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 2521–2535 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5775 TECTA Gene Autosomal Dominant Deafness Type 12 Genetic Test This genetic test analyzes the TECTA gene for mutations causing autosomal dominant non-syndromic hearing loss (DFNA12). It provides a definitive molecular diagnosis.	Peripheral Whole Blood (EDTA, 3-5 mL)	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 TECTA gene", "Exon coverage of the TECTA gene"] Parameters [] Preparation ["No fasting required", "No alteration to medication schedule required"] Indications ["Children and adults with early-onset, bilateral sensorineural hearing loss", "Presence of at least one first-degree relative with confirmed hearing impairment"] Measurement technique Confirm with laboratory Codes LOINC: 83397-6 ICD-10: H90.5 Clinical summary This genetic test analyzes the TECTA gene for mutations causing autosomal dominant non-syndromic hearing loss (DFNA12). It provides a definitive molecular diagnosis.
TEST-1081 TEL/AML1 (ALL) Genetics Testing Test This test identifies the ETV6-RUNX1 gene fusion, a common genetic marker associated with a favorable prognosis in pediatric B-cell ALL.	Bone Marrow Aspirate / Peripheral Blood	3–4 working days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ETV6-RUNX1 gene fusion", "t(12;21)(p13;q22) translocation"] Parameters [] Preparation ["No specific patient preparation required."] Indications ["Risk stratification in pediatric B-cell ALL", "Guiding chemotherapy protocol selection", "Prognostic assessment"] Measurement technique Confirm with laboratory Codes LOINC: 33676-7 ICD-10: C91.0 Clinical summary This test identifies the ETV6-RUNX1 gene fusion, a common genetic marker associated with a favorable prognosis in pediatric B-cell ALL.
TEST-5200 TERT Gene Dyskeratosis Congenita Genetic Test This genetic test evaluates the TERT gene for mutations associated with Dyskeratosis Congenita, a disorder affecting telomere maintenance.	Whole Blood (EDTA), 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 ["TERT gene mutations (point mutations, small insertions/deletions, copy number variations)"] Parameters [] Preparation ["Fasting for 8–12 hours is advised only if a concurrent metabolic panel is ordered.", "Provide a complete medication list to the genetic counselor.", "Parental/guardian consent required for minors."] Indications ["Suspected Dyskeratosis Congenita", "Diagnosis of telomere biology disorders", "Guiding cancer surveillance", "Family planning in affected families"] Measurement technique Confirm with laboratory Codes LOINC: 48018-6 ICD-10: Q82.8, D61.09 Clinical summary This genetic test evaluates the TERT gene for mutations associated with Dyskeratosis Congenita, a disorder affecting telomere maintenance.
TEST-4624 TERT Gene Sequencing (NGS) for Pulmonary Fibrosis & Bone Marrow Failure Telomeropathy Test This test analyzes the TERT gene for mutations associated with pulmonary fibrosis and bone marrow failure syndromes.	Peripheral Whole Blood (EDTA tube)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TERT gene pathogenic variants", "Telomere-related disease risk"] Parameters [] Preparation ["Pre-test genetic counseling is mandatory", "No fasting required", "Provide detailed clinical history and family records"] Indications ["Suspected familial pulmonary fibrosis", "Suspected dyskeratosis congenita", "Suspected aplastic anemia due to telomere dysfunction"] Measurement technique Confirm with laboratory Codes LOINC: 82182-7 ICD-10: J84.112, D61.9, Z15.89 Clinical summary This test analyzes the TERT gene for mutations associated with pulmonary fibrosis and bone marrow failure syndromes.
TEST-3035 TFAP2A Gene Branchiooculofacial Syndrome Genetic Test This test identifies mutations in the TFAP2A gene associated with Branchiooculofacial syndrome.	Whole blood (EDTA tube), buccal swab, 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 ["Mutations in the TFAP2A gene", "Point mutations", "Small indels", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["No dietary or medication restrictions", "Provide complete clinical history and previous genetic reports"] Indications ["Suspected Branchiooculofacial syndrome", "Family history of BOFS", "Carrier screening", "Prenatal diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 21624-1 ICD-10: Q87.0 Clinical summary This test identifies mutations in the TFAP2A gene associated with Branchiooculofacial syndrome.
