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 196–210 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4276 ARX Gene Early Infantile Epileptic Encephalopathy Type 1 Genetic Test This genetic test identifies mutations in the ARX gene associated with Early Infantile Epileptic Encephalopathy Type 1 (EIEE1).	Peripheral Whole Blood (EDTA), Extracted DNA, 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 ["ARX gene sequence", "Copy Number Variants (CNVs) in ARX gene"] Parameters [] Preparation ["No specific fasting required", "Continue prescribed medications unless advised otherwise by physician"] Indications ["Suspected Early Infantile Epileptic Encephalopathy Type 1 (EIEE1)", "Neonatal-onset seizures with developmental delay"] Measurement technique Confirm with laboratory Codes LOINC: 81306-1 ICD-10: G40.4 Clinical summary This genetic test identifies mutations in the ARX gene associated with Early Infantile Epileptic Encephalopathy Type 1 (EIEE1).
TEST-2637 ARX Gene Lissencephaly (X-linked Type 2) NGS Test This test evaluates the ARX gene for pathogenic variants associated with X-linked lissencephaly type 2 and related brain malformations.	Peripheral Whole Blood or Dried Blood Spot (FTA Card)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ARX gene pathogenic variants", "Nucleotide substitutions", "Small indels", "Copy number variations"] Parameters [] Preparation [] Indications ["Male infants with lissencephaly", "Infantile spasms", "Developmental delay confirmed by brain MRI"] Measurement technique Confirm with laboratory Codes LOINC: 94243-9 ICD-10: Q04.3 Clinical summary This test evaluates the ARX gene for pathogenic variants associated with X-linked lissencephaly type 2 and related brain malformations.
TEST-5541 ARX Gene Partington Syndrome Genetic Test This test sequences the ARX gene to detect pathogenic variants associated with Partington syndrome.	Peripheral Whole Blood (3-5 mL in EDTA) 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 ["ARX gene sequence", "Pathogenic variants in ARX gene"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of all current medications"] Indications ["Suspected ARX-related Partington syndrome", "X-linked intellectual disability", "Family history of Partington syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 10386-3 ICD-10: Q87.8 Clinical summary This test sequences the ARX gene to detect pathogenic variants associated with Partington syndrome.
TEST-4525 ARX Gene Sequencing (Hydranencephaly with Abnormal Genitalia / X‑Linked Lissencephaly Type 2) Genetic Test This genetic test sequences the ARX gene to identify pathogenic variants associated with specific neurodevelopmental disorders.	Whole blood, extracted DNA, or one drop on FTA card	3 to 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ARX gene sequence", "Pathogenic variants (SNPs, indels, CNVs)"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any medications"] Indications ["Suspected ARX-related disorders", "Diagnosis confirmation", "Prognosis determination", "Family planning"] Measurement technique Confirm with laboratory Codes LOINC: 21641-2 ICD-10: Q04.2, Q04.8, Q87.0 Clinical summary This genetic test sequences the ARX gene to identify pathogenic variants associated with specific neurodevelopmental disorders.
TEST-2937 ARX Gene-Associated Agenesis of Corpus Callosum with Abnormal Genitalia (XLAG) Genetic Test This diagnostic test evaluates the ARX gene for pathogenic variants associated with X-linked lissencephaly with ambiguous genitalia (XLAG) syndrome and related neurological conditi...	Peripheral whole blood (3–5 mL venipuncture) or finger-prick 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 ARX gene", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)", "Intragenic Copy Number Variants (CNVs)"] Parameters [] Preparation ["No specific fasting required", "Continue all prescribed medications unless advised otherwise by your doctor"] Indications ["Individuals with clinical features suggestive of XLAG syndrome", "Family screening for ARX-related disorders", "Prenatal or preimplantation genetic diagnosis options"] Measurement technique Confirm with laboratory Codes LOINC: 80230-8 ICD-10: Q04.0 Clinical summary This diagnostic test evaluates the ARX gene for pathogenic variants associated with X-linked lissencephaly with ambiguous genitalia (XLAG) syndrome and related neurological conditions.
