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

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Genetics test prices

Showing 2371–2385 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-6388 SLC6A9 Gene Glycine Encephalopathy with Normal Serum Glycine Genetic Test This test identifies disease-causing variants in the SLC6A9 gene associated with glycine encephalopathy, particularly when serum glycine levels are normal.	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 SLC6A9 gene"] Parameters [{"name": "Analytical Sensitivity", "reference_range": ">99%"}] Preparation ["Provide complete clinical history", "Genetic counselling session recommended", "No fasting or medication changes required unless directed by doctor", "Do not collect during acute febrile illness"] Indications ["Suspected glycine encephalopathy with normal serum glycine", "Family history of glycine encephalopathy", "Need for precise molecular diagnosis for management and counselling"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: E72.8, G93.49, Z13.71 Clinical summary This test identifies disease-causing variants in the SLC6A9 gene associated with glycine encephalopathy, particularly when serum glycine levels are normal.
TEST-4997 SLC9A6 Gene Christianson Syndrome (X-linked Intellectual Disability) Genetic Test This genetic test identifies pathogenic variants in the SLC9A6 gene, confirming a diagnosis of Christianson syndrome.	Whole blood (EDTA)	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 SLC9A6 gene", "Copy Number Variations (CNV) in SLC9A6"] Parameters [] Preparation ["No specific patient preparation required"] Indications ["Suspected Christianson syndrome", "X-linked intellectual disability", "Family history of Christianson syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 93101-1 ICD-10: Q87.89 Clinical summary This genetic test identifies pathogenic variants in the SLC9A6 gene, confirming a diagnosis of Christianson syndrome.
TEST-3859 SLC9A9 Gene (Autism Susceptibility, Type 16) Genetic Test This genetic test analyzes the SLC9A9 gene for variants associated with autism susceptibility type 16.	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 SLC9A9 gene", "Single-nucleotide variants (SNVs)", "Insertions and deletions (indels)"] Parameters [] Preparation ["Genetic counseling session required before testing", "Valid referral from a DHA-licensed specialist required", "Legal guardian consent required for minors"] Indications ["Individuals with clinical features suggestive of autism spectrum disorder", "Family history of autism susceptibility type 16", "Genetic counseling for individuals with developmental delays"] Measurement technique Confirm with laboratory Codes LOINC: 81327-5 ICD-10: Z15.09 Clinical summary This genetic test analyzes the SLC9A9 gene for variants associated with autism susceptibility type 16.
TEST-5923 SLITRK1 Gene Tourette Syndrome Genetic Test This test detects pathogenic variants in the SLITRK1 gene associated with Tourette syndrome.	Venous Blood or 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 SLITRK1 gene"] Parameters [] Preparation ["No fasting required", "Avoid heavy physical exertion immediately before sampling", "Pre-test genetic counseling recommended"] Indications ["Diagnosis of Tourette syndrome", "Family risk assessment for Tourette syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 94500-5 ICD-10: F95.2 Clinical summary This test detects pathogenic variants in the SLITRK1 gene associated with Tourette syndrome.
TEST-4396 SLMAP Gene Brugada Syndrome Type 9 Genetic Test This test identifies pathogenic variants in the SLMAP gene, which are associated with Brugada syndrome, a cardiac channelopathy.	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 SLMAP gene", "Single nucleotide variants", "Insertions/deletions", "Splice-site alterations"] Parameters [] Preparation [] Indications ["Diagnosis of Brugada syndrome", "Risk stratification for sudden cardiac death", "Family cascade testing"] Measurement technique Confirm with laboratory Codes LOINC: 94219-6 ICD-10: I49.81 Clinical summary This test identifies pathogenic variants in the SLMAP gene, which are associated with Brugada syndrome, a cardiac channelopathy.
TEST-4803 SLURP1 Gene Mal de Meleda Genetic Test This test identifies pathogenic variants in the SLURP1 gene associated with Mal de Meleda.	Peripheral Whole Blood	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SLURP1 gene pathogenic variants", "Coding exons and flanking regions"] Parameters [] Preparation ["No fasting required", "Avoid blood-thinning medications unless approved by physician"] Indications ["Suspected Mal de Meleda", "Family history of Mal de Meleda", "Need for genetic counselling"] Measurement technique Confirm with laboratory Codes LOINC: 21637-4 ICD-10: Q82.8 Clinical summary This test identifies pathogenic variants in the SLURP1 gene associated with Mal de Meleda.
TEST-6375 SLX4 Gene Fanconi Anemia Type P Genetic Test This genetic test identifies mutations in the SLX4 gene associated with Fanconi anemia type P.	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 ["SLX4 gene sequence", "Single-nucleotide variants", "Small insertion-deletion mutations", "Copy-number aberrations"] Parameters [] Preparation ["Never discontinue or adjust prescribed medications without consulting your treating physician."] Indications ["Individuals with unexplained bone marrow failure", "Individuals with a family history of Fanconi anemia", "Individuals with clinical features suggestive of Fanconi anemia"] Measurement technique Confirm with laboratory Codes LOINC: 93344-3 ICD-10: D61.09 Clinical summary This genetic test identifies mutations in the SLX4 gene associated with Fanconi anemia type P.