TEST-5686 TFG Gene (SPG57) Genetic Test This test detects pathogenic variants in the TFG gene associated with autosomal recessive hereditary spastic paraplegia type 57 (SPG57).	Peripheral Blood 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 TFG gene"] Parameters [] Preparation ["No fasting required", "No medication changes required"] Indications ["Confirmation of clinical diagnosis of SPG57", "Family planning for individuals with SPG57", "Differential diagnosis of neurological disorders"] Measurement technique Confirm with laboratory Codes LOINC: 91518-1 ICD-10: G11.4 Clinical summary This test detects pathogenic variants in the TFG gene associated with autosomal recessive hereditary spastic paraplegia type 57 (SPG57).
TEST-3990 TGFB2 Gene Loeys-Dietz Syndrome Type 4 Genetic Test This test identifies pathogenic variants in the TGFB2 gene associated with Loeys-Dietz syndrome type 4, an inherited connective tissue disorder.	Whole Blood (EDTA), Extracted DNA, 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 TGFB2 gene", "Single nucleotide variants", "Insertions", "Deletions", "Copy number changes"] Parameters [] Preparation ["No fasting or special preparation required"] Indications ["Personal or family history of aortic root enlargement", "Early-onset arterial aneurysms", "Suspected Loeys-Dietz spectrum disorders"] Measurement technique Confirm with laboratory Codes LOINC: 44127-1 ICD-10: Q87.89 Clinical summary This test identifies pathogenic variants in the TGFB2 gene associated with Loeys-Dietz syndrome type 4, an inherited connective tissue disorder.
TEST-4443 TGFB3 Gene Arrhythmogenic Right Ventricular Cardiomyopathy Type 1 Genetic Test This genetic test analyzes the TGFB3 gene for variants associated with Arrhythmogenic Right Ventricular Cardiomyopathy Type 1 (ARVC1). It identifies mutations linked to an inherite...	Whole Blood, 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 ["Single-nucleotide variants in TGFB3 gene", "Small insertions or deletions in TGFB3 gene", "Exon-level copy number changes in TGFB3 gene"] Parameters [] Preparation [] Indications ["Clinical suspicion of Arrhythmogenic Right Ventricular Cardiomyopathy Type 1 (ARVC1)", "Family history of ARVC1", "Cascade screening of at-risk family members"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: I42.8 Clinical summary This genetic test analyzes the TGFB3 gene for variants associated with Arrhythmogenic Right Ventricular Cardiomyopathy Type 1 (ARVC1). It identifies mutations linked to an inherited heart muscle disorder increasing risk for arrhythmias and sudden cardiac arrest.
TEST-3588 TGFBI Gene Corneal Dystrophy Genetic Testing (NGS) Test This test identifies pathogenic variants in the TGFBI gene associated with epithelial basement membrane corneal dystrophy.	Peripheral whole blood (venous) or FTA card (dried blood spot) or previously extracted DNA	3 to 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 TGFBI gene"] Parameters [] Preparation ["No fasting or dietary restrictions required", "Inform the team of any anticoagulant use", "Mandatory pre-test genetic counselling session required"] Indications ["Diagnosis of epithelial basement membrane corneal dystrophy", "Genetic counselling for families with corneal dystrophy", "Guiding management planning for hereditary corneal conditions"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: H18.53 Clinical summary This test identifies pathogenic variants in the TGFBI gene associated with epithelial basement membrane corneal dystrophy.
TEST-4062 TGFBR1 Gene Aortic Aneurysm, Familial Thoracic Type 5 Genetic Test This test evaluates the TGFBR1 gene for pathogenic variants associated with familial thoracic aortic aneurysm type 5 and Loeys‑Dietz syndrome.	Whole Blood (EDTA)	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TGFBR1 gene variants", "Pathogenic mutations"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Diagnosis of familial thoracic aortic aneurysm type 5", "Diagnosis of Loeys‑Dietz syndrome", "Risk assessment in families with aortic aneurysms", "Genotype-phenotype correlation studies"] Measurement technique Confirm with laboratory Codes LOINC: 88518-6 ICD-10: I71.2, I71.3 Clinical summary This test evaluates the TGFBR1 gene for pathogenic variants associated with familial thoracic aortic aneurysm type 5 and Loeys‑Dietz syndrome.
