Diagnostic options · 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 706–720 of 781 matching tests.
| Test and description | Specimen | Typical duration | Price | Options |
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TEST-3152
Spinal Muscular Atrophy (SMA) Carrier Detection Test
This test evaluates an individual's carrier status for Spinal Muscular Atrophy (SMA) by analyzing the SMN1 gene. |
Whole blood (EDTA lavender top) | 5 business days (sample collected Monday by 11 AM, report by Saturday) | 2,000.00 AED | |
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TEST-3159
Spinal Muscular Atrophy (SMA) Mutation Detection Test
This test detects deletions and copy number variations in the SMN1 gene, the primary cause of Spinal Muscular Atrophy (SMA). It is used for diagnosis and carrier screening. |
Peripheral Whole Blood (Lavender-top EDTA Tube) | 6 business days (sample submission Monday by 11 AM → report Saturday) | 2,000.00 AED | |
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TEST-3085
Spinocerebellar Ataxia (SCA) Comprehensive Profile Test
This test evaluates for pathogenic trinucleotide repeat expansions and mutations in genes linked to multiple types of Spinocerebellar Ataxia (SCA) and DRPLA. |
Peripheral whole blood | 5–7 business days from sample receipt | 1,800.00 AED | |
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TEST-3058
Spinocerebellar Ataxia (SCA) Extended Profile Test
This genetic test identifies pathogenic trinucleotide repeat expansions in multiple genes associated with Spinocerebellar Ataxia (SCA). It provides a definitive molecular diagnosis... |
4 mL EDTA Whole Blood (Lavender-top tube) | 5 working days | 4,500.00 AED | |
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TEST-3054
Spinocerebellar Ataxia (SCA) Genetic Profile (4 Markers) Test
This test identifies pathogenic trinucleotide repeat expansions in the SCA1, SCA2, SCA3, and SCA6 genes, which are common causes of autosomal dominant cerebellar ataxia. |
Peripheral Whole Blood (EDTA) | Report by Saturday (sample received by Tuesday 11:00 AM) | 1,500.00 AED | |
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TEST-1102
Spinocerebellar Ataxia (SCA) Test
This test identifies specific genetic mutations associated with Spinocerebellar Ataxia (SCA) in a peripheral blood sample. |
Peripheral whole blood (EDTA tube) | 5–7 working days | 700.00 AED | |
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TEST-3194
SPTA1 Gene Spherocytosis Type 3 Genetic Test
This genetic test evaluates the SPTA1 gene for pathogenic variants associated with hereditary spherocytosis type 3. |
Peripheral Whole Blood (3-5 mL EDTA) or Buccal Swab | 3–4 Weeks | 2,800.00 AED | |
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TEST-348
Squash/Zucchini GMO Testing Test
This diagnostic test evaluates the presence of genetically modified DNA sequences in squash or zucchini food samples. |
Food sample (squash or zucchini) | 1 Week | 1,000.00 AED | |
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TEST-5353
SRGAP2 Gene Neuronal Migration Disorder Genetic Test
This genetic test evaluates the SRGAP2 gene for variants associated with neuronal migration disorders. |
Peripheral whole blood (venous or capillary) or FTA card | 3–4 weeks | 2,800.00 AED | |
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TEST-1233
SRY Gene FISH Test (Y Chromosome Microdeletion)
This test detects the presence or absence of the SRY gene on the Y chromosome using Fluorescence In Situ Hybridization (FISH). It is used to investigate disorders of sexual develop... |
Peripheral whole blood | 4 working days | 1,000.00 AED | |
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TEST-600
Stachybotrys (RNA Detection) Qualitative Test
This test detects the presence of viable RNA from Stachybotrys chartarum, indicating an active infection. |
Tissue, biopsy, respiratory secretions | 36-48 hours | 700.00 AED | |
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TEST-1986
SUFU Gene Meningioma Susceptibility Test (NGS)
This test evaluates the SUFU gene for germline variants associated with an increased risk of developing meningiomas. |
Peripheral Whole Blood (EDTA) or FTA Card | 3 to 4 Weeks | 2,800.00 AED | |
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TEST-351
Sugar Beet GMO Detection Test (PCR)
This test detects and quantifies genetically modified sugar beet DNA sequences in whole blood using multiplex Real-Time PCR (qPCR) / Digital Droplet PCR. |
Whole Blood (Peripheral Venipuncture) | 5–7 Business Days | 1,000.00 AED | |
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TEST-61
T‑Cell Gene Rearrangement Mutation Detection Test
This test identifies clonal expansions of T-cells by detecting unique rearrangements in T-cell receptor genes using multiplex PCR and fragment analysis. |
Peripheral whole blood (EDTA) | 15 working days | 2,500.00 AED | |
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TEST-3207
t(12;21)(p13;q22) ETV6-RUNX1 (TEL-AML1) PCR Qualitative Test
This test detects the ETV6-RUNX1 gene fusion, a key marker for risk stratification in childhood B-cell acute lymphoblastic leukemia. |
Bone Marrow Aspirate or EDTA Whole Blood | 3 Working Days | 650.00 AED | |
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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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