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.

Compare available tests

Genetic Sequencing test prices

Showing 151–165 of 256 matching tests.

Genetic Sequencing diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4967 MBTPS2 Gene IFAP Syndrome Genetic Test This test identifies pathogenic variants in the MBTPS2 gene associated with Ichthyosis Follicularis, Atrichia, and Photophobia (IFAP) syndrome.	Peripheral Blood (3–5 ml) or Buccal Swab	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 MBTPS2 gene", "Single nucleotide variants (SNVs)", "Insertions/Deletions (Indels)", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["No specific fasting required", "No special medication or diet restrictions"] Indications ["Suspected diagnosis of IFAP syndrome based on clinical features", "Family history of IFAP syndrome", "Genetic counseling for affected families", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 82235-8 ICD-10: Q80.3, Q80.8 Clinical summary This test identifies pathogenic variants in the MBTPS2 gene associated with Ichthyosis Follicularis, Atrichia, and Photophobia (IFAP) syndrome.
TEST-3003 MEGF8 Gene Carpenter Syndrome Type 2 Genetic Test This test identifies pathogenic variants in the MEGF8 gene associated with Carpenter syndrome type 2.	Peripheral Whole Blood (3–5 mL in EDTA tube)	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 MEGF8 gene"] Parameters [] Preparation ["No special preparation needed", "Inform phlebotomist of bleeding disorders or medications"] Indications ["Clinical suspicion of Carpenter syndrome type 2", "Genetic counseling", "Family planning"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q87.0 Clinical summary This test identifies pathogenic variants in the MEGF8 gene associated with Carpenter syndrome type 2.
TEST-2679 MGP Gene Keutel Syndrome Genetic Test This genetic test detects pathogenic variants in the MGP gene associated with Keutel syndrome.	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 ["Pathogenic variants in the MGP gene"] Parameters [] Preparation [] Indications ["Suspected Keutel syndrome based on clinical presentation", "Family history of Keutel syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q78.8 Clinical summary This genetic test detects pathogenic variants in the MGP gene associated with Keutel syndrome.
TEST-6033 MMUT Gene Methylmalonic Aciduria Due to Methylmalonyl-CoA Mutase Deficiency Genetic Test This genetic test analyzes the MMUT gene for mutations causing methylmalonic aciduria.	Whole Blood (EDTA), Extracted DNA, or FTA Card	14–21 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the MMUT gene", "Single nucleotide variants", "Small insertions/deletions", "Copy number variations"] Parameters [] Preparation ["No specific fasting required", "Consult physician regarding medication or diet changes"] Indications ["Suspected methylmalonic aciduria", "Family history of methylmalonic aciduria", "Need for carrier testing", "Prenatal planning"] Measurement technique Confirm with laboratory Codes LOINC: 21639-4 ICD-10: E71.110 Clinical summary This genetic test analyzes the MMUT gene for mutations causing methylmalonic aciduria.
TEST-6012 MOCS1 Gene Molybdenum Cofactor Deficiency Type A Genetic Test This genetic test identifies pathogenic variants in the MOCS1 gene to diagnose Molybdenum Cofactor Deficiency Type A.	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 MOCS1 gene"] Parameters [] Preparation ["Pre-test genetic counseling session is mandatory"] Indications ["Symptomatic infants", "At-risk family members", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 94306-0 ICD-10: E83.10 Clinical summary This genetic test identifies pathogenic variants in the MOCS1 gene to diagnose Molybdenum Cofactor Deficiency Type A.
