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 721–735 of 805 matching tests.

Genetic diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-2210 TBX3 Gene Ulnar-Mammary Syndrome Genetic Test This test evaluates the entire coding region of the TBX3 gene for pathogenic variants associated with Ulnar-Mammary Syndrome (ULMM). It assesses hereditary cancer predisposition re...	Peripheral Whole Blood (EDTA tube) or FTA Card Finger-Prick	3–4 Weeks (21–28 calendar days); urgent expedite available upon request	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TBX3 gene coding region variants", "Large deletions/duplications in TBX3 gene"] Parameters [] Preparation ["No specific fasting required", "No medication adjustments needed unless advised by physician"] Indications ["Diagnosis of Ulnar-Mammary Syndrome (ULMM)", "Assessment of hereditary cancer predisposition", "Predictive testing for at-risk family members"] Measurement technique Confirm with laboratory Codes LOINC: 78941-3 ICD-10: Q87.2 Clinical summary This test evaluates the entire coding region of the TBX3 gene for pathogenic variants associated with Ulnar-Mammary Syndrome (ULMM). It assesses hereditary cancer predisposition related to TBX3 mutations.
TEST-3118 TBXAS1 Gene Thromboxane Synthase Deficiency Genetic Test This test identifies pathogenic variants in the TBXAS1 gene associated with thromboxane synthase deficiency, a rare inherited platelet disorder.	Whole Blood (EDTA) or Dried Blood Spot (FTA Card)	21–28 Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TBXAS1 gene", "Platelet aggregation function (indirectly via genetic cause)"] Parameters [{"name": "Analytical Sensitivity", "reference_range": ">99.9%"}, {"name": "Analytical Specificity", "reference_range": ">99.9%"}] Preparation ["No special preparation such as fasting is needed", "Avoid strenuous exercise for 24 hours before collection"] Indications ["Suspected thromboxane synthase deficiency", "Evaluation of inherited platelet disorders", "Recurrent unexplained bleeding"] Measurement technique Confirm with laboratory Codes LOINC: 94465-9 ICD-10: D69.1 Clinical summary This test identifies pathogenic variants in the TBXAS1 gene associated with thromboxane synthase deficiency, a rare inherited platelet disorder.
TEST-4580 TCTN3 Gene Joubert Syndrome Type 18 Genetic Test This genetic test identifies pathogenic variants within the TCTN3 gene associated with Joubert syndrome type 18.	Whole Blood (Peripheral)	21–28 Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TCTN3 gene", "Single-nucleotide variants (SNVs)", "Small insertions and deletions (indels)"] Parameters [{"name": "Molecular Coverage", "reference_range": "Full gene coverage (exons, splice sites, deep intronic regions) with uniform read depth"}, {"name": "Analytical Sensitivity", "reference_range": ">99.9% for single-nucleotide variants and small indels"}, {"name": "Diagnostic Yield", "reference_range": ">99.9% for SNVs/indels"}] Preparation [] Indications ["Individuals presenting with clinical features suggestive of Joubert syndrome type 18", "Carrier testing", "Prenatal confirmation", "Variant of uncertain significance resolution"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q04.3 Clinical summary This genetic test identifies pathogenic variants within the TCTN3 gene associated with Joubert syndrome type 18.
TEST-3547 TDRD7 Gene Cataract, Autosomal Recessive Congenital Type 4 Genetic Test This test identifies pathogenic variants in the TDRD7 gene associated with autosomal recessive congenital cataract type 4 (ARCC4).	Peripheral Whole Blood, Dried Blood Spot (FTA card), or Extracted DNA	3–4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TDRD7 gene", "Single nucleotide variants", "Small insertions/deletions", "Copy-number changes (exon level)"] Parameters [] Preparation ["No fasting required", "Genetic counselling session mandatory for informed consent and pedigree chart"] Indications ["Diagnosis of autosomal recessive congenital cataract type 4 (ARCC4)", "Carrier screening", "Family planning", "Guiding early surgical intervention"] Measurement technique Confirm with laboratory Codes LOINC: 81258-2 ICD-10: Q12.0 Clinical summary This test identifies pathogenic variants in the TDRD7 gene associated with autosomal recessive congenital cataract type 4 (ARCC4).
