Diagnostic options · UAE

Genetics tests in Dubai & UAE

Compare available Genetics 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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2,789

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-1.00–50,000.00 AED

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Genetics test prices

Showing 2626–2640 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3286 TSR2 Gene Diamond-Blackfan Anemia Type 14 with Mandibulofacial Dysostosis Genetic Test This test analyzes the TSR2 gene for variants causing Diamond-Blackfan anemia type 14 with mandibulofacial dysostosis.	Whole Blood (EDTA), Extracted DNA, or FTA Card 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 TSR2 gene", "Single nucleotide variants", "Small insertions/deletions", "Copy number variants"] Parameters [] Preparation ["No specific patient preparation required"] Indications ["Suspected Diamond-Blackfan anemia type 14", "Suspected mandibulofacial dysostosis", "Family history of related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 94857-8 ICD-10: D61.0, Q87.0 Clinical summary This test analyzes the TSR2 gene for variants causing Diamond-Blackfan anemia type 14 with mandibulofacial dysostosis.
TEST-5745 TTBK2 Gene Spinocerebellar Ataxia Type 11, Autosomal Dominant Genetic Test This genetic test identifies pathogenic variants in the TTBK2 gene associated with autosomal dominant spinocerebellar ataxia type 11 (SCA11). It uses next-generation sequencing (NG...	Whole blood, 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 TTBK2 gene", "Copy number variants (CNVs) in the TTBK2 gene"] Parameters [] Preparation [] Indications ["Suspected diagnosis of Spinocerebellar Ataxia Type 11 (SCA11)", "Family history of SCA11", "Differential diagnosis of cerebellar ataxia"] Measurement technique Confirm with laboratory Codes LOINC: 95134-8 ICD-10: G11.2 Clinical summary This genetic test identifies pathogenic variants in the TTBK2 gene associated with autosomal dominant spinocerebellar ataxia type 11 (SCA11). It uses next-generation sequencing (NGS) for comprehensive analysis.
TEST-5165 TTC19 Gene Mitochondrial Complex III Deficiency, Nuclear Type 2 Genetic Test This genetic test identifies pathogenic mutations within the TTC19 gene, which are responsible for causing mitochondrial complex III deficiency, a condition affecting neurological...	Whole Blood (2–3 mL EDTA), Extracted DNA (1 µg), 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 mutations in the TTC19 gene", "Mitochondrial complex III deficiency"] Parameters [] Preparation ["Provide detailed clinical history", "Mandatory genetic counselling session", "Avoid CoQ10 or idebenone for 48 hours prior"] Indications ["Confirmation of suspected mitochondrial complex III deficiency", "Carrier screening in families with affected members", "Genetic counseling for reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 83573-1 ICD-10: E88.49 Clinical summary This genetic test identifies pathogenic mutations within the TTC19 gene, which are responsible for causing mitochondrial complex III deficiency, a condition affecting neurological function.
TEST-3663 TTC21B Gene Nephronophthisis type 12 Genetic Test This genetic test analyzes the TTC21B gene to identify mutations associated with Nephronophthisis type 12, a condition affecting multiple organ systems.	Whole Blood (EDTA) or Saliva	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in TTC21B gene", "Single nucleotide variants", "Small insertions/deletions", "Splice-site alterations"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication"] Indications ["Suspected Nephronophthisis type 12", "Family history of NPHP12", "Evaluation of renal cysts", "Investigation of hepatic fibrosis", "Assessment of retinal degeneration"] Measurement technique Confirm with laboratory Codes LOINC: 82319-3 ICD-10: Q61.8, Q61.9 Clinical summary This genetic test analyzes the TTC21B gene to identify mutations associated with Nephronophthisis type 12, a condition affecting multiple organ systems.
TEST-2305 TTC21B Genetic Test (Short-Rib Thoracic Dysplasia Type 4) This test identifies pathogenic mutations in the TTC21B gene associated with short-rib thoracic dysplasia type 4.	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 ["TTC21B gene mutations", "Copy Number Variations (CNVs) in TTC21B"] Parameters [] Preparation ["Fasting is not required", "Stay hydrated", "Inform phlebotomist of bleeding disorders or medications"] Indications ["Suspected diagnosis of Short-Rib Thoracic Dysplasia Type 4", "Family history of TTC21B-related disorders", "Genetic counseling for recurrence risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: Q77.2 Clinical summary This test identifies pathogenic mutations in the TTC21B gene associated with short-rib thoracic dysplasia type 4.
