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.

Tests in this category

2,789

Listed price range

-1.00–50,000.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Genetics test prices

Showing 61–75 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5985 ACY1 Gene Aminoacylase Deficiency Genetic Test This genetic test evaluates for pathogenic mutations within the ACY1 gene associated with aminoacylase deficiency.	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 mutations in the ACY1 gene", "Amino acid catabolism impairment"] Parameters [] Preparation ["No fasting needed unless paired with other metabolic labs"] Indications ["Suspected aminoacylase deficiency", "Family history of aminoacylase deficiency", "Evaluation of metabolic disorders"] Measurement technique Confirm with laboratory Codes LOINC: 82301-8 ICD-10: E72.8 Clinical summary This genetic test evaluates for pathogenic mutations within the ACY1 gene associated with aminoacylase deficiency.
TEST-4000 ADA2 Gene (CECR1) Genetic Testing for DADA2 & Sneddon Syndrome Test This test evaluates the entire ADA2 gene for pathogenic variants associated with Deficiency of Adenosine Deaminase 2 (DADA2) and related conditions like Sneddon syndrome.	Whole Blood (Peripheral)	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 ADA2 gene", "Gene coverage of all exons, intron/exon boundaries, and promoter region"] Parameters [] Preparation ["No fasting required", "No special preparation needed", "Mandatory pre-test genetic counseling is required"] Indications ["Suspected DADA2 based on clinical presentation", "Family history of DADA2", "Differential diagnosis of autoinflammatory vasculitis", "Evaluation of Sneddon syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 92879-2 ICD-10: E79.8 Clinical summary This test evaluates the entire ADA2 gene for pathogenic variants associated with Deficiency of Adenosine Deaminase 2 (DADA2) and related conditions like Sneddon syndrome.
TEST-3750 ADAM10 Gene Alzheimer Disease Type 18 Susceptibility Test This test evaluates the ADAM10 gene for mutations associated with an increased risk of early-onset Alzheimer disease type 18.	Peripheral Whole Blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ADAM10 gene sequence", "Single nucleotide variants", "Deletions", "Duplications", "CNV analysis"] Parameters [] Preparation [] Indications ["Individuals with a strong family history of early-onset dementia", "Predictive risk assessment for AD18"] Measurement technique Confirm with laboratory Codes LOINC: 101523-5 ICD-10: G30.0, Z15.89, Z82.0 Clinical summary This test evaluates the ADAM10 gene for mutations associated with an increased risk of early-onset Alzheimer disease type 18.
TEST-4604 ADAM10 Gene Sequencing for Reticulate Acropigmentation of Kitamura (RAK) Test This test identifies pathogenic variants in the ADAM10 gene associated with Reticulate Acropigmentation of Kitamura (RAK).	Peripheral whole blood	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 ADAM10 gene"] Parameters [] Preparation [] Indications ["Clinical features consistent with reticulate acropigmentation of Kitamura", "At-risk family members of a confirmed case"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: L81.8 Clinical summary This test identifies pathogenic variants in the ADAM10 gene associated with Reticulate Acropigmentation of Kitamura (RAK).
TEST-4874 ADAM17 Gene Inflammatory Skin and Bowel Disease, Neonatal, Type 1 Genetic Test This genetic test identifies pathogenic variants in the ADAM17 gene associated with a rare neonatal syndrome.	Peripheral whole blood	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 ADAM17 gene"] Parameters [] Preparation ["No fasting required"] Indications ["Suspected ADAM17-related neonatal inflammatory skin and bowel disease type 1", "Neonatal onset of severe skin lesions and intractable diarrhoea"] Measurement technique Confirm with laboratory Codes LOINC: 93025-5 ICD-10: Q87.89, P83.8, K90.8 Clinical summary This genetic test identifies pathogenic variants in the ADAM17 gene associated with a rare neonatal syndrome.
