Diagnostic options · UAE

Genetic tests in Dubai & UAE

Compare available Genetic 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

805

Listed price range

600.00–30,000.00 AED

Clinical preparation

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Genetic test prices

Showing 751–765 of 805 matching tests.

Genetic diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-2492 TRPV3 Gene Olmsted Syndrome Genetic Test This diagnostic test evaluates the TRPV3 gene for pathogenic mutations associated with Olmsted syndrome.	Peripheral Whole Blood / Extracted DNA / FTA Card	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic mutations in the TRPV3 gene", "Single nucleotide variants", "Small insertions", "Small deletions"] Parameters [] Preparation ["Mandatory pre-test genetic counselling", "Mandatory pedigree chart completion"] Indications ["Suspected Olmsted syndrome", "Genetic counseling for affected families", "Family cascade screening"] Measurement technique Confirm with laboratory Codes LOINC: 50398-7 ICD-10: Q82.8 Clinical summary This diagnostic test evaluates the TRPV3 gene for pathogenic mutations associated with Olmsted syndrome.
TEST-4071 TRPV4 Gene CMT2C Next-Generation Sequencing (Genetic Test This genetic test evaluates the TRPV4 gene for pathogenic variants associated with Charcot‑Marie‑Tooth disease type 2C.	Whole Blood (Peripheral Venous Blood)	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 TRPV4 gene", "Single-nucleotide variants", "Indels", "Copy-number changes"] Parameters [] Preparation ["No fasting required", "Must attend a genetic counselling session beforehand"] Indications ["Suspected Charcot‑Marie‑Tooth disease type 2C", "Confirmation of molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 81306-1 ICD-10: G60.0 Clinical summary This genetic test evaluates the TRPV4 gene for pathogenic variants associated with Charcot‑Marie‑Tooth disease type 2C.
TEST-5834 TSC1 Gene Tuberous Sclerosis Genetic Test This test sequences the entire TSC1 gene to detect pathogenic variants associated with Tuberous Sclerosis Complex (TSC). It identifies the genetic cause of the disorder in affected...	Whole Blood (3–5 mL in EDTA), Extracted DNA, or Buccal Swab / FTA Card	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TSC1 gene", "Full gene coverage including exons and splice sites"] Parameters [] Preparation ["No fasting required", "Inform phlebotomist if taking anticoagulants"] Indications ["Confirming a genetic diagnosis of Tuberous Sclerosis Complex", "Guiding lifelong surveillance and management", "Genetic counselling for affected families"] Measurement technique Confirm with laboratory Codes LOINC: 82991-3 ICD-10: Q85.1 Clinical summary This test sequences the entire TSC1 gene to detect pathogenic variants associated with Tuberous Sclerosis Complex (TSC). It identifies the genetic cause of the disorder in affected individuals.
TEST-5929 TSC2 Gene (Tuberous Sclerosis Type 2) Genetic Test This test evaluates the TSC2 gene for pathogenic variants associated with Tuberous Sclerosis Complex type 2.	Peripheral whole blood (EDTA)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in TSC2 gene", "Point mutations", "Small indels", "Copy number variations"] Parameters [] Preparation ["Inform genetic counselor about anticoagulant therapy before sample collection"] Indications ["Suspected diagnosis of Tuberous Sclerosis Complex type 2", "Family history of TSC2-related disorders", "Genetic counseling for at-risk individuals"] Measurement technique Confirm with laboratory Codes LOINC: 57937-2 ICD-10: Q85.1 Clinical summary This test evaluates the TSC2 gene for pathogenic variants associated with Tuberous Sclerosis Complex type 2.
TEST-3699 TSHB Gene Sequencing for Congenital Nongoitrous Hypothyroidism Type 4 (Genetic Test) This test identifies genetic mutations in the TSHB gene responsible for congenital nongoitrous hypothyroidism type 4.	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 ["Pathogenic variants in the TSHB gene", "Single-nucleotide variants", "Small insertions/deletions", "Copy-number alterations"] Parameters [] Preparation ["Patients must not discontinue levothyroxine or any thyroid hormone replacement therapy before, during, or after genetic sampling."] Indications ["Confirmed diagnosis of congenital nongoitrous hypothyroidism type 4", "Neonates with abnormal newborn TSH screening but no palpable goitre", "Children with developmental delay and low TSH", "Families with a history of congenital hypothyroidism of unknown genetic origin"] Measurement technique Confirm with laboratory Codes LOINC: 53494-5 ICD-10: E03.1 Clinical summary This test identifies genetic mutations in the TSHB gene responsible for congenital nongoitrous hypothyroidism type 4.