TEST-4834 TGFBR1 Gene Loeys-Dietz Syndrome Type 2A Genetic Test (NGS) This molecular diagnostic test identifies pathogenic variants in the TGFBR1 gene, which are causative for Loeys-Dietz syndrome type 2A.	Peripheral whole blood (3–5 mL in EDTA tube) 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 coding region"] Parameters [] Preparation ["Prior genetic counselling required", "Detailed three-generation pedigree chart required", "Written informed consent required"] Indications ["Clinical suspicion of Loeys-Dietz syndrome type 2A", "Family history of Loeys-Dietz syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 82994-1 ICD-10: Q87.89, Q87.8 Clinical summary This molecular diagnostic test identifies pathogenic variants in the TGFBR1 gene, which are causative for Loeys-Dietz syndrome type 2A.
TEST-4795 TGFBR1 Gene Sequencing for Marfan Syndrome Test This test sequences the entire TGFBR1 gene to identify pathogenic variants associated with Marfan syndrome and related connective tissue disorders.	Peripheral whole blood (2 mL EDTA) or buccal swab	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TGFBR1 gene sequence", "Pathogenic variants (SNVs, small indels)"] Parameters [] Preparation [] Indications ["Clinical diagnosis or suspicion of Marfan syndrome based on revised Ghent criteria", "First-degree relative with known pathogenic TGFBR1 variant", "Family history of unexplained aortic aneurysm or dissection"] Measurement technique Confirm with laboratory Codes LOINC: 81763-4 ICD-10: Q87.40, Z15.89, Z84.81 Clinical summary This test sequences the entire TGFBR1 gene to identify pathogenic variants associated with Marfan syndrome and related connective tissue disorders.
TEST-4066 TGFBR2 Gene Aortic Aneurysm, Familial Thoracic Type 3 Genetic Test This test identifies genetic variants in the TGFBR2 gene associated with an increased risk of familial thoracic aortic aneurysm type 3.	Peripheral Whole Blood (5–10 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 TGFBR2 gene", "Copy Number Variations (CNV) in the TGFBR2 gene"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any medications"] Indications ["Individuals with a family history of familial thoracic aortic aneurysm type 3", "Individuals with unexplained aortic root dilation or dissection"] Measurement technique Confirm with laboratory Codes LOINC: 81408-6 ICD-10: I71.2 Clinical summary This test identifies genetic variants in the TGFBR2 gene associated with an increased risk of familial thoracic aortic aneurysm type 3.
TEST-2094 TGFBR2 Gene Colorectal Cancer, Hereditary Nonpolyposis Type 6 Genetic Test This test evaluates the entire TGFBR2 gene for germline mutations associated with an increased risk of hereditary colorectal cancer.	Whole blood (Peripheral)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Germline mutations in the TGFBR2 gene", "Pathogenic variants", "Likely pathogenic variants", "Variants of uncertain significance (VUS)"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any anticoagulant therapy"] Indications ["Individuals with a personal or family history suggestive of Lynch syndrome", "Patients meeting specific clinical criteria for hereditary cancer risk assessment", "Pre-test genetic counselling completed"] Measurement technique Confirm with laboratory Codes LOINC: 48000-4 ICD-10: Z15.09 Clinical summary This test evaluates the entire TGFBR2 gene for germline mutations associated with an increased risk of hereditary colorectal cancer.
TEST-4809 TGFBR2 Gene Genetic Test (Loeys‑Dietz Syndrome Type 2 / Marfanoid Syndromes) This test evaluates the TGFBR2 gene for mutations associated with Loeys-Dietz syndrome type 2 and related connective tissue disorders.	Whole blood (3-5 mL), extracted DNA (2 µg), 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 ["TGFBR2 gene sequence", "Copy number variations in TGFBR2", "Pathogenic variants (SNVs, indels, CNVs)"] Parameters [] Preparation ["No fasting required", "No medication changes required", "No special preparation needed"] Indications ["Diagnosis of Loeys-Dietz syndrome type 2", "Diagnosis of related Marfanoid disorders", "Family history of TGFBR2-related conditions", "Unexplained aortic pathology", "Risk assessment for individuals with suspected hereditary connective tissue disease"] Measurement technique Confirm with laboratory Codes LOINC: 76023-6 ICD-10: Q87.4 Clinical summary This test evaluates the TGFBR2 gene for mutations associated with Loeys-Dietz syndrome type 2 and related connective tissue disorders.

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

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