Diagnostic options · UAE

Genetic tests in Dubai & UAE

Compare available Genetic 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

805

Listed price range

600.00–30,000.00 AED

Clinical preparation

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Genetic test prices

Showing 211–225 of 805 matching tests.

Genetic diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-1636 DMD/BMD Mutation Screening (26 Exons) Test This test screens for common deletions and duplications within the 26 exons of the DMD gene, associated with Duchenne and Becker muscular dystrophies.	Amniotic fluid or chorionic villus sampling	4–5 business days	1,400.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Deletions in DMD gene exons", "Duplications in DMD gene exons"] Parameters [] Preparation [] Indications ["Family history of DMD/BMD", "Known maternal carrier status", "Clinical suspicion during pregnancy"] Measurement technique Confirm with laboratory Codes LOINC: 87762-1 ICD-10: G71.0 Clinical summary This test screens for common deletions and duplications within the 26 exons of the DMD gene, associated with Duchenne and Becker muscular dystrophies.
TEST-6346 DMGDH Gene (Dimethylglycine Dehydrogenase Deficiency) Genetic Test This genetic test identifies pathogenic variants in the DMGDH gene associated with dimethylglycine dehydrogenase deficiency.	Whole blood (EDTA), DNA FTA Card, or Extracted DNA (peripheral 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 DMGDH gene"] Parameters [] Preparation ["Fasting is not required", "Provide whole blood, DNA FTA card, or extracted DNA"] Indications ["Suspected dimethylglycine dehydrogenase deficiency", "Family history of the disorder", "Genetic counselling for at-risk relatives"] Measurement technique Confirm with laboratory Codes LOINC: 94558-4 ICD-10: E72.8, E72.9 Clinical summary This genetic test identifies pathogenic variants in the DMGDH gene associated with dimethylglycine dehydrogenase deficiency.
TEST-5028 DMP1 Gene Autosomal Recessive Hypophosphatemic Rickets Type 1 (ARHR1) Genetic Test This test evaluates the DMP1 gene for mutations associated with Autosomal Recessive Hypophosphatemic Rickets Type 1 (ARHR1).	Whole Blood (EDTA) or 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 ["DMP1 gene sequence", "Pathogenic variants in DMP1"] Parameters [] Preparation ["Pre-test genetic counselling session recommended", "Inform lab about recent blood transfusions"] Indications ["Suspected Autosomal Recessive Hypophosphatemic Rickets Type 1 (ARHR1)", "Family history of ARHR1", "Evaluation of hypophosphatemia with skeletal abnormalities"] Measurement technique Confirm with laboratory Codes LOINC: 79692-0 ICD-10: E83.31, Z13.79, Z82.79 Clinical summary This test evaluates the DMP1 gene for mutations associated with Autosomal Recessive Hypophosphatemic Rickets Type 1 (ARHR1).
TEST-5481 DNAH9 Gene Primary Ciliary Dyskinesia Genetic Test (NGS) This test evaluates the DNAH9 gene for mutations associated with primary ciliary dyskinesia (PCD). It identifies variations, including copy number changes and deep intronic variant...	Peripheral Whole Blood, Extracted DNA, or Buccal Swab	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DNAH9 gene sequence", "Copy Number Variations (CNVs) in DNAH9", "Deep intronic variants in DNAH9"] Parameters [] Preparation ["Provide detailed clinical history", "Three-generation pedigree recommended"] Indications ["Suspected primary ciliary dyskinesia", "Chronic respiratory infections", "Situs inversus", "Infertility"] Measurement technique Confirm with laboratory Codes LOINC: 81247-7 ICD-10: Q34.8, Z15.89, Z14.8 Clinical summary This test evaluates the DNAH9 gene for mutations associated with primary ciliary dyskinesia (PCD). It identifies variations, including copy number changes and deep intronic variants, using Next Generation Sequencing.
TEST-4284 DNAJC19 Gene Dilated Cardiomyopathy with Ataxia Genetic Test This genetic test evaluates the DNAJC19 gene for variants associated with dilated cardiomyopathy and cerebellar ataxia.	Peripheral Whole Blood (EDTA tube)	10–14 working days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DNAJC19 gene variants", "Pathogenic and likely pathogenic variants"] Parameters [] Preparation [] Indications ["Suspected 3-methylglutaconic aciduria type V", "Family history suggestive of 3-methylglutaconic aciduria type V"] Measurement technique Confirm with laboratory Codes LOINC: 94224-6 ICD-10: I42.0, G11.1 Clinical summary This genetic test evaluates the DNAJC19 gene for variants associated with dilated cardiomyopathy and cerebellar ataxia.
