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

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Molecular Diagnostics test prices

Showing 631–645 of 781 matching tests.

Molecular Diagnostics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-6397 PSAP Gene Genetic Test for Atypical Gaucher Disease (NGS) This test evaluates the PSAP gene for pathogenic variants associated with atypical Gaucher disease (saposin C deficiency).	Peripheral whole blood (3–5 mL in EDTA) or buccal swab	21–28 business days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the PSAP gene", "Single-nucleotide resolution analysis"] Parameters [] Preparation ["No fasting required", "Mandatory pre-test genetic counselling session"] Indications ["Suspected atypical Gaucher disease", "Family history of Gaucher disease", "Carrier screening", "Prenatal diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: E75.22 Clinical summary This test evaluates the PSAP gene for pathogenic variants associated with atypical Gaucher disease (saposin C deficiency).
TEST-3753 PSEN1 Gene Alzheimer Disease Type 3 Genetic Test This test identifies pathogenic variants in the PSEN1 gene associated with early-onset familial Alzheimer disease type 3.	Whole Blood (EDTA), DNA Extract, or FTA Card Dried Blood Spot	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 PSEN1 gene"] Parameters [] Preparation [] Indications ["Individuals with a strong family history of early-onset Alzheimer disease type 3", "Genetic counselling for families with suspected hereditary Alzheimer's disease"] Measurement technique Confirm with laboratory Codes LOINC: 94291-1 ICD-10: G30.0 Clinical summary This test identifies pathogenic variants in the PSEN1 gene associated with early-onset familial Alzheimer disease type 3.
TEST-3775 PSEN2 Gene Alzheimer Disease Type 4 (AD4) Genetic Test This test evaluates the PSEN2 gene for pathogenic variants associated with early-onset familial Alzheimer disease type 4 (AD4).	Whole blood (EDTA) – 3–5 mL	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 PSEN2 gene", "Single nucleotide variants", "Small insertions/deletions", "Copy-number variations"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications without consulting your physician"] Indications ["Individuals with a strong family history of early-onset dementia", "Proactive neurological and anti-aging risk assessment", "Predictive testing for asymptomatic adults with a known family mutation"] Measurement technique Confirm with laboratory Codes LOINC: 93935-7 ICD-10: G30.0, G30.9 Clinical summary This test evaluates the PSEN2 gene for pathogenic variants associated with early-onset familial Alzheimer disease type 4 (AD4).
TEST-2016 PTPN11 Gene Juvenile Myelomonocytic Leukemia (JMML) Genetic Test This test identifies pathogenic variants in the PTPN11 gene associated with JMML and Noonan syndrome.	Peripheral Whole Blood	3–4 Weeks (including genetic counselling)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PTPN11 gene pathogenic variants", "JMML-associated mutations"] Parameters [] Preparation ["Pre-test genetic counselling is mandatory", "Provide pedigree chart and clinical history"] Indications ["Suspected diagnosis of Juvenile Myelomonocytic Leukemia (JMML)", "Evaluation for Noonan syndrome spectrum disorders", "Family history of JMML or Noonan syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 69548-0 ICD-10: C93.3, Q87.19, Z15.09 Clinical summary This test identifies pathogenic variants in the PTPN11 gene associated with JMML and Noonan syndrome.
TEST-5788 PTPN23 Gene Ciliogenesis‑Related Disorder NGS Test This test evaluates the PTPN23 gene for pathogenic variants associated with ciliogenesis-related disorders.	Whole Blood (EDTA) or FTA card dried blood spot	3–4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PTPN23 gene sequence", "Single nucleotide variants", "Small insertions and deletions", "Copy number alterations"] Parameters [] Preparation ["Mandatory pre-test genetic counselling", "Provide three-generation family history", "No fasting required", "Bring list of current medications"] Indications ["Suspected ciliopathy", "Recurrent otitis media", "Chronic rhinosinusitis", "Hearing loss"] Measurement technique Confirm with laboratory Codes LOINC: 86200-8 ICD-10: Q87.8, H90.5 Clinical summary This test evaluates the PTPN23 gene for pathogenic variants associated with ciliogenesis-related disorders.
