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 31–45 of 805 matching tests.

Genetic diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3151 ADAMTS13 Gene Thrombotic Thrombocytopenic Purpura (TTP) Genetic Test This genetic test identifies mutations in the ADAMTS13 gene associated with congenital Thrombotic Thrombocytopenic Purpura (TTP).	Whole Blood (EDTA) or FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ADAMTS13 gene mutations", "Carrier status for congenital TTP"] Parameters [] Preparation ["No fasting required", "Continue regular medications unless instructed otherwise"] Indications ["Diagnosis of congenital TTP", "Carrier screening", "Family planning"] Measurement technique Confirm with laboratory Codes LOINC: 81311-5 ICD-10: M31.1 Clinical summary This genetic test identifies mutations in the ADAMTS13 gene associated with congenital Thrombotic Thrombocytopenic Purpura (TTP).
TEST-5193 ADAMTS2 Gene Ehlers-Danlos Syndrome Type 7C (Dermatosparaxis) Genetic Test This genetic test analyzes the ADAMTS2 gene for mutations associated with Ehlers-Danlos syndrome type VIIC (dermatosparaxis). It identifies pathogenic variants to confirm diagnosis...	Peripheral whole blood	3–4 Weeks (Rush option available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ADAMTS2 gene sequence", "Pathogenic variants (mutations)", "Copy Number Variations (CNV)"] Parameters [] Preparation ["No specific fasting required.", "Inform the lab about recent blood transfusions ( Indications ["Clinical suspicion of Ehlers-Danlos syndrome type VIIC (dermatosparaxis)", "Family history of dermatosparaxis", "Need for definitive genetic diagnosis for management and counseling"] Measurement technique Confirm with laboratory Codes LOINC: 81247-7 ICD-10: Q79.6, Z14.01, Z82.79 Clinical summary This genetic test analyzes the ADAMTS2 gene for mutations associated with Ehlers-Danlos syndrome type VIIC (dermatosparaxis). It identifies pathogenic variants to confirm diagnosis and guide patient management.
TEST-3609 ADAMTSL4 Gene Ectopia Lentis et Pupillae Genetic Test This test detects pathogenic variants in the ADAMTSL4 gene associated with ectopia lentis et pupillae.	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 ["Pathogenic variants in the ADAMTSL4 gene", "Full gene sequencing (exons, flanking introns, deep intronic variants)"] Parameters [] Preparation ["No fasting required", "Provide completed clinical history form", "Provide pedigree chart"] Indications ["Diagnosis of ectopia lentis et pupillae", "Differentiation from Marfan syndrome and homocystinuria", "Carrier screening", "Familial risk assessment", "Pre-surgical planning"] Measurement technique Confirm with laboratory Codes LOINC: 51234-5 ICD-10: Q12.1, H27.1 Clinical summary This test detects pathogenic variants in the ADAMTSL4 gene associated with ectopia lentis et pupillae.
TEST-3605 ADAR Gene Dyschromatosis Symmetrica Hereditaria Genetic Test This test identifies pathogenic variants in the ADAR gene associated with Dyschromatosis Symmetrica Hereditaria (DSH).	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 ADAR gene", "Full coding region and splice sites"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications without consulting your physician"] Indications ["Confirmation of clinical diagnosis of DSH", "Family screening for DSH", "Genetic counselling"] Measurement technique Confirm with laboratory Codes LOINC: 43401-2 ICD-10: Q82.8, Z13.79, Z14.8 Clinical summary This test identifies pathogenic variants in the ADAR gene associated with Dyschromatosis Symmetrica Hereditaria (DSH).
TEST-4174 ADCY5 Gene Dyskinesia, Familial, with Facial Myokymia Genetic Test This genetic test identifies pathogenic variants in the ADCY5 gene associated with familial dyskinesia with facial myokymia.	Peripheral whole blood (EDTA tube) 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 the ADCY5 gene"] Parameters [] Preparation ["Provide detailed clinical history", "Attend mandatory genetic counselling session"] Indications ["Suspected familial dyskinesia with facial myokymia", "Differential diagnosis of movement disorders"] Measurement technique Confirm with laboratory Codes LOINC: 83429-6 ICD-10: G25.89 Clinical summary This genetic test identifies pathogenic variants in the ADCY5 gene associated with familial dyskinesia with facial myokymia.