TEST-3950 DNM2 Gene Centronuclear Myopathy Type 1 Genetic Test This genetic test identifies pathogenic variants in the DNM2 gene associated with centronuclear myopathy type 1.	Peripheral whole blood or 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 ["DNM2 gene sequence", "Pathogenic variants"] Parameters [] Preparation [] Indications ["Clinical features suggestive of congenital myopathy", "Muscle biopsy showing central nuclei", "Family members of diagnosed individuals"] Measurement technique Confirm with laboratory Codes LOINC: 81307-5 ICD-10: G71.2 Clinical summary This genetic test identifies pathogenic variants in the DNM2 gene associated with centronuclear myopathy type 1.
TEST-3966 DNMT1 Gene Autosomal Recessive Cerebellar Ataxia with Deafness and Narcolepsy Genetic Test This test identifies pathogenic variants in the DNMT1 gene associated with autosomal recessive cerebellar ataxia, deafness, and narcolepsy.	Peripheral whole blood (EDTA), saliva (Oragene), or extracted DNA	3–4 Weeks (Rapid option available upon request)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the DNMT1 gene", "Full coding region of the DNMT1 gene (exons and splice sites)"] Parameters [] Preparation ["No fasting required", "No special diet required", "No medication adjustments needed unless instructed by your doctor"] Indications ["Individuals presenting with clinical features of cerebellar ataxia, deafness, and narcolepsy", "Family history of autosomal recessive neurogenetic disorders", "Diagnostic confirmation for clinical management and genetic counselling"] Measurement technique Confirm with laboratory Codes LOINC: 81226-8 ICD-10: G11.8, H90.3, Z13.79 Clinical summary This test identifies pathogenic variants in the DNMT1 gene associated with autosomal recessive cerebellar ataxia, deafness, and narcolepsy.
TEST-5211 DOK7 Gene Myasthenic Syndrome, Congenital, Type 10 Genetic Test This genetic test evaluates the DOK7 gene for pathogenic variants associated with Congenital Myasthenic Syndrome Type 10 (CMS10).	Whole Blood (4 mL) 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 DOK7 gene", "Point mutations", "Small indels", "Copy number changes"] Parameters [] Preparation ["No fasting required", "No medication adjustment required unless directed by physician"] Indications ["Individuals with symptoms suggesting congenital myasthenic syndrome", "Asymptomatic family members seeking carrier status", "Reproductive planning when one parent carries a DOK7 mutation"] Measurement technique Confirm with laboratory Codes LOINC: 81431-6 ICD-10: G70.2 Clinical summary This genetic test evaluates the DOK7 gene for pathogenic variants associated with Congenital Myasthenic Syndrome Type 10 (CMS10).
TEST-6246 DPYS Gene Dihydropyrimidinuria Genetic Test This genetic test detects pathogenic variants in the DPYS gene associated with dihydropyrimidinuria.	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 ["Pathogenic variants in the DPYS gene", "Single nucleotide variants", "Small insertions/deletions", "Copy number changes"] Parameters [] Preparation [] Indications ["Diagnosis of dihydropyrimidinuria", "Family screening for DPYS gene variants", "Personalized management of suspected metabolic disorders"] Measurement technique Confirm with laboratory Codes LOINC: 21639-8 ICD-10: E79.8 Clinical summary This genetic test detects pathogenic variants in the DPYS gene associated with dihydropyrimidinuria.
TEST-3871 DRD5 Gene ADHD Genetic Test This test analyzes the DRD5 gene for variants associated with ADHD susceptibility and treatment response using Next Generation Sequencing.	Peripheral Whole Blood (Venipuncture or Finger-prick)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DRD5 gene variants", "Single nucleotide variants", "Small insertions/deletions"] Parameters [{"name": "Diagnostic Sensitivity", "reference_range": "99.9%"}] Preparation [] Indications ["Suspected ADHD", "Personalized medication selection", "Familial risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 21638-5 ICD-10: F90.9 Clinical summary This test analyzes the DRD5 gene for variants associated with ADHD susceptibility and treatment response using Next Generation Sequencing.
TEST-4552 DSP Gene (Skin Fragility-Woolly Hair Syndrome) Genetic Test This test evaluates the entire DSP gene for mutations associated with skin fragility-woolly hair syndrome and related cardiomyopathy.	Whole Blood / DNA (Peripheral Venipuncture or FTA Card)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DSP gene sequence", "Mutations (SNVs, indels, CNVs)"] Parameters [] Preparation ["No specific fasting required", "Inform lab of recent blood transfusion or bone marrow transplant"] Indications ["Suspected skin fragility-woolly hair syndrome", "Family history of the condition", "Unexplained cardiomyopathy"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q84.2, Q82.8 Clinical summary This test evaluates the entire DSP gene for mutations associated with skin fragility-woolly hair syndrome and related cardiomyopathy.