TEST-4558 PTPRC Gene Severe Combined Immunodeficiency (T Cell-Negative, B-Cell/NK-Cell Positive) Genetic Test This genetic test identifies mutations in the PTPRC gene associated with T-cell-negative, B-cell/NK-cell-positive Severe Combined Immunodeficiency (SCID).	Peripheral whole blood, extracted DNA, or FTA card	3–4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PTPRC gene mutations", "Coding exons and splice sites of PTPRC"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any current medications"] Indications ["Suspected Severe Combined Immunodeficiency (SCID)", "Family history of SCID", "Immunological workup suggesting PTPRC-related SCID"] Measurement technique Confirm with laboratory Codes LOINC: 91854-8 ICD-10: D81.2 Clinical summary This genetic test identifies mutations in the PTPRC gene associated with T-cell-negative, B-cell/NK-cell-positive Severe Combined Immunodeficiency (SCID).
TEST-6374 PYGM Gene Glycogen Storage Disease Type 5 Genetic Test This test evaluates the PYGM gene for pathogenic variants associated with Glycogen Storage Disease Type V (McArdle disease). It provides a comprehensive molecular diagnosis using N...	Peripheral Whole Blood (Dried Blood Spot / Venous Draw)	21 Calendar Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PYGM gene pathogenic variants", "Copy Number Variations (CNV) in PYGM gene"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions unless advised by physician"] Indications ["Suspected Glycogen Storage Disease Type V (McArdle disease)", "Family history of McArdle disease", "Unexplained muscle symptoms related to exercise"] Measurement technique Confirm with laboratory Codes LOINC: 83513-6 ICD-10: E74.04 Clinical summary This test evaluates the PYGM gene for pathogenic variants associated with Glycogen Storage Disease Type V (McArdle disease). It provides a comprehensive molecular diagnosis using Next Generation Sequencing (NGS).
TEST-4888 RAB40AL Gene X-Linked Intellectual Disability (XLID) Genetic Test This genetic test evaluates the entire coding region of the RAB40AL gene for pathogenic variants associated with X-linked intellectual disability.	Peripheral whole blood (EDTA, 3–5 mL) or dried blood spot (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 RAB40AL gene", "Copy Number Variants (CNVs) across exons"] Parameters [] Preparation ["No fasting required", "Mandatory pre-test genetic counselling session"] Indications ["Males with unexplained intellectual disability", "Females with family history of XLID seeking carrier status", "Families requiring reproductive planning", "Individuals with clinical features suggestive of XLID"] Measurement technique Confirm with laboratory Codes LOINC: 92880-7 ICD-10: F78, F70, F79 Clinical summary This genetic test evaluates the entire coding region of the RAB40AL gene for pathogenic variants associated with X-linked intellectual disability.
TEST-649 Rabies RNA Qualitative PCR Test This test detects the presence or absence of rabies virus RNA in a saliva sample.	Saliva	7 Business Days	750.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Rabies virus RNA (N gene)", "Rabies virus RNA (L gene)"] Parameters [] Preparation [] Indications ["Suspected rabies exposure", "Post-exposure prophylaxis monitoring"] Measurement technique Confirm with laboratory Codes LOINC: 88575-1 ICD-10: A82.9 Clinical summary This test detects the presence or absence of rabies virus RNA in a saliva sample.
TEST-639 Rabies Viral Load Quantitative Test This test directly detects and quantifies rabies virus RNA in biological samples.	Saliva, Cerebrospinal Fluid (CSF), Tissue, Conjunctival Swab	5–7 business days	750.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Viral RNA (direct pathogen)", "Viral Load"] Parameters [] Preparation ["Sign the informed consent form", "Disclose all current medications", "Avoid rabies immunoglobulin for 24 hours before sample collection", "Inform the clinical team of any bleeding disorders or anticoagulant therapy at least 48 hours before CSF or tissue collection"] Indications ["Known or suspected exposure to rabies virus", "Animal bites", "Occupational contact", "Patients presenting within the incubation window", "Laboratory workers", "Veterinarians", "Wildlife handlers"] Measurement technique Confirm with laboratory Codes LOINC: 88538-3 ICD-10: A82.9 Clinical summary This test directly detects and quantifies rabies virus RNA in biological samples.