TEST-4610 MPDZ Gene Hydrocephalus, Nonsyndromic, Autosomal Recessive Type 2 Genetic Test This test identifies pathogenic biallelic variants in the MPDZ gene, confirming a diagnosis of autosomal recessive nonsyndromic hydrocephalus type 2.	Whole Blood or Buccal Swab	3–4 weeks (21–28 business days)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the MPDZ gene", "Biallelic mutations"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions"] Indications ["Diagnosis of nonsyndromic autosomal recessive hydrocephalus type 2", "Neurosurgical planning", "Prognosis assessment", "Recurrence risk assessment for families"] Measurement technique Confirm with laboratory Codes LOINC: 96567-0 ICD-10: Q03.9 Clinical summary This test identifies pathogenic biallelic variants in the MPDZ gene, confirming a diagnosis of autosomal recessive nonsyndromic hydrocephalus type 2.
TEST-6333 MRAP Gene Glucocorticoid Deficiency Type 2 Genetic Test This test identifies pathogenic variants in the MRAP gene associated with Familial Glucocorticoid Deficiency Type 2.	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 ["Pathogenic variants in the MRAP gene", "Single-nucleotide variants", "Small insertions/deletions", "Splice-site alterations"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any bleeding disorders"] Indications ["Infants or children with unexplained hypoglycaemia, hyperpigmentation, and recurrent infections", "Suspected isolated glucocorticoid deficiency based on cortisol and ACTH levels", "Carrier detection", "Prenatal counselling"] Measurement technique Confirm with laboratory Codes LOINC: 94122-3 ICD-10: E27.4 Clinical summary This test identifies pathogenic variants in the MRAP gene associated with Familial Glucocorticoid Deficiency Type 2.
TEST-2169 MSX1 Gene (Witkop Syndrome) Genetic Test This genetic test analyzes the MSX1 gene to identify pathogenic variants associated with Witkop syndrome.	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 ["MSX1 gene sequence", "Pathogenic variants (SNVs, indels, CNVs)"] Parameters [] Preparation ["No special preparation required", "Mandatory pre-test genetic counseling"] Indications ["Confirmation of Witkop syndrome diagnosis", "Reproductive risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 91748-0 ICD-10: Q82.4 Clinical summary This genetic test analyzes the MSX1 gene to identify pathogenic variants associated with Witkop syndrome.
TEST-5076 MT-ATP6 Gene Mitochondrial Complex V (ATP Synthase) Deficiency Genetic Test This genetic test analyzes the MT-ATP6 gene for mutations associated with mitochondrial complex V deficiency, Leigh syndrome, and NARP syndrome.	Whole Blood, Extracted DNA, or Dried Blood Spot (DBS) 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 MT-ATP6 gene", "Mitochondrial ATP synthase subunit 6"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Suspected Leigh syndrome", "Suspected NARP syndrome", "Suspected isolated complex V deficiency", "Family history of mitochondrial disorders"] Measurement technique Confirm with laboratory Codes LOINC: 50008-0 ICD-10: G31.82, E88.49 Clinical summary This genetic test analyzes the MT-ATP6 gene for mutations associated with mitochondrial complex V deficiency, Leigh syndrome, and NARP syndrome.
TEST-4181 MT-TS2 Gene MERRF/MELAS Overlap Syndrome Genetic Test This test evaluates the entire MT-TS2 mitochondrial gene for pathogenic variants associated with MERRF/MELAS overlap syndrome.	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 variants in the MT-TS2 gene", "Point mutations", "Small insertions and deletions", "Mosaic variants"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any relevant medications"] Indications ["Suspected MERRF/MELAS overlap syndrome", "Patients with overlapping neurological and metabolic features", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: E88.49, G31.81, E88.41 Clinical summary This test evaluates the entire MT-TS2 mitochondrial gene for pathogenic variants associated with MERRF/MELAS overlap syndrome.
TEST-3826 MT-TY Gene NGS Test for FSGS & Dilated Cardiomyopathy This test evaluates the MT-TY gene for pathogenic variants associated with FSGS and DCM.	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 MT-TY gene", "Mitochondrial tRNA coding region"] Parameters [] Preparation ["No fasting required", "Provide clinical history and completed genetic counselling pedigree"] Indications ["Clinical suspicion of hereditary FSGS", "Clinical suspicion of hereditary dilated cardiomyopathy", "Family history of FSGS or DCM"] Measurement technique Confirm with laboratory Codes LOINC: 101203-9 ICD-10: N04.1, I42.0 Clinical summary This test evaluates the MT-TY gene for pathogenic variants associated with FSGS and DCM.
