Genetic Sequencing tests in Dubai & UAE

Compare available Genetic Sequencing 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

256

Listed price range

2,600.00–5,000.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

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Genetic Sequencing test prices

Showing 181–195 of 256 matching tests.

Genetic Sequencing diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-6327 PHKG2 Gene (Glycogen Storage Disease Type IXc) Genetic Test This genetic test identifies pathogenic variants in the PHKG2 gene associated with Glycogen Storage Disease Type IXc (GSD IXc).	Peripheral Whole Blood (EDTA tube or FTA card)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PHKG2 gene variants", "Pathogenic mutations", "Copy Number Variants (CNVs)"] Parameters [] Preparation ["No fasting required", "No special preparation needed"] Indications ["Diagnosis of GSD IXc", "Carrier screening", "Family risk stratification", "Asymptomatic siblings of confirmed patients"] Measurement technique Confirm with laboratory Codes LOINC: 92876-8 ICD-10: E74.09 Clinical summary This genetic test identifies pathogenic variants in the PHKG2 gene associated with Glycogen Storage Disease Type IXc (GSD IXc).
TEST-3012 PHOX2B Gene Central Hypoventilation Syndrome (CCHS) with or without Hirschsprung Disease Test This test analyzes the PHOX2B gene to detect mutations associated with Congenital Central Hypoventilation Syndrome (CCHS) and Hirschsprung disease.	Peripheral Whole Blood (EDTA), Extracted DNA, 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 ["PHOX2B gene sequence", "Pathogenic variants (SNVs, indels, CNVs)"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions"] Indications ["Infants, children, and adults with unexplained central hypoventilation", "Individuals with symptoms suggestive of Hirschsprung disease", "Family history of CCHS or Hirschsprung disease"] Measurement technique Confirm with laboratory Codes LOINC: 82305-2 ICD-10: G47.35, Q43.1 Clinical summary This test analyzes the PHOX2B gene to detect mutations associated with Congenital Central Hypoventilation Syndrome (CCHS) and Hirschsprung disease.
TEST-5430 PIGQ Gene Neurodevelopmental Disorder Genetic Test This genetic test evaluates the PIGQ gene for pathogenic variants associated with neurodevelopmental disorders.	Peripheral whole blood	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PIGQ gene coding region variants", "Pathogenic mutations"] Parameters [] Preparation ["No fasting required", "Prior genetic counseling and guardian consent required for minors"] Indications ["Suspected PIGQ-related neurodevelopmental disorder", "Clinical suspicion of epilepsy, intellectual disability, or autism spectrum disorder"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: F88 Clinical summary This genetic test evaluates the PIGQ gene for pathogenic variants associated with neurodevelopmental disorders.
TEST-2605 PIK3R2 Gene Sequencing for Megalencephaly‑Polymicrogyria‑Polydactyly‑Hydrocephalus Syndrome (MPPH) Test This diagnostic test evaluates the PIK3R2 gene for mutations associated with Megalencephaly‑polymicrogyria‑polydactyly‑hydrocephalus syndrome (MPPH). It utilizes whole-gene Next-Ge...	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 ["PIK3R2 gene sequence", "Copy number variations (CNVs) in PIK3R2"] Parameters [] Preparation ["No specific fasting required", "Inform the phlebotomist of any medications"] Indications ["Suspected diagnosis of MPPH based on clinical features", "Family history of MPPH", "Need for genetic confirmation for prognosis and family planning"] Measurement technique Confirm with laboratory Codes LOINC: 95199-8 ICD-10: Q04.8 Clinical summary This diagnostic test evaluates the PIK3R2 gene for mutations associated with Megalencephaly‑polymicrogyria‑polydactyly‑hydrocephalus syndrome (MPPH). It utilizes whole-gene Next-Generation Sequencing (NGS) with copy-number analysis.
TEST-2782 PKD1L1 Gene Heterotaxy, Visceral Type 8, Autosomal Genetic Test This genetic test analyzes the PKD1L1 gene to detect mutations associated with autosomal recessive visceral heterotaxy type 8 (HTX8). It identifies pathogenic variants causing diso...	Whole Blood	3 – 4 weeks (routine)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PKD1L1 gene sequence", "Pathogenic variants (mutations)", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["No fasting required", "Ensure patient is well-hydrated"] Indications ["Diagnosis of suspected autosomal recessive visceral heterotaxy type 8", "Recurrence risk counseling for families with affected individuals", "Prenatal or preimplantation genetic testing"] Measurement technique Confirm with laboratory Codes LOINC: 93338-0 ICD-10: Q89.3, Q24.8, Z14.8 Clinical summary This genetic test analyzes the PKD1L1 gene to detect mutations associated with autosomal recessive visceral heterotaxy type 8 (HTX8). It identifies pathogenic variants causing disorders of left-right asymmetry and complex congenital heart defects.