TEST-5731 ASAH1 Gene Sequencing for Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy (SMA-PME) Test This test detects pathogenic variants in the ASAH1 gene associated with Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy (SMA-PME).	Whole Blood (EDTA), 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 ASAH1 gene", "Copy Number Variations (CNV) in the ASAH1 gene"] Parameters [] Preparation ["No specific fasting required", "No medication adjustments needed prior to sample collection"] Indications ["Suspected diagnosis of SMA-PME", "Patients with hallmark symptoms of myoclonus and motor regression"] Measurement technique Confirm with laboratory Codes LOINC: 81260-9 ICD-10: G12.1, G40.3 Clinical summary This test detects pathogenic variants in the ASAH1 gene associated with Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy (SMA-PME).
TEST-3994 ASCL1 Gene Central Hypoventilation Syndrome (Congenital) Genetic Test This test identifies pathogenic variants in the ASCL1 gene associated with Congenital Central Hypoventilation Syndrome (CCHS). It uses Next-Generation Sequencing (NGS) for comprehe...	Whole Blood (EDTA), Extracted DNA, or FTA Card Blood Spot	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 ASCL1 gene", "Single nucleotide variants (SNVs)", "Small insertions or deletions (indels)", "Large copy number variants (deletions/duplications)"] Parameters [] Preparation ["No fasting required", "No medication adjustments required"] Indications ["Clinical suspicion of Congenital Central Hypoventilation Syndrome (CCHS)", "Individuals with unexplained alveolar hypoventilation or autonomic dysregulation"] Measurement technique Confirm with laboratory Codes LOINC: 94219-7 ICD-10: G47.69 Clinical summary This test identifies pathogenic variants in the ASCL1 gene associated with Congenital Central Hypoventilation Syndrome (CCHS). It uses Next-Generation Sequencing (NGS) for comprehensive analysis.
TEST-3001 ASCL1 Gene Central Hypoventilation Syndrome, Congenital Test This diagnostic test evaluates the ASCL1 gene for pathogenic variants associated with Congenital Central Hypoventilation Syndrome (CCHS). It identifies disease-causing mutations li...	Whole Blood (EDTA), Extracted DNA, FTA Card (One Drop)	3 to 4 Weeks (Expedited Processing Available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ASCL1 gene", "Full coding exons and flanking intronic regions of ASCL1"] Parameters [{"name": "Analytical Sensitivity", "reference_range": "99.9%"}, {"name": "Analytical Specificity", "reference_range": "99.9%"}, {"name": "Mean Read Depth", "reference_range": "100x"}] Preparation ["No specific fasting required", "Inform laboratory of any medications that may compromise DNA integrity"] Indications ["Suspected Congenital Central Hypoventilation Syndrome (CCHS)", "Neonates and paediatric patients with abnormal respiratory control", "Family planning decisions related to CCHS risk"] Measurement technique Confirm with laboratory Codes LOINC: 92824-5 ICD-10: G47.35 Clinical summary This diagnostic test evaluates the ASCL1 gene for pathogenic variants associated with Congenital Central Hypoventilation Syndrome (CCHS). It identifies disease-causing mutations linked to Ondine's Curse.
TEST-2558 ASPM Gene Microcephaly Autosomal Recessive Type 5 Genetic Test This genetic test identifies pathogenic variants in the ASPM gene associated with autosomal recessive primary microcephaly type 5 (MCPH5). It utilizes next-generation sequencing (N...	Peripheral whole blood (EDTA), extracted genomic 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 ["Pathogenic variants in the ASPM gene", "Single-nucleotide variants (SNVs)", "Copy-number variations (CNVs)"] Parameters [{"name": "ASPM Gene Variants", "reference_range": "No pathogenic variants detected"}] Preparation ["No specific fasting required", "Inform phlebotomist of any bleeding disorders or medications"] Indications ["Clinical suspicion of autosomal recessive primary microcephaly type 5 (MCPH5)", "Family history of MCPH5", "Genetic counselling for families with microcephaly"] Measurement technique Confirm with laboratory Codes LOINC: 94809-4 ICD-10: Q02 Clinical summary This genetic test identifies pathogenic variants in the ASPM gene associated with autosomal recessive primary microcephaly type 5 (MCPH5). It utilizes next-generation sequencing (NGS) to detect single-nucleotide variants and copy-number variations.