TEST-3606 ADAM9 Gene Cone‑Rod Dystrophy Type 9 Genetic Test This test identifies pathogenic variants in the ADAM9 gene associated with cone-rod dystrophy type 9.	Whole Blood (Peripheral)	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 ADAM9 gene", "Copy Number Variations (CNV)", "Single Nucleotide Variants (SNV)"] Parameters [] Preparation ["No specific fasting required", "Avoid recent blood transfusion (within 2 weeks)"] Indications ["Suspected diagnosis of cone-rod dystrophy type 9", "Family history of inherited retinal disorders", "Need for genetic confirmation for prognosis and management"] Measurement technique Confirm with laboratory Codes LOINC: 83464-7 ICD-10: H35.5 Clinical summary This test identifies pathogenic variants in the ADAM9 gene associated with cone-rod dystrophy type 9.
TEST-5094 ADAMTSL2 Gene Geleophysic Dysplasia Type 1 Genetic Test This genetic test analyzes the ADAMTSL2 gene to identify pathogenic variants associated with Geleophysic Dysplasia Type 1.	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 ADAMTSL2 gene"] Parameters [] Preparation ["No fasting required", "No medication adjustments required", "Genetic counselling session required before blood draw"] Indications ["Diagnostic confirmation of Geleophysic Dysplasia Type 1", "Familial screening for Geleophysic Dysplasia Type 1"] Measurement technique Confirm with laboratory Codes LOINC: 91854-6 ICD-10: Q87.8 Clinical summary This genetic test analyzes the ADAMTSL2 gene to identify pathogenic variants associated with Geleophysic Dysplasia Type 1.
TEST-3613 ADAMTSL4 Gene Ectopia Lentis (Isolated, Autosomal Recessive) Genetic Test This diagnostic test evaluates the ADAMTSL4 gene for pathogenic variants associated with isolated autosomal recessive ectopia lentis.	Whole Blood (Peripheral Venipuncture)	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ADAMTSL4 gene sequence", "Copy Number Variants (CNVs) within ADAMTSL4"] Parameters [] Preparation ["Mandatory pre-test genetic counselling session required."] Indications ["Clinical suspicion of isolated ectopia lentis", "Family history of ectopia lentis"] Measurement technique Confirm with laboratory Codes LOINC: 76751-6 ICD-10: Q12.1, H27.1 Clinical summary This diagnostic test evaluates the ADAMTSL4 gene for pathogenic variants associated with isolated autosomal recessive ectopia lentis.
TEST-3728 ADAR Gene Aicardi-Goutières Syndrome Type 6 Genetic Test This genetic test identifies pathogenic variants within the ADAR gene, confirming the diagnosis of Aicardi-Goutières syndrome type 6.	Peripheral whole blood (2 mL EDTA)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ADAR gene sequence", "Pathogenic variants in ADAR gene"] Parameters [] Preparation [] Indications ["Suspected Aicardi-Goutières syndrome type 6", "Elevated CSF interferon-alpha", "Negative TORCH screen", "Family history of Aicardi-Goutières syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 82299-8 ICD-10: G93.41 Clinical summary This genetic test identifies pathogenic variants within the ADAR gene, confirming the diagnosis of Aicardi-Goutières syndrome type 6.
TEST-4866 ADAT3 Gene Intellectual Disability (Autosomal Recessive Type 36) Genetic Test This genetic test identifies pathogenic variants in the ADAT3 gene, which are responsible for causing autosomal recessive intellectual disability type 36.	Peripheral whole blood (EDTA tube)	3–4 weeks (21–28 calendar days)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ADAT3 gene", "Coverage of ADAT3 exons ±20 bp flanking introns"] Parameters [] Preparation ["No fasting required", "No medication changes needed", "Bring previous neurological reports"] Indications ["Diagnosis of autosomal recessive intellectual disability type 36 (MRT36)", "Genetic counseling for families with affected individuals"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: F78.A1 Clinical summary This genetic test identifies pathogenic variants in the ADAT3 gene, which are responsible for causing autosomal recessive intellectual disability type 36.
TEST-4035 ADD2 Gene Hypertension Genetic Test This test identifies DNA variants in the adducin beta gene that increase your lifelong risk of developing essential hypertension.	Whole blood (peripheral)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ADD2 gene variants (SNVs, indels, CNVs)", "Germline mutations affecting renal sodium handling and vascular tone"] Parameters [] Preparation ["Complete mandatory pre-genetic counselling session", "Sign informed consent", "Provide detailed clinical history of hypertension diagnoses and current medications", "No fasting required"] Indications ["Individuals with a family history of hypertension", "Proactive genomic wellness insights", "Personalised antihypertensive choice", "Family screening"] Measurement technique Confirm with laboratory Codes LOINC: 48018-6 ICD-10: I10 Clinical summary This test identifies DNA variants in the adducin beta gene that increase your lifelong risk of developing essential hypertension.