TEST-5168 PLEC Gene Sequencing (EBS-PA) Test This test analyzes the PLEC gene to detect mutations associated with Epidermolysis Bullosa Simplex with Pyloric Atresia (EBS-PA).	Whole Blood (EDTA), Extracted Genomic DNA, or FTA Card	22–28 business days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PLEC gene coding region", "Flanking splice sites", "Copy Number Variants (CNV)"] Parameters [] Preparation ["Fasting is not required", "Inform nurse of all medications, especially anticoagulants"] Indications ["Suspected diagnosis of Epidermolysis Bullosa Simplex with Pyloric Atresia (EBS-PA)", "Family history of EBS-PA", "Need for genetic counselling"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: Q81.0, Q40.0 Clinical summary This test analyzes the PLEC gene to detect mutations associated with Epidermolysis Bullosa Simplex with Pyloric Atresia (EBS-PA).
TEST-3537 PRKCSH Gene Polycystic Liver Disease Genetic Test This genetic test identifies pathogenic variants in the PRKCSH gene associated with Autosomal Dominant Polycystic Liver Disease (ADPLD).	Whole Blood (EDTA) or Saliva (Oragene DNA Kit)	21–28 Business Days (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 PRKCSH gene", "Coding region and splice junctions of the PRKCSH gene"] Parameters [] Preparation ["Pre-test genetic counseling session is mandatory", "Provide complete clinical history and prior imaging reports", "Provide a detailed three-generation family pedigree"] Indications ["Suspected Autosomal Dominant Polycystic Liver Disease (ADPLD)", "Family history of ADPLD", "Need for genetic confirmation to guide surveillance and family planning"] Measurement technique Confirm with laboratory Codes LOINC: 88544-6 ICD-10: Q44.6 Clinical summary This genetic test identifies pathogenic variants in the PRKCSH gene associated with Autosomal Dominant Polycystic Liver Disease (ADPLD).
TEST-4225 PRKD1 Gene Congenital Heart Defects and Ectodermal Dysplasia Genetic Test This genetic test evaluates the PRKD1 gene for variants associated with congenital heart defects and ectodermal dysplasia.	Whole Blood (Peripheral), 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 ["PRKD1 gene variants", "DNA sequence analysis"] Parameters [] Preparation ["Clinical history of the patient", "Genetic counselling session with pedigree chart"] Indications ["Personal or family history of congenital heart defects", "Personal or family history of ectodermal dysplasia", "Newborns with ambiguous cardiac findings", "Adults seeking definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 80336-9 ICD-10: Q24.9, Q82.4 Clinical summary This genetic test evaluates the PRKD1 gene for variants associated with congenital heart defects and ectodermal dysplasia.
TEST-2692 PROK2 Gene Kallmann Syndrome Type 4 Genetic Test This genetic test identifies mutations in the PROK2 gene associated with Kallmann syndrome type 4, characterized by hypogonadotropic hypogonadism and anosmia.	Whole blood, extracted DNA, or FTA card blood spot	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DNA sequence variants in the PROK2 gene", "Point mutations", "Small deletions", "Copy number analysis"] Parameters [] Preparation ["No fasting or special preparation is needed"] Indications ["Diagnosis of Kallmann syndrome type 4", "Evaluation of hypogonadotropic hypogonadism with anosmia", "Family planning in affected individuals"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: E23.0 Clinical summary This genetic test identifies mutations in the PROK2 gene associated with Kallmann syndrome type 4, characterized by hypogonadotropic hypogonadism and anosmia.
TEST-5367 PSMB8 Gene Genetic Test for Autoinflammation, Lipodystrophy, and Dermatosis Syndrome This test identifies pathogenic variants in the PSMB8 gene, which are associated with Autoinflammation, Lipodystrophy, and Dermatosis Syndrome (ALDD).	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 PSMB8 gene", "Copy Number Variants (CNVs) in the PSMB8 gene"] Parameters [] Preparation ["No specific fasting required.", "Inform the phlebotomist of any medications being taken."] Indications ["Suspected diagnosis of Autoinflammation, Lipodystrophy, and Dermatosis Syndrome (ALDD)", "Differentiation from other autoinflammatory disorders", "Family counseling for inherited conditions"] Measurement technique Confirm with laboratory Codes LOINC: 21675-8 ICD-10: M04.8 Clinical summary This test identifies pathogenic variants in the PSMB8 gene, which are associated with Autoinflammation, Lipodystrophy, and Dermatosis Syndrome (ALDD).
TEST-6203 PTS Gene Sequencing for BH4-Deficient Hyperphenylalaninemia Type A Test This test identifies disease-causing mutations in the PTS gene responsible for BH4-deficient hyperphenylalaninemia type A.	Whole Blood (EDTA) or 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 PTS gene", "Point mutations", "Copy number variations (CNVs)", "Small indels"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any recent blood transfusions"] Indications ["Suspected BH4-deficient hyperphenylalaninemia type A", "Confirmation of diagnosis", "Guidance for targeted therapy"] Measurement technique Confirm with laboratory Codes LOINC: 21768-8 ICD-10: E70.1 Clinical summary This test identifies disease-causing mutations in the PTS gene responsible for BH4-deficient hyperphenylalaninemia type A.
