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

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Genetic test prices

Showing 796–805 of 805 matching tests.

Genetic diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4461 XPC Gene (Xeroderma Pigmentosum Group C) Genetic Test This genetic test analyzes the XPC gene for pathogenic variants associated with Xeroderma Pigmentosum Group C, a disorder causing extreme UV sensitivity and increased skin cancer r...	Whole Blood, 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 XPC gene"] Parameters [] Preparation ["No fasting or medication withdrawal is required", "Mandatory pre-test genetic counseling session"] Indications ["Suspected Xeroderma Pigmentosum Group C", "Family history of Xeroderma Pigmentosum", "Extreme photosensitivity"] Measurement technique Confirm with laboratory Codes LOINC: 94233-5 ICD-10: Q82.1 Clinical summary This genetic test analyzes the XPC gene for pathogenic variants associated with Xeroderma Pigmentosum Group C, a disorder causing extreme UV sensitivity and increased skin cancer risk.
TEST-2334 XRCC4 Gene Genetic Test (Short Stature, Microcephaly, Endocrine Dysfunction) This test evaluates the XRCC4 gene for pathogenic mutations linked to specific developmental and endocrine conditions.	Peripheral whole blood or extracted DNA	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["XRCC4 gene sequence", "Pathogenic variants in XRCC4"] Parameters [] Preparation ["Mandatory pre-test genetic counseling session", "Documentation of family history (pedigree)", "Obtain informed consent"] Indications ["Unexplained growth failure", "Microcephaly", "Hormonal abnormalities", "Family history suggesting XRCC4-related disorder"] Measurement technique Confirm with laboratory Codes LOINC: 81321-7 ICD-10: Q02, R62.52 Clinical summary This test evaluates the XRCC4 gene for pathogenic mutations linked to specific developmental and endocrine conditions.
TEST-3576 YAP1 Gene Coloboma, Ocular, with or without Hearing Impairment, Cleft Lip/Palate, and/or Mental Retardation Genetic Test This test evaluates the YAP1 gene for pathogenic variants associated with coloboma-related syndromes.	Whole Blood (Peripheral)	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 YAP1 gene", "Single nucleotide variants (SNVs)", "Insertions/deletions (indels)", "Copy number variants (CNVs)"] Parameters [] Preparation ["A detailed clinical history focusing on ocular, auditory, craniofacial, and developmental milestones is mandatory.", "A genetic counseling session is required to construct a pedigree chart.", "Informed consent must be documented."] Indications ["Individuals with clinical features suggestive of YAP1-related disorders", "Family history of YAP1-related conditions", "Prenatal diagnosis in high-risk pregnancies"] Measurement technique Confirm with laboratory Codes LOINC: 82382-9 ICD-10: Q12.2, Q13.0, Q14.8 Clinical summary This test evaluates the YAP1 gene for pathogenic variants associated with coloboma-related syndromes.
TEST-2300 ZBTB16 Gene Sequencing (NGS) Test This diagnostic test evaluates the ZBTB16 gene for pathogenic variants associated with skeletal defects, genital hypoplasia, and intellectual disability.	Peripheral 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 variants in the ZBTB16 gene"] Parameters [{"name": "Diagnostic Sensitivity", "reference_range": "99.9%"}] Preparation ["No special preparation is needed", "Genetic counselling session recommended prior to testing"] Indications ["Individuals presenting with clinical features suggestive of ZBTB16-related disorders", "Family history of ZBTB16-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 38075-4 ICD-10: Z13.79 Clinical summary This diagnostic test evaluates the ZBTB16 gene for pathogenic variants associated with skeletal defects, genital hypoplasia, and intellectual disability.
TEST-5962 ZC4H2 Gene Wieacker‑Wolff Syndrome Genetic Test This test identifies mutations in the ZC4H2 gene associated with Wieacker-Wolff syndrome.	Whole Blood (Peripheral), FTA Card Dried Blood Spot, or Extracted Genomic DNA	3 – 4 weeks (expedited available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ZC4H2 gene", "Coding and splice-site variants"] Parameters [] Preparation ["No fasting required", "No medication changes required"] Indications ["Suspected Wieacker-Wolff syndrome", "Family history of Wieacker-Wolff syndrome", "X-linked neurodevelopmental disorder investigation"] Measurement technique Confirm with laboratory Codes LOINC: 79255-8 ICD-10: Q87.8 Clinical summary This test identifies mutations in the ZC4H2 gene associated with Wieacker-Wolff syndrome.