TEST-1084 TEL/AML1 Qualitative Test This test detects the presence of the ETV6-RUNX1 fusion transcript, a common genetic marker in B-cell acute lymphoblastic leukemia (ALL).	Bone Marrow Aspirate or Peripheral Blood	3–4 days	600.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ETV6-RUNX1 fusion transcript", "Presence of specific genetic fusion"] Parameters [] Preparation ["No fasting required", "Inform healthcare team about all current medications", "Valid DHA-licensed physician prescription is mandatory"] Indications ["Diagnosis of B-cell acute lymphoblastic leukemia (ALL)", "Risk stratification in ALL", "Minimal residual disease (MRD) monitoring in ALL"] Measurement technique Confirm with laboratory Codes LOINC: 49797-6 ICD-10: C91.0 Clinical summary This test detects the presence of the ETV6-RUNX1 fusion transcript, a common genetic marker in B-cell acute lymphoblastic leukemia (ALL).
TEST-3552 TENM1 Gene Colobomatous Microphthalmia Genetic Test This diagnostic test evaluates the TENM1 gene for pathogenic variants associated with colobomatous microphthalmia.	Whole Blood, Dried Blood Spot (FTA Card), 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 TENM1 gene", "Single nucleotide variants", "Small insertions and deletions", "Copy number changes"] Parameters [] Preparation ["No fasting required", "Pre-test genetic counselling session mandatory", "Provide previous ophthalmology reports", "Legal guardian accompaniment required for minors"] Indications ["Clinical suspicion of colobomatous microphthalmia", "Family history of colobomatous microphthalmia", "Need for recurrence risk counselling"] Measurement technique Confirm with laboratory Codes LOINC: 48018-6 ICD-10: Q11.2, Q12.2 Clinical summary This diagnostic test evaluates the TENM1 gene for pathogenic variants associated with colobomatous microphthalmia.
TEST-2981 TFAP2B Gene Char Syndrome Genetic Test This genetic test evaluates the TFAP2B gene for mutations associated with Char syndrome.	Peripheral whole blood (or FTA card for neonates)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TFAP2B gene sequence", "Single nucleotide variants (SNVs)", "Insertions/Deletions (indels)", "Mosaic mutations"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any recent blood transfusions or transplants"] Indications ["Suspected Char syndrome", "Family history of Char syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 81319-5 ICD-10: Q87.8 Clinical summary This genetic test evaluates the TFAP2B gene for mutations associated with Char syndrome.
TEST-3467 TG Gene Thyroid Dyshormonogenesis Type 3 Genetic Test This genetic test detects pathogenic variants in the thyroglobulin (TG) gene associated with congenital hypothyroidism and goitre.	Whole Blood (Peripheral)	21 calendar days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TG gene", "Full coding region and splice sites of the TG gene"] Parameters [] Preparation ["No specific patient preparation required"] Indications ["Suspected thyroid dyshormonogenesis", "Congenital hypothyroidism with goitre", "Family history of thyroid disorders"] Measurement technique Confirm with laboratory Codes LOINC: 98137-4 ICD-10: E07.1, Z13.29, Z14.8 Clinical summary This genetic test detects pathogenic variants in the thyroglobulin (TG) gene associated with congenital hypothyroidism and goitre.
TEST-3026 TGFB1 Gene Camurati‑Engelmann Disease Genetic Test This test evaluates the entire coding region and splice sites of the TGFB1 gene for variants associated with Camurati-Engelmann disease.	Whole blood (EDTA), extracted genomic DNA, or FTA card spot	3 to 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TGFB1 gene variants", "Single nucleotide variants (SNVs)", "Insertions/Deletions (Indels)"] Parameters [] Preparation ["Pre-test genetic counselling required", "Written informed consent required", "Three-generation pedigree chart required"] Indications ["Suspected Camurati-Engelmann disease", "Progressive diaphyseal dysplasia", "Family history of bone dysplasias"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: Q78.3 Clinical summary This test evaluates the entire coding region and splice sites of the TGFB1 gene for variants associated with Camurati-Engelmann disease.