TEST-2704 TTC7A Gene Sequencing Test This test evaluates the TTC7A gene for pathogenic variants linked to multiple intestinal atresia and combined immunodeficiency.	Whole blood, DNA, or dry 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 TTC7A gene", "Copy Number Variations (CNV) within the TTC7A gene"] Parameters [] Preparation ["No special preparation required", "Prior genetic counseling recommended"] Indications ["Diagnosis of multiple intestinal atresia", "Evaluation of combined immunodeficiency", "Genetic counseling for families with affected individuals", "Prenatal diagnosis (with prior counseling and variant confirmation)"] Measurement technique Confirm with laboratory Codes LOINC: 81255-6 ICD-10: Q41.8 Clinical summary This test evaluates the TTC7A gene for pathogenic variants linked to multiple intestinal atresia and combined immunodeficiency.
TEST-3940 TTC8 Gene Bardet-Biedl Syndrome Type 8 Genetic Test This genetic test analyzes the TTC8 gene for mutations associated with Bardet-Biedl Syndrome type 8.	Whole Blood, Extracted DNA, 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 TTC8 gene"] Parameters [] Preparation [] Indications ["Confirmation of suspected Bardet-Biedl Syndrome type 8", "Genetic counseling for individuals with relevant symptoms"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q87.89 Clinical summary This genetic test analyzes the TTC8 gene for mutations associated with Bardet-Biedl Syndrome type 8.
TEST-4332 TTN Gene Cardiomyopathy, Dilated Type 1G (Genetic Test) This genetic test detects pathogenic variants in the TTN gene, a common cause of dilated cardiomyopathy.	Peripheral Whole 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 TTN gene", "Truncating mutations", "Missense variants"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Diagnosis of dilated cardiomyopathy", "Family screening for TTN-related cardiomyopathy", "Genetic counseling for affected families"] Measurement technique Confirm with laboratory Codes LOINC: 82887-6 ICD-10: I42.0 Clinical summary This genetic test detects pathogenic variants in the TTN gene, a common cause of dilated cardiomyopathy.
TEST-4274 TTN Gene Cardiomyopathy, Familial Hypertrophic Type 9 Genetic Test This genetic test identifies pathogenic variants in the TTN gene associated with familial hypertrophic cardiomyopathy type 9.	Peripheral Whole 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 TTN gene", "Copy Number Variations (CNVs) in the TTN gene"] Parameters [] Preparation ["Complete a genetic counseling session", "Provide a detailed clinical history", "Avoid heparin-based blood thinners for 24 hours before collection"] Indications ["Diagnosis of familial hypertrophic cardiomyopathy type 9", "Risk assessment for family members of affected individuals", "Guidance for clinical management and preventive interventions"] Measurement technique Confirm with laboratory Codes LOINC: 92814-2 ICD-10: I42.2 Clinical summary This genetic test identifies pathogenic variants in the TTN gene associated with familial hypertrophic cardiomyopathy type 9.
TEST-4566 TTN Gene Hereditary Myopathy with Early Respiratory Failure Genetic Test This genetic test evaluates the TTN gene for pathogenic variants associated with hereditary myopathy with early respiratory failure (HMERF).	Peripheral whole blood (EDTA, 3–5 mL); alternative: extracted DNA (≥1 µg) or dried blood spot on FTA card. FFPE tissue blocks accepted on a case-by-case basis.	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", "Exon-level Copy Number Variations (CNV)"] Parameters [] Preparation ["Pre-test genetic counselling is mandatory", "No specific fasting or medication adjustments required unless advised by physician"] Indications ["Diagnosis of HMERF", "Genetic counselling for families with HMERF", "Carrier screening in individuals with family history"] Measurement technique Confirm with laboratory Codes LOINC: 21678-5 ICD-10: G71.0 Clinical summary This genetic test evaluates the TTN gene for pathogenic variants associated with hereditary myopathy with early respiratory failure (HMERF).