TEST-2416 ADGRG1 Gene Polymicrogyria Bilateral Frontoparietal Genetic Test This test detects pathogenic variants in the ADGRG1 gene associated with bilateral frontoparietal polymicrogyria.	Blood on 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 ADGRG1 gene", "Single nucleotide variants", "Small insertions/deletions", "Copy number changes"] Parameters [] Preparation ["Mandatory clinical history review and genetic counselling session prior to sample collection", "Detailed pedigree analysis required"] Indications ["Patients with clinical or radiological suspicion of bilateral frontoparietal polymicrogyria"] Measurement technique Confirm with laboratory Codes LOINC: 98066-7 ICD-10: Q04.3, Z13.71, Z14.8 Clinical summary This test detects pathogenic variants in the ADGRG1 gene associated with bilateral frontoparietal polymicrogyria.
TEST-4412 ADGRV1 Gene Febrile Seizures, Familial, Type 4 Genetic Test This test identifies pathogenic mutations in the ADGRV1 gene associated with familial febrile seizures type 4.	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 mutations in the ADGRV1 gene"] Parameters [] Preparation ["No fasting required", "Continue prescribed medications unless advised otherwise by a doctor"] Indications ["Diagnosis of familial febrile seizures type 4", "Risk assessment for recurrence in family members", "Guiding clinical management"] Measurement technique Confirm with laboratory Codes LOINC: 94086-1 ICD-10: R56.0 Clinical summary This test identifies pathogenic mutations in the ADGRV1 gene associated with familial febrile seizures type 4.
TEST-6222 ADK Gene Hypermethioninemia due to Adenosine Kinase Deficiency Test This genetic test identifies pathogenic variants in the adenosine kinase (ADK) gene, confirming a diagnosis of hypermethioninemia due to adenosine kinase deficiency.	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 ADK gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any relevant medications"] Indications ["Suspected hypermethioninemia due to adenosine kinase deficiency", "Confirmation of biochemical findings"] Measurement technique Confirm with laboratory Codes LOINC: 81315-5 ICD-10: E72.11 Clinical summary This genetic test identifies pathogenic variants in the adenosine kinase (ADK) gene, confirming a diagnosis of hypermethioninemia due to adenosine kinase deficiency.
TEST-4932 ADNP Gene Genetic Test for Mental Retardation (Autosomal Dominant Type 28) This test evaluates the ADNP gene for pathogenic variants associated with autosomal dominant intellectual disability (Helsmoortel‑van der Aa syndrome). It identifies mutations that...	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 ADNP gene", "Single nucleotide variants (SNVs)", "Small insertions and deletions (indels)"] Parameters [{"name": "ADNP Gene Variants", "reference_range": "Negative (No pathogenic variants detected)"}] Preparation ["No specific fasting required", "No special medication or diet restrictions"] Indications ["Children and adults with unexplained developmental delay", "Individuals with features suggestive of Helsmoortel‑van der Aa syndrome", "Family members of individuals with known ADNP mutations"] Measurement technique Confirm with laboratory Codes LOINC: 91847-4 ICD-10: F79 Clinical summary This test evaluates the ADNP gene for pathogenic variants associated with autosomal dominant intellectual disability (Helsmoortel‑van der Aa syndrome). It identifies mutations that can cause developmental delays and distinctive physical features.

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.

Before booking

Use the test details as a conversation starter

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.

Explore this area

Genetics tests in Dubai & UAE

Genetics test prices

Genetics: overview

Use the test details as a conversation starter

Related Genetics categories