TEST-6212 ASS1 Gene Citrullinemia Genetic Test This test identifies mutations in the ASS1 gene associated with citrullinemia type I, a urea cycle disorder.	Whole blood (EDTA) or FTA card (dried blood spot)	3 to 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ASS1 gene pathogenic variants", "Urea cycle disorder risk"] Parameters [] Preparation ["Do not discontinue prescribed treatments", "Inform physician of recent blood transfusions"] Indications ["Suspected citrullinemia type I", "Family history of urea cycle disorders", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 76016-2 ICD-10: E72.2 Clinical summary This test identifies mutations in the ASS1 gene associated with citrullinemia type I, a urea cycle disorder.
TEST-3671 Ataxia Genetic Test) This test identifies genetic mutations associated with various forms of hereditary ataxia.	Whole blood (EDTA), extracted DNA, or dried blood spot (FTA card)	3–4 Weeks	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in ataxia-related genes", "Copy Number Variations (CNVs) in ataxia-related genes"] Parameters [] Preparation ["Fasting is not required", "Provide a list of current medications and supplements", "No supplements or drugs need to be discontinued"] Indications ["Diagnosis of suspected hereditary ataxia", "Predictive testing for individuals with family history", "Carrier screening", "Family risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 92195-6 ICD-10: G11.9, G11.0, G11.1, G11.2, G11.3, G11.4, G11.8 Clinical summary This test identifies genetic mutations associated with various forms of hereditary ataxia.
TEST-3696 Ataxia Repeat Expansion Panel (Genetic Test) This test detects pathogenic repeat expansions in genes linked to hereditary ataxias.	Peripheral whole blood (EDTA) or FTA card	3–4 Weeks	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic repeat expansions", "Gene mutations associated with ataxia"] Parameters [] Preparation ["No fasting required", "No medication adjustments needed"] Indications ["Suspected hereditary ataxia", "Family history of ataxia", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 92857-7 ICD-10: G11.0, G11.1, G11.2, G11.3, G11.4, G11.8, G11.9 Clinical summary This test detects pathogenic repeat expansions in genes linked to hereditary ataxias.
TEST-2727 Ataxia-Telangiectasia Genetic Testing (NGS with Sanger Confirmation) Test This test identifies pathogenic variants in the ATM gene, confirming a diagnosis of Ataxia-Telangiectasia.	Peripheral whole blood (Lavender-top EDTA tubes)	40 working days	2,600.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ATM gene variants", "Single-nucleotide variants", "Small insertions/deletions", "Exon-level copy-number changes"] Parameters [] Preparation ["Do not discontinue prescribed therapy without physician instruction", "Testing in children requires prior clinical assessment by a specialist"] Indications ["Suspected Ataxia-Telangiectasia", "Progressive cerebellar ataxia", "Immunodeficiency", "Elevated cancer risk"] Measurement technique Confirm with laboratory Codes LOINC: 92041-1 ICD-10: G11.3 Clinical summary This test identifies pathogenic variants in the ATM gene, confirming a diagnosis of Ataxia-Telangiectasia.
TEST-5741 Ataxin-10 (ATXN10) Gene Spinocerebellar Ataxia Type 10 Autosomal Dominant Genetic Test This genetic test identifies the specific pentanucleotide repeat expansion in the ATXN10 gene associated with Spinocerebellar Ataxia Type 10 (SCA10).	Whole blood (3–5 mL in EDTA), 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 ["ATXN10 gene pentanucleotide repeat expansion", "Pathogenic variant detection"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Clinical suspicion of hereditary ataxia", "Confirmed family history of SCA10", "Genetic counseling for at-risk individuals"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: G11.2 Clinical summary This genetic test identifies the specific pentanucleotide repeat expansion in the ATXN10 gene associated with Spinocerebellar Ataxia Type 10 (SCA10).
TEST-6072 ATIC Gene AICA-Ribosiduria due to ATIC Deficiency Genetic Test This genetic test identifies pathogenic variants in the ATIC gene associated with AICA-ribosiduria, an autosomal recessive disorder of purine metabolism.	Whole Blood (EDTA) 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 ["Pathogenic variants in the ATIC gene"] Parameters [] Preparation ["Mandatory genetic counselling session", "Provide complete clinical history", "No fasting required"] Indications ["Diagnosis of AICA-ribosiduria", "Carrier screening for AICA-ribosiduria", "Prenatal diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: E79.8 Clinical summary This genetic test identifies pathogenic variants in the ATIC gene associated with AICA-ribosiduria, an autosomal recessive disorder of purine metabolism.

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

Genetics test prices

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