with potential exposure", "Assessment of immunocompromised individuals", "Diagnosis in cases of unexplained anemia or rash"] Measurement technique Confirm with laboratory Codes LOINC: 25998-7 ICD-10: B08.3, B97.6 Clinical summary This test detects the presence of parvovirus B19 DNA in a respiratory sample, indicating an active infection.
TEST-1246 Parvovirus B19 Qualitative PCR Test This test detects the presence of Parvovirus B19 DNA in blood or CSF, indicating an active infection.	Whole blood or cerebrospinal fluid (CSF)	2–3 business days	650.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Parvovirus B19 DNA presence"] Parameters [] Preparation ["No special preparation needed", "Inform physician about symptoms or recent exposures", "Follow hospital instructions for CSF collection"] Indications ["Suspected acute Parvovirus B19 infection", "Diagnosis in immunocompromised patients", "Diagnosis in pregnant women", "Diagnosis in patients with neurological symptoms"] Measurement technique Confirm with laboratory Codes LOINC: 29550-4 ICD-10: B08.3 Clinical summary This test detects the presence of Parvovirus B19 DNA in blood or CSF, indicating an active infection.
TEST-545 Paternal Lineage Y-STR Test This test analyzes Y-chromosome STR markers to determine biological paternal relationships.	Buccal Cheek Swab or Peripheral Blood	10 working days	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["27 Y-STR loci", "Allele calls", "Statistical likelihood ratios"] Parameters [] Preparation ["No preparation required for buccal swab collection", "Inform phlebotomist of anticoagulant therapy or bleeding disorder if blood draw is elected"] Indications ["Establishing or excluding patrilineal relationships", "Personal ancestry tracing", "Family verification", "Legal documentation requiring genetic evidence"] Measurement technique Confirm with laboratory Codes LOINC: 76375-7 ICD-10: Z13.89 Clinical summary This test analyzes Y-chromosome STR markers to determine biological paternal relationships.
TEST-2695 Paternal UPD Chromosome 14 (Kagami‑Ogata Syndrome) Genetic Test This test identifies paternal uniparental disomy of chromosome 14, confirming Kagami-Ogata syndrome.	Whole Blood (FTA Card or Venipuncture)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Paternal Uniparental Disomy (UPD) of Chromosome 14"] Parameters [] Preparation ["No fasting required"] Indications ["Suspected Kagami-Ogata syndrome", "Neonates and children with characteristic features"] Measurement technique Confirm with laboratory Codes LOINC: 94493-2 ICD-10: Q99.8, Q87.19, Z13.79 Clinical summary This test identifies paternal uniparental disomy of chromosome 14, confirming Kagami-Ogata syndrome.
TEST-419 Paternity DNA Test (Blood & Products of Conception) This diagnostic test evaluates genetic markers to determine biological parentage.	Whole blood, extracted DNA, or Products of Conception (POC)	5–7 working days	7,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Short Tandem Repeats (STR) markers", "Amelogenin gene"] Parameters [] Preparation ["No dietary restrictions or medication changes are required.", "Avoid applying creams or lotions to the skin on the day of collection.", "Inform the phlebotomist of any recent blood transfusions or medical treatments."] Indications ["Legal determination of paternity", "Immigration purposes", "Custody proceedings", "Inheritance claims"] Measurement technique Confirm with laboratory Codes LOINC: 21635-8 ICD-10: Z04.8 Clinical summary This diagnostic test evaluates genetic markers to determine biological parentage.
TEST-3856 PAX2 Gene Focal Segmental Glomerulosclerosis Type 7 Genetic Test This genetic test identifies pathogenic variants in the PAX2 gene associated with hereditary Focal Segmental Glomerulosclerosis Type 7.	Whole Blood (EDTA), Extracted DNA, 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 ["PAX2 gene pathogenic variants", "Single-nucleotide variants (SNVs)", "Insertions/Deletions (Indels)", "Exon-level copy-number variations (CNVs)"] Parameters [] Preparation ["Do not discontinue prescribed medications", "Postpone collection for two weeks following febrile illness, major trauma, or surgery"] Indications ["Confirming diagnosis of hereditary FSGS type 7", "Guiding family screening", "Informing renal-replacement planning"] Measurement technique Confirm with laboratory Codes LOINC: 90546-3 ICD-10: N04.1 Clinical summary This genetic test identifies pathogenic variants in the PAX2 gene associated with hereditary Focal Segmental Glomerulosclerosis Type 7.