TEST-4838 DSP Gene Keratosis Palmoplantaris Striata Type 2 Genetic Test This genetic test analyzes the DSP gene to detect mutations associated with Keratosis Palmoplantaris Striata Type 2.	Whole Blood, DNA FTA Card, Extracted DNA	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DSP gene mutations (SNVs, indels, CNVs)", "Analytical sensitivity"] Parameters [] Preparation [] Indications ["Suspected diagnosis of Keratosis Palmoplantaris Striata Type 2", "Family history of hereditary skin conditions"] Measurement technique Confirm with laboratory Codes LOINC: 79691-4 ICD-10: Q82.8, Z15.89, Z84.81 Clinical summary This genetic test analyzes the DSP gene to detect mutations associated with Keratosis Palmoplantaris Striata Type 2.
TEST-4240 DSP Gene NGS Test for Dilated Cardiomyopathy, Woolly Hair, Keratoderma & Tooth Agenesis This diagnostic test evaluates the entire coding region of the DSP gene for pathogenic variants associated with Carvajal syndrome.	Peripheral 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 DSP gene", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)", "Copy Number Variants (CNVs)"] Parameters [] Preparation ["No fasting required", "Provide details of family cardiac events", "Provide names of affected relatives"] Indications ["Diagnosis of Carvajal syndrome", "Family screening for DSP gene variants", "Pre-implantation genetic diagnosis (PGD)", "Cascade testing for at-risk relatives"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: I42.0, Q84.2, L85.2 Clinical summary This diagnostic test evaluates the entire coding region of the DSP gene for pathogenic variants associated with Carvajal syndrome.
TEST-5261 DSPP Gene Dentin Dysplasia Type 2 Genetic Test This test analyzes the DSPP gene for pathogenic variants associated with hereditary dentin disorders like Dentin Dysplasia Type 2 and Dentinogenesis Imperfecta.	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 ["DSPP gene sequence", "Point mutations", "Small insertions/deletions", "Copy number variations"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting your physician"] Indications ["Suspected Dentin Dysplasia Type 2", "Suspected Dentinogenesis Imperfecta", "Family history of hereditary dentin disorders", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 81335-2 ICD-10: K00.5 Clinical summary This test analyzes the DSPP gene for pathogenic variants associated with hereditary dentin disorders like Dentin Dysplasia Type 2 and Dentinogenesis Imperfecta.
TEST-5220 DSPP Gene Dentinogenesis Imperfecta Shields Type 2 Genetic Test This genetic test identifies pathogenic variants in the DSPP gene, confirming a diagnosis of dentinogenesis imperfecta Shields type 2.	Whole Blood (EDTA), Extracted DNA, or FTA Card Blood Spot	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 DSPP gene", "Copy-number variations in the DSPP gene"] Parameters [] Preparation [] Indications ["Suspected diagnosis of dentinogenesis imperfecta Shields type 2", "Differentiation from other dental genetic disorders", "Family risk assessment", "Tailored treatment planning"] Measurement technique Confirm with laboratory Codes LOINC: 93382-9 ICD-10: K00.5, Z13.71, Z15.89 Clinical summary This genetic test identifies pathogenic variants in the DSPP gene, confirming a diagnosis of dentinogenesis imperfecta Shields type 2.

Category overview

Genetic: overview

Unlocking the blueprint of your DNA provides profound, proactive insights into your family’s future and personal health risks. Integrated within our advanced Biochemistry and molecular services, specialized Genetic testing evaluates inherited traits, metabolic predispositions, and carrier statuses. Utilizing cutting-edge diagnostic technology, comprehensive genetic screening offers the vital clarity needed to safely guide tailored medical strategies and family planning. As an undisputed leader in innovation among diagnostic labs in Dubai and the UAE, DNA Labs guarantees the highest standards of strict patient confidentiality, unparalleled diagnostic precision, and rapid reporting. Empower your health decisions with certainty—book your genetic testing in UAE, coordinate a secure sample collection, or connect with our specialized genetics team today.

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