TEST-253 Rapid Integrated Clinical Exome (RICE) Sequencing (10X) Test This test evaluates the entire exome and genome structure for clinically actionable variants using 10X linked-read technology.	Peripheral whole blood	5 weeks	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Clinically actionable variants", "Structural variants", "Genome structure"] Parameters [] Preparation ["Avoid food for two hours before blood draw."] Indications ["Oncology", "Anti-aging", "Research", "Identification of disease-causing mutations"] Measurement technique Confirm with laboratory Codes LOINC: 95209-3 ICD-10: Z01.89 Clinical summary This test evaluates the entire exome and genome structure for clinically actionable variants using 10X linked-read technology.
TEST-3585 RAX2 Gene Cone‑Rod Dystrophy Type 11 Genetic Test This test identifies pathogenic variants in the RAX2 gene associated with Cone-Rod Dystrophy Type 11.	Peripheral Whole Blood (EDTA) or Buccal Swab	3–4 Weeks (expedited reporting available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the RAX2 gene", "Single nucleotide variants (SNVs)", "Insertions and deletions (indels)", "Copy number variations (CNVs)"] Parameters [{"name": "Diagnostic Sensitivity", "reference_range": ">99.9% for SNVs, indels, and CNVs"}] Preparation ["No specific fasting required", "Inform lab of any recent blood transfusions"] Indications ["Suspected Cone-Rod Dystrophy Type 11", "Family history of Cone-Rod Dystrophy Type 11", "Genetic counselling for inherited retinal diseases", "Eligibility assessment for gene therapies"] Measurement technique Confirm with laboratory Codes LOINC: 88627-3 ICD-10: H35.52 Clinical summary This test identifies pathogenic variants in the RAX2 gene associated with Cone-Rod Dystrophy Type 11.
TEST-1171 RB1 Gene Deletion & Duplication Detection (Retinoblastoma) Test This test detects large genomic rearrangements (deletions or duplications) within the RB1 gene.	Peripheral whole blood	7–10 working days	1,400.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["RB1 gene deletions", "RB1 gene duplications"] Parameters [] Preparation [] Indications ["Diagnosis of retinoblastoma", "Assessment of familial risk for retinoblastoma", "Identifying at-risk family members"] Measurement technique Confirm with laboratory Codes LOINC: 68956-0 ICD-10: Z13.71 Clinical summary This test detects large genomic rearrangements (deletions or duplications) within the RB1 gene.
TEST-2047 RB1 Gene Hereditary Retinoblastoma Genetic Test This test detects germline mutations in the RB1 gene associated with hereditary retinoblastoma.	Peripheral Whole Blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["RB1 gene mutations", "Germline genetic variants"] Parameters [] Preparation [] Indications ["Family history of retinoblastoma", "Clinical suspicion of retinoblastoma", "Genetic counseling for hereditary cancer risk"] Measurement technique Confirm with laboratory Codes LOINC: 21680-2 ICD-10: C69.20 Clinical summary This test detects germline mutations in the RB1 gene associated with hereditary retinoblastoma.
TEST-2696 RBBP8 Gene (Jawad Syndrome) Genetic Test This test evaluates the RBBP8 gene for pathogenic variants associated with Jawad syndrome.	Whole blood, extracted DNA, or dried blood spot (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 RBBP8 gene", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variants (CNVs)"] Parameters [] Preparation ["No specific fasting required", "Continue all current medications as directed by physician"] Indications ["Suspected Jawad syndrome", "Family history of Jawad syndrome", "Evaluation of neurodevelopmental disorders with characteristic features"] Measurement technique Confirm with laboratory Codes LOINC: 94867-3 ICD-10: Q87.8, Q02, Z15.89 Clinical summary This test evaluates the RBBP8 gene for pathogenic variants associated with Jawad syndrome.

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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