TEST-6015 PAX4 Gene Maturity-Onset Diabetes of the Young Type 9 (MODY9) Genetic Test This genetic test identifies mutations in the PAX4 gene associated with Maturity-Onset Diabetes of the Young Type 9 (MODY9). It helps confirm the diagnosis in individuals with susp...	Peripheral Blood (Whole Blood in EDTA or FTA Card)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PAX4 gene mutations", "Genetic variants associated with MODY9"] Parameters [] Preparation ["No fasting required", "Pre-test genetic counseling is required"] Indications ["Suspected monogenic diabetes", "Atypical diabetes presentation", "Family history of MODY9"] Measurement technique Confirm with laboratory Codes LOINC: 21649-0 ICD-10: E13.0 Clinical summary This genetic test identifies mutations in the PAX4 gene associated with Maturity-Onset Diabetes of the Young Type 9 (MODY9). It helps confirm the diagnosis in individuals with suspected monogenic diabetes.
TEST-3577 PDE6C Cone-Rod Dystrophy Type 4 Genetic Test This genetic test analyzes the PDE6C gene for mutations associated with autosomal recessive cone-rod dystrophy type 4.	Whole Blood (Peripheral Venous)	3 – 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PDE6C gene mutations", "Pathogenic variants"] Parameters [] Preparation [] Indications ["Suspected cone-rod dystrophy type 4", "Family history of inherited retinal dystrophy"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: H35.54 Clinical summary This genetic test analyzes the PDE6C gene for mutations associated with autosomal recessive cone-rod dystrophy type 4.
TEST-1243 PDGFR & cKIT Gene Mutation Analysis (GIST) Test This test identifies mutations in the PDGFRA and KIT genes within tumor tissue to guide GIST therapy.	Archival Tissue Specimen (FFPE Block or Biopsy Slides)	7–8 business days	2,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PDGFRA gene mutations (exons 12, 14, 18)", "KIT gene mutations (exons 9, 11, 13, 17)"] Parameters [] Preparation ["No fasting required", "No medication discontinuation needed", "Valid physician prescription is mandatory"] Indications ["Diagnosis of Gastrointestinal Stromal Tumors (GIST)", "Guidance for imatinib therapy in GIST", "Identification of alternative therapeutic pathways in wild-type GIST"] Measurement technique Confirm with laboratory Codes LOINC: 92856-4 ICD-10: C49.A Clinical summary This test identifies mutations in the PDGFRA and KIT genes within tumor tissue to guide GIST therapy.
TEST-1254 PDGFR Mutation Screening (Exons 12, 14, 18) Test This test detects activating mutations in the PDGFRA gene exons 12, 14, and 18, which are key drivers in certain GIST cases.	Archival Tissue Specimen — Formalin-Fixed Paraffin-Embedded (FFPE) Block or Fresh Frozen Tumor Tissue	7–8 Working Days	1,600.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PDGFRA gene mutations", "Activating mutations in exons 12, 14, 18"] Parameters [{"name": "Analytical Precision", "reference_range": ">99.9% per-base accuracy; bidirectional exon coverage"}] Preparation ["Valid doctor's prescription required", "Original histopathology report required"] Indications ["Diagnosis of GIST", "KIT-wildtype GIST", "Guidance for targeted therapy selection"] Measurement technique Confirm with laboratory Codes LOINC: 92105-9 ICD-10: Z13.89 Clinical summary This test detects activating mutations in the PDGFRA gene exons 12, 14, and 18, which are key drivers in certain GIST cases.
TEST-3204 PDGFRB Gene Myeloproliferative Disorder, Chronic, with Eosinophilia Genetic Test This test evaluates the PDGFRB gene for mutations associated with chronic eosinophilia and myeloproliferative disorders.	Peripheral Whole Blood (Venous Blood Draw or FTA Card)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PDGFRB gene mutations (point mutations, insertions, deletions, copy-number changes)", "Genetic variants within the PDGFRB gene"] Parameters [] Preparation [] Indications ["Diagnosis of myeloproliferative disorder with chronic eosinophilia", "Guiding targeted therapy selection (e.g., imatinib)"] Measurement technique Confirm with laboratory Codes LOINC: 92819-5 ICD-10: D47.1 Clinical summary This test evaluates the PDGFRB gene for mutations associated with chronic eosinophilia and myeloproliferative disorders.
TEST-1239 PDGFRβ (CMML) Gene Rearrangement Test This diagnostic test evaluates for rearrangements in the PDGFRβ gene, a key marker for Chronic Myelomonocytic Leukemia (CMML).	Bone Marrow Aspirate or Peripheral Blood (EDTA)	3–4 days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PDGFRβ gene rearrangement", "Chromosome 5q32-33 alterations"] Parameters [] Preparation ["Fasting is not required.", "No specific medication or diet restrictions."] Indications ["Diagnosis of Chronic Myelomonocytic Leukemia (CMML)", "Prognosis assessment in CMML", "Prediction of response to tyrosine kinase inhibitors (e.g., imatinib)"] Measurement technique Confirm with laboratory Codes LOINC: 92847-3 ICD-10: C93.1 Clinical summary This diagnostic test evaluates for rearrangements in the PDGFRβ gene, a key marker for Chronic Myelomonocytic Leukemia (CMML).

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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Molecular Diagnostics tests in Dubai & UAE

Molecular Diagnostics test prices

Molecular Diagnostics: overview

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