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 226–240 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5274 ATP6V0A2 Gene Sequencing for Autosomal Recessive Cutis Laxa Type 2A Test This test identifies pathogenic variants in the ATP6V0A2 gene, confirming a diagnosis of autosomal recessive cutis laxa type 2A.	Peripheral Whole Blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ATP6V0A2 gene variants", "Pathogenic mutations"] Parameters [] Preparation ["Pre-test genetic counselling is mandatory"] Indications ["Suspected autosomal recessive cutis laxa type 2A", "Family history of cutis laxa type 2A", "Carrier testing for family planning"] Measurement technique Confirm with laboratory Codes LOINC: 94805-5 ICD-10: Q82.8 Clinical summary This test identifies pathogenic variants in the ATP6V0A2 gene, confirming a diagnosis of autosomal recessive cutis laxa type 2A.
TEST-4465 ATP6V0A2 Gene Wrinkly Skin Syndrome Genetic Test This genetic test analyzes the ATP6V0A2 gene to identify pathogenic variants associated with wrinkly skin syndrome.	Blood, DNA FTA Card, Extracted DNA	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ATP6V0A2 gene sequence", "Single-nucleotide variants", "Small insertions/deletions", "Copy-number variants (CNVs)"] Parameters [] Preparation ["No fasting required.", "Providing a clinical history and a genetic counseling pedigree chart is recommended."] Indications ["Diagnosis of wrinkly skin syndrome", "Carrier screening for family planning"] Measurement technique Confirm with laboratory Codes LOINC: 21665-9 ICD-10: Q82.8 Clinical summary This genetic test analyzes the ATP6V0A2 gene to identify pathogenic variants associated with wrinkly skin syndrome.
TEST-3496 ATP6V0A4 Gene Distal Renal Tubular Acidosis (Autosomal Recessive) NGS Test This test identifies pathogenic variants in the ATP6V0A4 gene associated with autosomal recessive distal renal tubular acidosis.	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 ["ATP6V0A4 gene sequence", "Pathogenic variants"] Parameters [] Preparation ["Mandatory pre-test genetic counselling", "Provide list of all prescribed drugs and supplements", "Avoid recent blood transfusion ( Indications ["Suspected autosomal recessive distal renal tubular acidosis", "Family history of dRTA", "Unexplained metabolic acidosis"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: N25.89 Clinical summary This test identifies pathogenic variants in the ATP6V0A4 gene associated with autosomal recessive distal renal tubular acidosis.
TEST-3536 ATP6V1B1 Gene Renal Tubular Acidosis with Deafness Genetic Test This test identifies pathogenic variants in the ATP6V1B1 gene associated with distal renal tubular acidosis and sensorineural deafness.	Whole blood (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 ["ATP6V1B1 gene variants", "Pathogenic mutations"] Parameters [] Preparation ["No fasting required", "Provide detailed medical history and list of current medications"] Indications ["Confirmation of clinical suspicion of dRTA with deafness", "Carrier testing", "Prenatal diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: N25.89 Clinical summary This test identifies pathogenic variants in the ATP6V1B1 gene associated with distal renal tubular acidosis and sensorineural deafness.
TEST-3679 ATP7A Gene Menkes Disease Genetic Test This genetic test evaluates the ATP7A gene for mutations associated with Menkes disease.	Peripheral Whole Blood (also accepted: Dried Blood Spot on FTA card)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ATP7A gene sequence", "Mutations within the ATP7A gene"] Parameters [] Preparation ["No specific fasting required.", "Inform the lab of any relevant family history."] Indications ["Suspected Menkes disease based on clinical presentation", "Family history of Menkes disease", "Need for definitive genetic diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 101717-5 ICD-10: E83.0, Z13.79, Z84.81 Clinical summary This genetic test evaluates the ATP7A gene for mutations associated with Menkes disease.
TEST-5395 ATP7A Gene Occipital Horn Syndrome Genetic Test This test identifies pathogenic variants in the ATP7A gene associated with Occipital Horn Syndrome (OHS).	Peripheral Blood (EDTA), Extracted DNA, FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ATP7A gene sequence", "Single nucleotide variants (SNVs)", "Insertions/Deletions (Indels)", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["No fasting required", "Mandatory pre-test genetic counseling session"] Indications ["Suspected Occipital Horn Syndrome (OHS)", "Family history of OHS", "Carrier testing for at-risk family members", "Differential diagnosis of copper transport disorders"] Measurement technique Confirm with laboratory Codes LOINC: 81247-8 ICD-10: E83.0 Clinical summary This test identifies pathogenic variants in the ATP7A gene associated with Occipital Horn Syndrome (OHS).