TEST-4104 TSPYL1 Gene Sudden Infant Death with Dysgenesis of the Testes Syndrome Genetic Test This test identifies pathogenic variants in the TSPYL1 gene associated with Sudden Infant Death with Dysgenesis of the Testes Syndrome (SIDDT).	Peripheral whole blood (EDTA), 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 TSPYL1 gene", "Copy Number Variations (CNV) in the TSPYL1 gene"] Parameters [] Preparation ["Pre-test genetic counseling session required", "Do not discontinue prescribed medications"] Indications ["Unexplained infant death", "Infant death with testicular dysgenesis"] Measurement technique Confirm with laboratory Codes LOINC: 29577-1 ICD-10: R95.0, Q55.1 Clinical summary This test identifies pathogenic variants in the TSPYL1 gene associated with Sudden Infant Death with Dysgenesis of the Testes Syndrome (SIDDT).
TEST-2876 TSR2 Gene Sequencing for Diamond-Blackfan Anemia Type 14 with Mandibulofacial Dysostosis Test This diagnostic test evaluates the TSR2 gene for pathogenic variants associated with Diamond-Blackfan anemia type 14 and mandibulofacial dysostosis.	Peripheral blood (5–10 mL) in EDTA tube or 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 TSR2 gene"] Parameters [] Preparation ["No specific fasting required", "No medication modification needed unless instructed by physician"] Indications ["Suspected Diamond-Blackfan anemia type 14", "Suspected mandibulofacial dysostosis", "Genetic counseling for families with affected individuals"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: D61.01, Q75.4 Clinical summary This diagnostic test evaluates the TSR2 gene for pathogenic variants associated with Diamond-Blackfan anemia type 14 and mandibulofacial dysostosis.
TEST-4528 TTC37 Gene Trichohepatoenteric Syndrome Type 1 Genetic Test This test identifies pathogenic variants in the TTC37 gene associated with Trichohepatoenteric syndrome type 1 (THES1).	Peripheral whole blood (3–5 mL in EDTA tube)	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 TTC37 gene", "Full coding region and splice sites of the TTC37 gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of recent blood transfusions"] Indications ["Suspected diagnosis of Trichohepatoenteric syndrome type 1 (THES1)", "Family history of THES1", "Need for precise clinical management and family planning"] Measurement technique Confirm with laboratory Codes LOINC: 81373-8 ICD-10: Q87.8 Clinical summary This test identifies pathogenic variants in the TTC37 gene associated with Trichohepatoenteric syndrome type 1 (THES1).
TEST-4977 TTI2 Gene Sequencing (MRT39) Test This test evaluates the TTI2 gene for pathogenic variants associated with autosomal recessive intellectual disability type 39 (MRT39). It detects single nucleotide variants, small...	Peripheral whole blood (EDTA tube) or buccal swab / saliva (paediatric cases)	3 to 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TTI2 gene coding region", "TTI2 gene intron-exon boundaries", "Copy Number Variations (CNVs) in TTI2 gene"] Parameters [] Preparation ["No specific fasting required", "No specific medication or diet restrictions"] Indications ["Suspected intellectual disability type 39 (MRT39)", "Developmental delay with features suggestive of MRT39"] Measurement technique Confirm with laboratory Codes LOINC: 94218-1 ICD-10: F78 Clinical summary This test evaluates the TTI2 gene for pathogenic variants associated with autosomal recessive intellectual disability type 39 (MRT39). It detects single nucleotide variants, small insertions/deletions, and copy number variations (CNVs) using Next-Generation Sequencing.
TEST-4827 TTN Gene Limb‑Girdle Muscular Dystrophy, Autosomal Recessive Type 2J Genetic Test This test identifies pathogenic variants in the TTN gene associated with Limb-Girdle Muscular Dystrophy Type 2J (LGMD2J).	Whole Blood (EDTA)	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 TTN gene", "Molecular diagnosis of LGMD2J"] Parameters [] Preparation ["No specific fasting required", "Maintain current medication regimen unless advised otherwise by a specialist"] Indications ["Suspected diagnosis of LGMD2J", "Genetic counseling for affected families", "Differential diagnosis of muscular dystrophies"] Measurement technique Confirm with laboratory Codes LOINC: 81308-4 ICD-10: G71.0, Z13.79, Z14.8 Clinical summary This test identifies pathogenic variants in the TTN gene associated with Limb-Girdle Muscular Dystrophy Type 2J (LGMD2J).