TEST-2523 PUS1 Gene Mitochondrial Myopathy and Sideroblastic Anemia Type 1 Genetic Test This genetic test identifies pathogenic variants in the PUS1 gene associated with mitochondrial myopathy and sideroblastic anemia type 1 (MLASA1).	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 PUS1 gene", "Single nucleotide substitutions", "Small insertions/deletions", "Copy number variations"] Parameters [] Preparation ["Pre-test genetic counselling session required", "Provide a three-generation family pedigree", "No fasting required", "Avoid vigorous exercise 12 hours before sample collection"] Indications ["Clinical suspicion of mitochondrial myopathy", "Clinical suspicion of sideroblastic anemia type 1 (MLASA1)", "Family history of MLASA1", "Need for definitive diagnosis to guide treatment and management"] Measurement technique Confirm with laboratory Codes LOINC: 98979-8 ICD-10: D64.0, G71.3 Clinical summary This genetic test identifies pathogenic variants in the PUS1 gene associated with mitochondrial myopathy and sideroblastic anemia type 1 (MLASA1).
TEST-2544 QARS1 Gene Sequencing Test (Microcephaly, Progressive Seizures, Cerebral‑Cerebellar Atrophy) This test identifies pathogenic variants in the QARS1 gene associated with microcephaly, progressive seizures, and cerebral-cerebellar atrophy.	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 ["QARS1 gene variants", "Pathogenic mutations"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications"] Indications ["Infants and children with neurodevelopmental delay", "Progressive microcephaly", "Early-onset epilepsy of unknown aetiology"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: Q02, G93.89, G40.819 Clinical summary This test identifies pathogenic variants in the QARS1 gene associated with microcephaly, progressive seizures, and cerebral-cerebellar atrophy.
TEST-5957 RAB3GAP1 Gene Warburg Micro Syndrome Type 1 Genetic Test This test evaluates the RAB3GAP1 gene for pathogenic variants associated with Warburg micro syndrome type 1.	Whole Blood (EDTA) 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 RAB3GAP1 gene", "Single nucleotide variants", "Small insertions/deletions", "Copy number changes"] Parameters [] Preparation ["No dietary or medication changes required", "Mandatory pre-genetic counselling session"] Indications ["Suspected Warburg micro syndrome type 1", "Family history of Warburg micro syndrome type 1", "Genetic counselling for families with affected individuals"] Measurement technique Confirm with laboratory Codes LOINC: 94252-9 ICD-10: Q87.8 Clinical summary This test evaluates the RAB3GAP1 gene for pathogenic variants associated with Warburg micro syndrome type 1.
TEST-2200 RAB3GAP2 Gene (Warburg Micro Syndrome Type 2) NGS Test This test evaluates the RAB3GAP2 gene for pathogenic variants associated with Warburg Micro Syndrome Type 2.	Peripheral whole blood (EDTA), buccal swab, 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 RAB3GAP2 gene", "Single-nucleotide variants (SNVs)", "Small insertions or deletions (indels)"] Parameters [] Preparation ["Maintain all prescribed medications unless directed otherwise by a physician.", "Seek immediate emergency care and postpone sample collection if the patient experiences new-onset seizures, severe feeding difficulties, or respiratory distress."] Indications ["Paediatric dysmorphology evaluations", "Suspected Warburg Micro Syndrome Type 2", "Family history of consanguinity with relevant clinical features"] Measurement technique Confirm with laboratory Codes LOINC: 77907-3 ICD-10: Q87.8 Clinical summary This test evaluates the RAB3GAP2 gene for pathogenic variants associated with Warburg Micro Syndrome Type 2.

Category overview

Genetic Sequencing: overview

Achieving a definitive diagnosis for multi-system or exceptionally rare disorders requires reading the deepest layers of your foundational biological code. As the pinnacle of our advanced Genetics department, Genetic Sequencing (including Whole Exome or Whole Genome testing) provides an incredibly detailed, high-resolution scan of your DNA. By leveraging state-of-the-art Next-Generation Sequencing technology, this expansive molecular screening helps uncover elusive genetic variants that standard tests miss, safely guiding your healthcare provider in tailoring highly personalized medical treatments and opening doors to advanced precision medicine. Consistently trusted for advanced genomic analysis across premier diagnostic labs in Dubai and the UAE, DNA Labs ensures strict patient confidentiality, exceptional analytical precision, and highly efficient reporting. Secure the definitive insights your health requires—book your genetic sequencing testing in UAE, arrange a secure clinical sample collection, or consult our dedicated medical genetics experts.

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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.