TEST-4092 SMAD2 Gene Sequencing for Thoracic Aortic Aneurysm Dissection Test This test evaluates the SMAD2 gene for pathogenic variants associated with inherited thoracic aortic aneurysm and dissection syndromes.	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 SMAD2 gene", "Exon and splice-site coverage"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications without consulting your physician"] Indications ["Individuals with a family history of TAAD", "Young individuals with unexplained aortic dilatation", "Individuals with bicuspid aortic valve"] Measurement technique Confirm with laboratory Codes LOINC: 94037-6 ICD-10: I71.2, Z15.09 Clinical summary This test evaluates the SMAD2 gene for pathogenic variants associated with inherited thoracic aortic aneurysm and dissection syndromes.
TEST-2055 SMAD4 Gene Juvenile Polyposis Syndrome Genetic Test This genetic test identifies pathogenic mutations within the SMAD4 gene associated with Juvenile Polyposis Syndrome.	Peripheral whole blood (3–5 mL EDTA) 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 ["SMAD4 gene pathogenic variants", "Hereditary predisposition to polyposis"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Suspected Juvenile Polyposis Syndrome", "Family history of JPS", "Personal history of multiple hamartomatous polyps"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q85.09 Clinical summary This genetic test identifies pathogenic mutations within the SMAD4 gene associated with Juvenile Polyposis Syndrome.
TEST-2525 SMAD4 Gene Myhre Syndrome Genetic Test This test analyzes the entire SMAD4 gene using Next-Generation Sequencing (NGS) to detect pathogenic variants associated with Myhre syndrome.	Peripheral Whole Blood (EDTA) or Derived 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 the SMAD4 gene", "Full gene coverage including intronic and splice-site regions"] Parameters [] Preparation [] Indications ["Children presenting with features suggestive of Myhre syndrome", "Individuals with a family history of Myhre syndrome", "Atypical connective tissue disorders"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q87.8 Clinical summary This test analyzes the entire SMAD4 gene using Next-Generation Sequencing (NGS) to detect pathogenic variants associated with Myhre syndrome.
TEST-2030 SMAD4 Gene Test (Juvenile Polyposis & HHT) NGS DNA Sequencing This test identifies pathogenic variants in the SMAD4 gene associated with Juvenile Polyposis Syndrome (JPS) and Hereditary Hemorrhagic Telangiectasia (HHT).	Peripheral Blood, 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 ["Germline pathogenic variants in the SMAD4 gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any recent blood transfusions or chemotherapy"] Indications ["Individuals with clinical features suggestive of JPS or HHT", "Family history of JPS or HHT", "Pre-symptomatic testing in at-risk individuals"] Measurement technique Confirm with laboratory Codes LOINC: 21645-8 ICD-10: K63.5, I78.0 Clinical summary This test identifies pathogenic variants in the SMAD4 gene associated with Juvenile Polyposis Syndrome (JPS) and Hereditary Hemorrhagic Telangiectasia (HHT).
TEST-4046 SMAD6 Gene Aortic Valve Disease Type 2 Test This genetic test evaluates the SMAD6 gene for variants associated with aortic valve disease type 2 and thoracic aortic aneurysms.	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 SMAD6 gene", "Full gene coverage including exons, splice sites, and indels"] Parameters [] Preparation [] Indications ["Individuals with a family history of bicuspid aortic valve", "Individuals with a family history of early aortic dissection", "Individuals with a family history of related aortopathies"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: I35.9 Clinical summary This genetic test evaluates the SMAD6 gene for variants associated with aortic valve disease type 2 and thoracic aortic aneurysms.
TEST-4790 SMARCA1 Gene X‑Linked Mental Retardation Genetic Test This test identifies pathogenic variants within the SMARCA1 gene associated with X-linked intellectual disability.	Peripheral whole blood, 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 SMARCA1 gene", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variants (CNVs)"] Parameters [] Preparation [] Indications ["Confirmatory diagnosis of X-linked intellectual disability", "Carrier testing", "Family planning"] Measurement technique Confirm with laboratory Codes LOINC: 94727-5 ICD-10: Q99.8 Clinical summary This test identifies pathogenic variants within the SMARCA1 gene associated with X-linked intellectual disability.
TEST-2517 SMARCA2 Gene Nicolaides-Baraitser Syndrome Genetic Test This test identifies pathogenic variants in the SMARCA2 gene associated with Nicolaides-Baraitser syndrome.	Peripheral Whole Blood (EDTA) or Extracted Genomic DNA	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SMARCA2 gene coding regions", "SMARCA2 gene conserved splice sites"] Parameters [] Preparation ["No special preparation such as fasting is required", "Ensure child is well-hydrated"] Indications ["Suspected Nicolaides-Baraitser syndrome based on clinical features", "Family counseling for NCBRS"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q87.1 Clinical summary This test identifies pathogenic variants in the SMARCA2 gene associated with Nicolaides-Baraitser syndrome.
TEST-4912 SMARCA4-Related Intellectual Disability (MRD16) Genetic Test This test detects genetic variants in the SMARCA4 gene associated with intellectual disability.	Peripheral whole blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SMARCA4 gene variants (SNVs, Indels, CNVs)", "Chromatin remodeler gene function"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications without consulting a physician"] Indications ["Suspected SMARCA4-related intellectual disability (MRD16)", "Genetic counselling for intellectual disability", "Family history of MRD16"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: F78, Q87.8 Clinical summary This test detects genetic variants in the SMARCA4 gene associated with intellectual disability.

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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