TEST-5426 MTOR Gene Sequencing for Neurodevelopmental Disorders Test This test analyzes the MTOR gene for pathogenic variants associated with neurodevelopmental disorders.	Whole Blood, 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 MTOR gene", "Coding region of the MTOR gene"] Parameters [] Preparation ["A genetic counselling session and a pedigree chart of family members affected by MTOR-related neurodevelopmental disorders are mandatory before sample collection."] Indications ["Suspected MTOR-related neurodevelopmental disorder", "Clinical indication of a neurodevelopmental disorder"] Measurement technique Confirm with laboratory Codes LOINC: 82309-8 ICD-10: F89 Clinical summary This test analyzes the MTOR gene for pathogenic variants associated with neurodevelopmental disorders.
TEST-4626 MVK Gene Porokeratosis Type 3, Disseminated Superficial Actinic Genetic Test This genetic test evaluates the MVK gene for mutations associated with Disseminated Superficial Actinic Porokeratosis (DSAP). It identifies pathogenic variants to aid in diagnosis...	Peripheral whole blood (EDTA), genomic 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 ["MVK gene mutations", "Copy Number Variants (CNVs) in MVK gene"] Parameters [] Preparation ["No fasting required.", "Inform the team of all medications and supplements before collection."] Indications ["Diagnosis of Disseminated Superficial Actinic Porokeratosis (DSAP)", "Family risk assessment for DSAP", "Personalized management of DSAP", "Differentiation from other porokeratosis variants"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: L56.5, Z13.79, Z84.8 Clinical summary This genetic test evaluates the MVK gene for mutations associated with Disseminated Superficial Actinic Porokeratosis (DSAP). It identifies pathogenic variants to aid in diagnosis and risk assessment.
TEST-2676 MYO18B Gene Sequencing for Klippel‑Feil Syndrome Type 4 (Autosomal Dominant with Myopathy and Facial Dysmorphism) Test This test detects pathogenic variants in the MYO18B gene associated with Klippel‑Feil syndrome type 4, characterized by cervical spine fusion, myopathy, and facial dysmorphism.	Peripheral whole blood (EDTA) 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 ["Pathogenic variants in MYO18B gene", "Single-nucleotide variants", "Small indels"] Parameters [] Preparation ["No fasting required", "No medication withholding required"] Indications ["Clinical suspicion of Klippel‑Feil syndrome type 4", "Congenital cervical spine fusion", "Progressive myopathy", "Distinctive facial dysmorphism"] Measurement technique Confirm with laboratory Codes LOINC: 86283-0 ICD-10: Q76.1 Clinical summary This test detects pathogenic variants in the MYO18B gene associated with Klippel‑Feil syndrome type 4, characterized by cervical spine fusion, myopathy, and facial dysmorphism.
TEST-5032 NDUFAF5 Gene Mitochondrial Complex I Deficiency Genetic Test This test identifies pathogenic DNA variants in the NDUFAF5 gene, which are responsible for mitochondrial complex I deficiency.	Peripheral whole blood, extracted DNA, or dried blood spot (FTA card)	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 NDUFAF5 gene", "Copy Number Variants (CNV) in the NDUFAF5 gene"] Parameters [] Preparation ["No special dietary preparation is needed", "Mandatory pre-test genetic counselling session required"] Indications ["Clinical suspicion of mitochondrial complex I deficiency", "Diagnosis of Leigh syndrome", "Diagnosis of progressive encephalopathy", "Diagnosis of cardiomyopathy"] Measurement technique Confirm with laboratory Codes LOINC: 51966-7 ICD-10: E88.49, G31.89 Clinical summary This test identifies pathogenic DNA variants in the NDUFAF5 gene, which are responsible for mitochondrial complex I deficiency.

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.