TEST-4823 TGFBR1 Gene Loeys-Dietz Syndrome Type 1A Genetic Test This test detects pathogenic variants in the TGFBR1 gene associated with Loeys-Dietz syndrome type 1A.	EDTA whole blood, 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 TGFBR1 gene", "Copy Number Variants (CNVs) in TGFBR1"] Parameters [] Preparation ["No specific fasting required", "Continue prescribed medications unless advised otherwise by a physician"] Indications ["Suspected diagnosis of Loeys-Dietz syndrome type 1A", "Family history of Loeys-Dietz syndrome", "Genetic counseling for at-risk individuals"] Measurement technique Confirm with laboratory Codes LOINC: 81307-4 ICD-10: Q87.89 Clinical summary This test detects pathogenic variants in the TGFBR1 gene associated with Loeys-Dietz syndrome type 1A.
TEST-2751 TGIF1 Gene Holoprosencephaly Type 4 Genetic Test This genetic test analyzes the TGIF1 gene to detect pathogenic variants associated with holoprosencephaly type 4.	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 TGIF1 gene", "Coding regions and splice sites of the TGIF1 gene"] Parameters [] Preparation ["No special preparation is needed", "Do not discontinue prescribed medications"] Indications ["Suspected holoprosencephaly type 4", "Family history of holoprosencephaly", "Need for precise prognosis and recurrence risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: Q04.2 Clinical summary This genetic test analyzes the TGIF1 gene to detect pathogenic variants associated with holoprosencephaly type 4.
TEST-5677 TH Gene Segawa Syndrome, Autosomal Recessive Genetic Test This test evaluates the tyrosine hydroxylase (TH) gene for pathogenic variants associated with autosomal recessive Segawa syndrome (dopa-responsive dystonia). It utilizes Next-Gene...	Whole blood (EDTA), pre-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 TH gene", "Single nucleotide variants (SNVs)", "Insertions/deletions (indels)", "Copy number variations (CNVs)"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any current medications"] Indications ["Suspected Segawa syndrome (dopa-responsive dystonia)", "Early-onset dystonia of unknown cause", "Family history of Segawa syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 81309-1 ICD-10: G24.1 Clinical summary This test evaluates the tyrosine hydroxylase (TH) gene for pathogenic variants associated with autosomal recessive Segawa syndrome (dopa-responsive dystonia). It utilizes Next-Generation Sequencing (NGS) for comprehensive analysis.
TEST-3265 Thalassemia Beta Complete Gene Analysis with Maternal Cell Contamination (MCC) Test This test evaluates the fetal beta-globin gene for mutations associated with beta-thalassemia and confirms the absence of maternal cell contamination.	Amniotic fluid or Chorionic Villus Sample	21 Working Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Fetal beta-globin gene pathogenic variants", "Maternal Cell Contamination (MCC)"] Parameters [] Preparation ["Discuss complete medical history with the referring specialist.", "Do not discontinue prescribed medication without explicit instruction from the supervising physician."] Indications ["Prenatal screening for beta-thalassemia", "Risk assessment based on parental carrier status", "Ultrasound findings suggestive of fetal anemia"] Measurement technique Confirm with laboratory Codes LOINC: 21620-0 ICD-10: D56.1 Clinical summary This test evaluates the fetal beta-globin gene for mutations associated with beta-thalassemia and confirms the absence of maternal cell contamination.
TEST-3259 Thalassemia Beta Mutation Analysis Test This test identifies pathogenic variants in the HBB gene associated with beta-thalassemia.	Peripheral Whole Blood (Lavender Top EDTA)	5 working days	1,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the HBB gene"] Parameters [] Preparation [] Indications ["Diagnostic confirmation of beta-thalassemia", "Carrier screening", "Informed reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 46738-3 ICD-10: D56.1, D56.9, Z31.430 Clinical summary This test identifies pathogenic variants in the HBB gene associated with beta-thalassemia.
TEST-4532 THSD1 Gene Thrombospondin Type 1 Domain-Containing Protein 1 Genetic Test This test evaluates the entire coding region and splice sites of the THSD1 gene for pathogenic variants.	Peripheral Blood, FTA Card, or Extracted DNA	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 THSD1 gene coding regions", "Pathogenic variants in THSD1 gene splice sites"] Parameters [] Preparation ["No fasting required", "No specific medication or diet restrictions"] Indications ["Suspected hereditary disorders affecting bone", "Suspected hereditary disorders affecting skin", "Suspected hereditary disorders affecting the immune system"] Measurement technique Confirm with laboratory Codes LOINC: 88850-6 ICD-10: Z13.71 Clinical summary This test evaluates the entire coding region and splice sites of the THSD1 gene for pathogenic variants.

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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