TEST-5944 TTPA Gene (Familial Vitamin E Deficiency) Genetic Test This genetic test identifies mutations in the TTPA gene responsible for causing Ataxia with Vitamin E Deficiency (AVED). It provides a definitive molecular diagnosis for patients w...	Peripheral whole blood, venous blood, or FTA blood spot (DNA)	3 to 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic mutations in the TTPA gene", "Coding region and intron-exon boundaries of the TTPA gene"] Parameters [] Preparation ["No specific fasting required", "Continue all prescribed medications unless advised otherwise by your physician"] Indications ["Suspected Ataxia with Vitamin E Deficiency (AVED)", "Family history of AVED", "Unexplained ataxia with low vitamin E levels"] Measurement technique Confirm with laboratory Codes LOINC: 95819-7 ICD-10: E56.0, G11.0 Clinical summary This genetic test identifies mutations in the TTPA gene responsible for causing Ataxia with Vitamin E Deficiency (AVED). It provides a definitive molecular diagnosis for patients with progressive neurological symptoms.
TEST-2413 TUBA8 Gene Polymicrogyria with Optic Nerve Hypoplasia Genetic Test This genetic test analyzes the TUBA8 gene to detect mutations associated with polymicrogyria and optic nerve hypoplasia.	Peripheral Whole Blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TUBA8 gene sequence", "Copy Number Variations (CNVs) in TUBA8"] Parameters [] Preparation ["No specific patient preparation required"] Indications ["Suspected genetic cause of polymicrogyria with optic nerve hypoplasia", "Differential diagnosis of brain malformations"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q04.3, H47.0 Clinical summary This genetic test analyzes the TUBA8 gene to detect mutations associated with polymicrogyria and optic nerve hypoplasia.
TEST-4265 TUBB4A Gene DYT4 Next‑Generation Sequencing Genetic Test This genetic test evaluates the TUBB4A gene for mutations associated with DYT4 dystonia.	Whole Blood or Buccal Swab	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TUBB4A gene sequence", "Pathogenic variants (SNVs, indels, CNVs)"] Parameters [] Preparation ["No fasting required"] Indications ["Suspected DYT4 dystonia", "Positive family history of dystonia", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 90553-4 ICD-10: G24.1 Clinical summary This genetic test evaluates the TUBB4A gene for mutations associated with DYT4 dystonia.
TEST-2776 Tuberous Sclerosis Complex (TSC) Genetic Testing Test This test detects pathogenic variants in the TSC1 and TSC2 genes associated with Tuberous Sclerosis Complex.	Peripheral whole blood	30 working days	3,100.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in TSC1 gene", "Pathogenic variants in TSC2 gene", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variations (CNVs)"] Parameters [] Preparation ["No fasting required", "Complete the Clinical Exome Testing Requisition Form (Form 36)"] Indications ["Clinical suspicion of TSC based on diagnostic criteria", "Prenatal counseling for families with TSC history", "Determining eligibility for mTOR inhibitor therapy", "Recurrence risk assessment for family members"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q85.1 Clinical summary This test detects pathogenic variants in the TSC1 and TSC2 genes associated with Tuberous Sclerosis Complex.
TEST-2580 TUBGCP6 Gene Microcephaly, Chorioretinopathy & Intellectual Disability Genetic Test This genetic test evaluates the TUBGCP6 gene for variants associated with microcephaly, chorioretinopathy, and intellectual disability.	Whole Blood (EDTA), Extracted DNA, 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 TUBGCP6 gene", "Deletions/Duplications in the TUBGCP6 gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Suspected TUBGCP6-related disorder", "Family history of TUBGCP6-related disorder", "Genetic counselling for affected families"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q02, H31.1, F79 Clinical summary This genetic test evaluates the TUBGCP6 gene for variants associated with microcephaly, chorioretinopathy, and intellectual disability.

Category overview

Genetic: overview

Unlocking the blueprint of your DNA provides profound, proactive insights into your family’s future and personal health risks. Integrated within our advanced Biochemistry and molecular services, specialized Genetic testing evaluates inherited traits, metabolic predispositions, and carrier statuses. Utilizing cutting-edge diagnostic technology, comprehensive genetic screening offers the vital clarity needed to safely guide tailored medical strategies and family planning. As an undisputed leader in innovation among diagnostic labs in Dubai and the UAE, DNA Labs guarantees the highest standards of strict patient confidentiality, unparalleled diagnostic precision, and rapid reporting. Empower your health decisions with certainty—book your genetic testing in UAE, coordinate a secure sample collection, or connect with our specialized genetics team today.

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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.