TEST-5835 ATP7A Gene Spinal Muscular Atrophy, Distal, X-linked DNA Test (NGS) This diagnostic test evaluates the ATP7A gene for pathogenic variants associated with X-linked distal spinal muscular atrophy (SMAX2). It identifies single nucleotide variants, sma...	Peripheral 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 ["ATP7A gene sequence", "Copy Number Variants (CNVs) in ATP7A gene"] Parameters [] Preparation ["No specific fasting required", "Inform the lab of any recent blood transfusions ( Indications ["Suspected diagnosis of X-linked distal spinal muscular atrophy (SMAX2)", "Family history of SMAX2", "Carrier screening for at-risk female relatives", "Family planning and reproductive counseling"] Measurement technique Confirm with laboratory Codes LOINC: 82335-1 ICD-10: G12.9 Clinical summary This diagnostic test evaluates the ATP7A gene for pathogenic variants associated with X-linked distal spinal muscular atrophy (SMAX2). It identifies single nucleotide variants, small insertions/deletions, and copy number changes.
TEST-4021 ATP8A2 Gene Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome Type 4 (CAMRQ4) Genetic Test This genetic test evaluates the ATP8A2 gene for pathogenic variants associated with Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome Type 4 (CAMRQ4).	Peripheral whole blood (EDTA) 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 ATP8A2 gene", "Coding region sequence analysis"] Parameters [] Preparation ["Mandatory genetic counselling session", "No fasting required", "No medication adjustment needed"] Indications ["Individuals with clinical features suggestive of CAMRQ4", "Family history of CAMRQ4", "Differential diagnosis of cerebellar ataxia and intellectual disability"] Measurement technique Confirm with laboratory Codes LOINC: 81313-4 ICD-10: G11.8 Clinical summary This genetic test evaluates the ATP8A2 gene for pathogenic variants associated with Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome Type 4 (CAMRQ4).
TEST-6206 ATP8B1 Gene Intrahepatic Cholestasis of Pregnancy Type 1 (ICP1) Genetic Test This test evaluates the ATP8B1 gene for pathogenic variants associated with intrahepatic cholestasis of pregnancy type 1 (ICP1) and progressive familial intrahepatic cholestasis ty...	Whole Blood (Peripheral Venous 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 ATP8B1 gene", "Single-nucleotide variants (SNVs)", "Insertions/Deletions (Indels)", "Copy-number changes"] Parameters [] Preparation ["No fasting or dietary changes required", "Follow obstetrician’s guidance for any concurrent blood work", "Do not discontinue prescribed medication without consulting your doctor"] Indications ["Women with personal or family history of severe pregnancy itching", "Women with elevated bile acids during pregnancy", "Women diagnosed with ICP", "Assessment of recurrence risk and family planning"] Measurement technique Confirm with laboratory Codes LOINC: 10118-6 ICD-10: O26.619, Z14.8, Z31.430 Clinical summary This test evaluates the ATP8B1 gene for pathogenic variants associated with intrahepatic cholestasis of pregnancy type 1 (ICP1) and progressive familial intrahepatic cholestasis type 1 (PFIC1).
TEST-6199 ATP8B1 Gene Progressive Familial Intrahepatic Cholestasis Type 1 (PFIC1) Genetic Test This genetic test evaluates the ATP8B1 gene for pathogenic variants associated with Progressive Familial Intrahepatic Cholestasis Type 1 (PFIC1). It helps confirm the diagnosis and...	Peripheral blood, 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 ATP8B1 gene", "Presence of mutations causing PFIC1"] Parameters [] Preparation ["No specific fasting required", "No need to stop prescribed medications unless advised by a physician"] Indications ["Diagnosis of PFIC1 in individuals with suggestive clinical features", "Carrier screening for family members", "Prenatal diagnosis", "Genetic counselling"] Measurement technique Confirm with laboratory Codes LOINC: 21638-4 ICD-10: K76.81 Clinical summary This genetic test evaluates the ATP8B1 gene for pathogenic variants associated with Progressive Familial Intrahepatic Cholestasis Type 1 (PFIC1). It helps confirm the diagnosis and guide management of this severe liver disorder.