TEST-2756 ZEB2 Gene Hirschsprung Disease Genetic Test This test evaluates the ZEB2 gene for pathogenic variants associated with Hirschsprung disease and Mowat-Wilson syndrome.	Whole Blood (EDTA), Extracted DNA, Dried Blood 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 ZEB2 gene", "Point mutations", "Small insertions and deletions", "Copy number variants"] Parameters [] Preparation [] Indications ["Paediatric patients with symptoms of Hirschsprung disease", "Neonates with delayed passage of meconium (>48 hours)", "Individuals with a family history of ZEB2-related syndromes"] Measurement technique Confirm with laboratory Codes LOINC: 44397-5 ICD-10: Q43.1 Clinical summary This test evaluates the ZEB2 gene for pathogenic variants associated with Hirschsprung disease and Mowat-Wilson syndrome.
TEST-4213 ZFPM2 Gene Diaphragmatic Hernia Type 3 Genetic Test This test identifies pathogenic variants in the ZFPM2 gene associated with congenital diaphragmatic hernia (CDH) type 3.	Peripheral whole blood (EDTA), buccal swab, 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 ZFPM2 gene"] Parameters [] Preparation ["No specific fasting required", "No medication adjustments needed"] Indications ["Confirmation of genetic cause for CDH type 3", "Family history of CDH type 3", "Recurrence risk assessment", "Prenatal planning"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: Q79.0 Clinical summary This test identifies pathogenic variants in the ZFPM2 gene associated with congenital diaphragmatic hernia (CDH) type 3.
TEST-5708 ZFR Gene SPG71 Genetic Test This test identifies pathogenic variants in the ZFR gene associated with Hereditary Spastic Paraplegia type 71 (SPG71).	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 ZFR gene", "Single nucleotide variants", "Small insertions/deletions"] Parameters [] Preparation ["Mandatory genetic counseling session required", "Inform phlebotomist if taking anticoagulants", "No fasting necessary"] Indications ["Diagnosis of Hereditary Spastic Paraplegia type 71 (SPG71)", "Family planning for individuals with a family history of SPG71", "Prognosis and targeted therapy guidance for SPG71 patients"] Measurement technique Confirm with laboratory Codes LOINC: 98430-2 ICD-10: G11.4, Z13.79, Z15.89 Clinical summary This test identifies pathogenic variants in the ZFR gene associated with Hereditary Spastic Paraplegia type 71 (SPG71).
TEST-3660 ZNF423 Gene Nephronophthisis Type 14 Genetic Test This test evaluates the ZNF423 gene for pathogenic variants associated with Nephronophthisis Type 14, a rare genetic kidney disorder.	Peripheral blood (EDTA) 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 ZNF423 gene", "Single nucleotide variants", "Small insertions and deletions", "Copy number variations"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications without consulting your physician"] Indications ["Diagnosis of Nephronophthisis Type 14", "Genetic predisposition assessment for kidney disease", "Family planning and cascade screening"] Measurement technique Confirm with laboratory Codes LOINC: 81201-3 ICD-10: Q61.5 Clinical summary This test evaluates the ZNF423 gene for pathogenic variants associated with Nephronophthisis Type 14, a rare genetic kidney disorder.
TEST-4961 ZNF711 Gene Genetic Test (X-Linked Intellectual Disability Type 97) This test analyzes the ZNF711 gene for mutations associated with X-linked intellectual disability type 97.	Peripheral whole blood, extracted DNA, or 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 ["ZNF711 gene coding region", "Deletion/duplication analysis of ZNF711 gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Suspected X-linked intellectual disability type 97", "Family history of XLID97", "Evaluation of developmental delay and intellectual disability"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q87.8 Clinical summary This test analyzes the ZNF711 gene for mutations associated with X-linked intellectual disability type 97.

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.

Before booking

Use the test details as a conversation starter

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.