TEST-5347 TTN Gene Myopathy, Early-Onset with Fatal Cardiomyopathy Genetic Test This genetic test evaluates the entire TTN gene for pathogenic variants associated with early-onset myopathy and fatal cardiomyopathy.	Whole blood (peripheral 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 TTN gene", "Single-nucleotide variants", "Insertions/deletions", "Copy-number changes"] Parameters [] Preparation [] Indications ["Suspected diagnosis of TTN-related early-onset myopathy with fatal cardiomyopathy", "Family history of TTN-related disorders", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 95403-5 ICD-10: G71.2 Clinical summary This genetic test evaluates the entire TTN gene for pathogenic variants associated with early-onset myopathy and fatal cardiomyopathy.
TEST-5827 TTN Gene Sequencing for Tibial Muscular Dystrophy (Tardive) Test This test identifies pathogenic variants in the TTN gene associated with Tibial Muscular Dystrophy (Tardive).	Whole Blood (EDTA), 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 TTN gene", "Single-nucleotide variants", "Small insertions/deletions", "Splice-site mutations"] Parameters [] Preparation ["Pre-test genetic counselling session with pedigree documentation is mandatory.", "Guardian consent required for minors (< 18 years)."] Indications ["Diagnostic confirmation of Tibial Muscular Dystrophy (Tardive)", "Family risk assessment", "Cascade screening of at-risk relatives"] Measurement technique Confirm with laboratory Codes LOINC: 82151-2 ICD-10: G71.0 Clinical summary This test identifies pathogenic variants in the TTN gene associated with Tibial Muscular Dystrophy (Tardive).
TEST-3783 TTR Gene Amyloidosis Genetic Test This test identifies pathogenic variants in the TTR gene associated with hereditary transthyretin amyloidosis.	Whole Blood (EDTA)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TTR gene variants", "Pathogenic mutations"] Parameters [] Preparation ["No fasting required", "Avoid strenuous exercise 2 hours before collection", "Prior genetic counselling is mandatory"] Indications ["Suspected hereditary ATTR amyloidosis", "Family history of ATTR amyloidosis", "Screening of at-risk relatives"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: E85.2 Clinical summary This test identifies pathogenic variants in the TTR gene associated with hereditary transthyretin amyloidosis.
TEST-2634 TUBA1A Gene Lissencephaly Type 3 Genetic Test This test evaluates the TUBA1A gene for pathogenic variants associated with lissencephaly type 3.	Whole Blood (EDTA), Extracted DNA, 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 ["Pathogenic variants in the TUBA1A gene", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["Ensure child is well-hydrated", "No fasting required", "Topical anaesthetic cream may be applied 30 minutes before collection"] Indications ["Suspected diagnosis of lissencephaly type 3", "Family history of lissencephaly", "Genetic counselling for families with affected individuals"] Measurement technique Confirm with laboratory Codes LOINC: 101673-8 ICD-10: Q04.3, Q02, Z13.71 Clinical summary This test evaluates the TUBA1A gene for pathogenic variants associated with lissencephaly type 3.
TEST-5334 TUBB Gene Neurodevelopmental Disorder NGS Test This test evaluates the TUBB gene for variants associated with neurodevelopmental disorders and brain malformations.	Whole Blood (peripheral)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variations (CNVs) in the TUBB gene"] Parameters [] Preparation ["Pre-test genetic counseling is mandatory", "Informed consent required"] Indications ["Individuals with unexplained intellectual disability", "Individuals with cortical dysplasia", "Individuals with epilepsy", "Individuals with lissencephaly spectrum"] Measurement technique Confirm with laboratory Codes LOINC: 92738-5 ICD-10: Q04.8, F70, G40.909 Clinical summary This test evaluates the TUBB gene for variants associated with neurodevelopmental disorders and brain malformations.

Category overview

Genetics: overview

Understanding your unique biological blueprint offers a profound sense of clarity and empowers proactive health planning for you and your family. At DNA Labs UAE, our specialized Genetics division employs state-of-the-art molecular technologies to provide deep insights into hereditary markers and cellular mutations. This comprehensive genetics testing in the UAE equips your healthcare provider with the precise data needed to tailor your medical guidance effectively. Recognized among top diagnostic labs in Dubai and the UAE, we prioritize your peace of mind through strict confidentiality protocols and exceptionally fast, accurate reporting. Take the next step in your health journey. View our genetics diagnostic services, book a private home collection, or consult our specialized team today.

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Genetics tests in Dubai & UAE

Genetics test prices

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