TEST-6107 ATP8B1 Gene Sequencing for Benign Recurrent Intrahepatic Cholestasis (BRIC) Test This test identifies pathogenic variants in the ATP8B1 gene associated with benign recurrent intrahepatic cholestasis (BRIC).	Peripheral blood (EDTA whole blood)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ATP8B1 gene variants", "Pathogenic mutations"] Parameters [] Preparation ["No fasting required", "Completed clinical history form needed", "Pre-genetic counselling session required"] Indications ["Suspected benign recurrent intrahepatic cholestasis (BRIC)", "Family history of BRIC"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: K76.89 Clinical summary This test identifies pathogenic variants in the ATP8B1 gene associated with benign recurrent intrahepatic cholestasis (BRIC).
TEST-2359 ATR Gene Seckel Syndrome Type 1 Next-Generation Sequencing (Genetic Test This genetic test identifies pathogenic variants in the ATR gene associated with Seckel syndrome type 1.	Whole 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 ["Pathogenic single nucleotide variants (SNVs)", "Small insertions or deletions (indels)", "Exon-level copy number changes (CNVs)"] Parameters [] Preparation ["No special preparation such as fasting is required.", "Stay well hydrated before collection."] Indications ["Suspected Seckel syndrome type 1", "Family history of Seckel syndrome type 1", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 81267-6 ICD-10: Q87.1 Clinical summary This genetic test identifies pathogenic variants in the ATR gene associated with Seckel syndrome type 1.
TEST-2348 ATRIP Gene Seckel Syndrome Genetic Test This genetic test detects pathogenic variants in the ATRIP gene associated with Seckel syndrome.	Peripheral Blood, Extracted DNA, 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 ["Pathogenic variants in the ATRIP gene"] Parameters [] Preparation [] Indications ["Clinical suspicion of Seckel syndrome", "Evaluation of dysmorphology", "Genetic counseling"] Measurement technique Confirm with laboratory Codes LOINC: 92895-0 ICD-10: Q87.1 Clinical summary This genetic test detects pathogenic variants in the ATRIP gene associated with Seckel syndrome.
TEST-4787 ATRX Gene (X‑Linked Intellectual Disability with Hypotonic Facies Syndrome) Genetic Test This test identifies pathogenic variants, including single-nucleotide variants, indels, and copy-number changes, within the entire coding region of the ATRX gene.	Whole Blood (EDTA) 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 ["Single-nucleotide variants (SNVs)", "Insertions/Deletions (Indels)", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["No fasting required", "Do not discontinue prescribed medication without consulting a doctor"] Indications ["Suspected X-linked intellectual disability with hypotonic facies syndrome", "Neurodevelopmental disorders with unknown etiology"] Measurement technique Confirm with laboratory Codes LOINC: 96536-3 ICD-10: Q87.8 Clinical summary This test identifies pathogenic variants, including single-nucleotide variants, indels, and copy-number changes, within the entire coding region of the ATRX gene.
TEST-3759 ATRX Gene Alpha-Thalassemia/Mental Retardation Syndrome Genetic Test This test evaluates the ATRX gene for pathogenic variants associated with Alpha-Thalassemia/Mental Retardation Syndrome (ATR-X). It uses Next-Generation Sequencing (NGS) with Copy...	Whole Blood (EDTA) or Saliva (Oragene)	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 ATRX gene", "Copy Number Variants (CNVs) in the ATRX gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of current anticoagulant use"] Indications ["Suspected Alpha-Thalassemia/Mental Retardation Syndrome (ATR-X)", "Family history of ATR-X", "Evaluation of intellectual disability with associated features"] Measurement technique Confirm with laboratory Codes LOINC: 81663-8 ICD-10: Q87.8, D56.0, Z13.7 Clinical summary This test evaluates the ATRX gene for pathogenic variants associated with Alpha-Thalassemia/Mental Retardation Syndrome (ATR-X). It uses Next-Generation Sequencing (NGS) with Copy Number Variant (CNV) analysis.

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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