TEST-2732 ADK Gene Hypermethioninemia due to Adenosine Kinase Deficiency Genetic Test This genetic test evaluates the adenosine kinase (ADK) gene for pathogenic variants associated with hypermethioninemia.	Peripheral whole blood	3-4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Adenosine Kinase (ADK) gene sequence", "Pathogenic variants (SNVs, indels)"] Parameters [] Preparation ["No special preparation needed beyond routine hydration", "Complimentary genetic counselling session provided"] Indications ["Suspected Adenosine Kinase Deficiency", "Hypermethioninemia", "Family history of the disorder", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 101404-3 ICD-10: E72.11 Clinical summary This genetic test evaluates the adenosine kinase (ADK) gene for pathogenic variants associated with hypermethioninemia.
TEST-6123 AGA Gene Aspartylglucosaminuria Genetic Test This test performs full-coding-region sequencing of the AGA gene to detect pathogenic point mutations, small insertions or deletions, and copy-number variants associated with aspar...	Peripheral Whole Blood (EDTA), Extracted DNA, or FTA Blood Spot	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["AGA gene sequence", "Pathogenic variants (point mutations, insertions, deletions, copy-number variants)"] Parameters [] Preparation ["Complete pre-test genetic counseling session", "Provide a three-generation family pedigree"] Indications ["Diagnosis of aspartylglucosaminuria", "Carrier screening", "Prenatal testing"] Measurement technique Confirm with laboratory Codes LOINC: 94227-4 ICD-10: E77.1 Clinical summary This test performs full-coding-region sequencing of the AGA gene to detect pathogenic point mutations, small insertions or deletions, and copy-number variants associated with aspartylglucosaminuria.
TEST-3524 AGK Gene Cataract, Autosomal Recessive Type 38 Genetic Test This genetic test detects mutations in the AGK gene associated with congenital cataract and mitochondrial dysfunction.	Whole Blood (Peripheral)	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Mutations in the AGK gene"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist about anticoagulant therapy"] Indications ["Suspected autosomal recessive cataract type 38", "Family history of AGK-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 91727-1 ICD-10: Q12.0 Clinical summary This genetic test detects mutations in the AGK gene associated with congenital cataract and mitochondrial dysfunction.
TEST-3523 AGTR1 Gene Renal Tubular Dysgenesis Genetic Test This test identifies pathogenic mutations in the AGTR1 gene associated with autosomal recessive renal tubular dysgenesis.	Peripheral Whole Blood (EDTA) 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 AGTR1 gene", "Single nucleotide variants", "Small insertions/deletions", "Splice-site alterations"] Parameters [] Preparation [] Indications ["Diagnosis of suspected autosomal recessive renal tubular dysgenesis", "Family risk assessment", "Informed clinical management", "Carrier screening", "Family planning"] Measurement technique Confirm with laboratory Codes LOINC: 90507-6 ICD-10: Q61.4 Clinical summary This test identifies pathogenic mutations in the AGTR1 gene associated with autosomal recessive renal tubular dysgenesis.
TEST-5050 AGTR2 Gene Intellectual Disability (X-linked, MRX88) Genetic Test This genetic test analyzes the AGTR2 gene to detect mutations causing X-linked intellectual disability (MRX88). It identifies single-nucleotide variants, small insertions/deletions...	Peripheral Whole Blood – EDTA (2 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 AGTR2 gene", "Single-nucleotide variants", "Small insertions/deletions", "Splice-site mutations"] Parameters [] Preparation ["Genetic counseling session is mandatory before sample collection."] Indications ["Individuals with unexplained developmental delay", "Suspected X-linked intellectual disability (MRX88)", "Family history suggestive of X-linked inheritance"] Measurement technique Confirm with laboratory Codes LOINC: 82203-0 ICD-10: F78 Clinical summary This genetic test analyzes the AGTR2 gene to detect mutations causing X-linked intellectual disability (MRX88). It identifies single-nucleotide variants, small insertions/deletions, and splice-site mutations.
TEST-4674 AHI1 Gene (Joubert Syndrome Type 3) Genetic Test This genetic test evaluates the AHI1 gene for variants associated with Joubert syndrome type 3.	Whole Blood (EDTA)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["AHI1 gene sequence", "Copy Number Variations (CNVs) in AHI1"] Parameters [] Preparation ["No fasting required", "Provide detailed clinical history", "Attend mandatory pre-genetic counselling session", "Bring previous MRI reports, neurology notes, and a list of current medications"] Indications ["Suspected Joubert syndrome type 3", "Family history of Joubert syndrome type 3", "Developmental delay with characteristic neuroimaging findings"] Measurement technique Confirm with laboratory Codes LOINC: 94425-5 ICD-10: Q04.3 Clinical summary This genetic test evaluates the AHI1 gene for variants associated with Joubert syndrome type 3.
TEST-5186 AKAP1 Gene Mitochondrial Disorders Genetic Test This test identifies pathogenic variants in the AKAP1 gene associated with mitochondrial encephalopathies.	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 AKAP1 gene", "Single-nucleotide variants", "Small insertions and deletions"] Parameters [] Preparation ["Inform the geneticist about all current medications and supplements.", "Do not discontinue any prescribed therapy without consulting your physician."] Indications ["Suspected mitochondrial encephalopathy", "Family history of AKAP1-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 82939-8 ICD-10: G71.3, G31.89, Z13.79 Clinical summary This test identifies pathogenic variants in the AKAP1 gene associated with mitochondrial encephalopathies.
TEST-6029 AKR1D1 Gene Bile Acid Synthesis Defect Type 2 Congenital Genetic Test This genetic test identifies disease-causing variants in the AKR1D1 gene, confirming a diagnosis of congenital bile acid synthesis defect 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 the AKR1D1 gene", "Presence/absence of mutations affecting bile acid synthesis"] Parameters [] Preparation ["No fasting required", "Genetic counseling and informed consent required prior to collection"] Indications ["Infants with suspected bile acid synthesis defect type 2", "Neonatal cholestasis of unknown origin", "Family history of AKR1D1-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 79765-3 ICD-10: E78.7, Z15.89, K76.8 Clinical summary This genetic test identifies disease-causing variants in the AKR1D1 gene, confirming a diagnosis of congenital bile acid synthesis defect type 2.
TEST-5950 ALDH2 Gene Acute Alcohol Sensitivity Genetic Test This genetic test evaluates functional variants within the ALDH2 gene to determine an individual's capacity to metabolize acetaldehyde, the toxic intermediate of alcohol.	Peripheral Whole Blood	21–28 Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Functional variants in the ALDH2 gene", "Acetaldehyde metabolism capacity"] Parameters [] Preparation [] Indications ["Assessment of acute alcohol sensitivity", "Risk assessment for alcohol-related health issues", "Personalized advice on alcohol intake"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Z13.89 Clinical summary This genetic test evaluates functional variants within the ALDH2 gene to determine an individual's capacity to metabolize acetaldehyde, the toxic intermediate of alcohol.
TEST-6198 ALDH4A1 Gene Hyperprolinemia Type 2 Genetic Test This genetic test identifies pathogenic variants in the ALDH4A1 gene associated with Hyperprolinemia type 2.	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 ["Pathogenic variants in the ALDH4A1 gene"] Parameters [] Preparation ["No fasting required", "Pre-test genetic counselling session mandatory"] Indications ["Suspected Hyperprolinemia type 2", "Family history of Hyperprolinemia type 2", "Evaluation of inborn errors of metabolism"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: E72.52 Clinical summary This genetic test identifies pathogenic variants in the ALDH4A1 gene associated with Hyperprolinemia type 2.

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.