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 2776–2789 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-2743 ZIC2 Gene Holoprosencephaly Type 5 Genetic Test This diagnostic test evaluates the ZIC2 gene for pathogenic variants associated with holoprosencephaly type 5.	Whole Blood (EDTA), DNA, 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 ZIC2 gene"] Parameters [] Preparation [] Indications ["Suspected holoprosencephaly type 5", "Genetic confirmation of ZIC2-related disorder"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q04.2 Clinical summary This diagnostic test evaluates the ZIC2 gene for pathogenic variants associated with holoprosencephaly type 5.
TEST-2793 ZIC3 Gene Heterotaxy Visceral Type 1 Genetic Test This test identifies pathogenic variants in the ZIC3 gene associated with visceral heterotaxy type 1.	Peripheral Whole Blood (EDTA), FTA Card, or Extracted Genomic 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 ZIC3 gene", "Single nucleotide variants (SNVs)", "Insertions and deletions (indels)", "Copy number variants (CNVs)"] Parameters [] Preparation ["No specific patient preparation required"] Indications ["Diagnosis of visceral heterotaxy type 1", "Risk stratification", "Informed reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 81265-5 ICD-10: Q89.3 Clinical summary This test identifies pathogenic variants in the ZIC3 gene associated with visceral heterotaxy type 1.
TEST-2163 ZIC5 Gene Sequencing Test (NGS) for Brain Disorders This test identifies pathogenic variants in the ZIC5 gene associated with congenital brain malformations and developmental delays.	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 ZIC5 gene"] Parameters [] Preparation ["No fasting required", "Mandatory pre-test genetic counselling session"] Indications ["Congenital brain malformations", "Developmental delays", "Dysmorphic features"] Measurement technique Confirm with laboratory Codes LOINC: 51966-2 ICD-10: Q04.8 Clinical summary This test identifies pathogenic variants in the ZIC5 gene associated with congenital brain malformations and developmental delays.
TEST-4814 ZMPSTE24 Gene Genetic Test for Mandibuloacral Dysplasia with Type B Lipodystrophy This test evaluates the ZMPSTE24 gene for pathogenic variants associated with mandibuloacral dysplasia with type B lipodystrophy.	Peripheral Whole Blood (3–5 mL in EDTA tube) or FTA Card 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 ZMPSTE24 gene", "Coding region and splice sites of ZMPSTE24"] Parameters [] Preparation ["Formal genetic counselling session with pedigree analysis required", "Written informed consent required"] Indications ["Suspected mandibuloacral dysplasia with type B lipodystrophy", "Genetic counselling for affected families"] Measurement technique Confirm with laboratory Codes LOINC: 94086-4 ICD-10: Q87.1 Clinical summary This test evaluates the ZMPSTE24 gene for pathogenic variants associated with mandibuloacral dysplasia with type B lipodystrophy.
TEST-4608 ZMPSTE24 Gene Sequencing for Lethal Restrictive Dermopathy Test This test evaluates the ZMPSTE24 gene for pathogenic variants associated with lethal restrictive dermopathy.	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 ZMPSTE24 gene"] Parameters [] Preparation [] Indications ["Diagnosis of suspected lethal restrictive dermopathy", "Carrier screening for ZMPSTE24 mutations", "Prenatal planning"] Measurement technique Confirm with laboratory Codes LOINC: 21665-7 ICD-10: Q80.8 Clinical summary This test evaluates the ZMPSTE24 gene for pathogenic variants associated with lethal restrictive dermopathy.
TEST-5434 ZNF311 Gene Neurodevelopmental Disorder Genetic Test This test evaluates the ZNF311 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 ["Pathogenic variants in the ZNF311 gene", "Single nucleotide variants (SNVs)", "Insertions/deletions (indels)", "Copy number variations (CNVs)"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any recent blood transfusions or bone marrow transplants"] Indications ["Suspected ZNF311-related neurodevelopmental disorder", "Confirmation of diagnosis", "Guiding early interventions", "Family history of ZNF311-related conditions"] Measurement technique Confirm with laboratory Codes LOINC: 81268-7 ICD-10: F84.0, F70–F79 Clinical summary This test evaluates the ZNF311 gene for pathogenic variants associated with neurodevelopmental disorders.
TEST-4944 ZNF41 Gene Mental Retardation, X-linked Type 89 Genetic Test This test analyzes the ZNF41 gene to identify pathogenic variants associated with X-linked intellectual disability type 89.	Peripheral Whole Blood (3-5 mL EDTA tube) or FTA Card 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 ZNF41 gene", "Coding regions and splice sites of ZNF41"] Parameters [] Preparation ["Do not discontinue prescribed antiepileptic, neuroleptic, or behavioral medication unless directed by a physician."] Indications ["Diagnosis of X-linked intellectual disability type 89 (XLID89)", "Family history of XLID89", "Genetic counseling for recurrence risk"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: F79 Clinical summary This test analyzes the ZNF41 gene to identify pathogenic variants associated with X-linked intellectual disability type 89.
TEST-3527 ZNF469 Gene Brittle Cornea Syndrome Genetic Test This test evaluates the ZNF469 gene for pathogenic variants associated with Brittle Cornea Syndrome.	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 ["ZNF469 gene coding regions", "ZNF469 gene splice sites"] Parameters [] Preparation [] Indications ["Diagnosis of Brittle Cornea Syndrome", "Identification of carriers in families with a history of the condition", "Genetic counseling for connective tissue disorders"] Measurement technique Confirm with laboratory Codes LOINC: 98544-9 ICD-10: Q78.8 Clinical summary This test evaluates the ZNF469 gene for pathogenic variants associated with Brittle Cornea Syndrome.
TEST-5055 ZNF674 Gene Mental Retardation, X-Linked Type 92 Genetic Test This test identifies pathogenic variants in the ZNF674 gene associated with X-linked intellectual disability type 92.	Whole Blood (peripheral venous or capillary 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 ["ZNF674 gene sequence", "Single-nucleotide variants", "Small insertions and deletions", "Copy number variants"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any recent blood transfusions"] Indications ["Suspected X-linked intellectual disability type 92", "Family history of X-linked intellectual disability", "Genetic counselling for developmental delay"] Measurement technique Confirm with laboratory Codes LOINC: 86246-4 ICD-10: F79, Q99.8, Z14.8 Clinical summary This test identifies pathogenic variants in the ZNF674 gene associated with X-linked intellectual disability type 92.
TEST-3949 ZNF778 Gene-Associated Autism: Genetic Test This test identifies pathogenic variants in the ZNF778 gene associated with autism spectrum disorder.	Peripheral whole blood 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 ZNF778 gene"] Parameters [] Preparation [] Indications ["Suspected ZNF778-related autism", "Genetic counseling for families with autism spectrum disorder"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: F84.0 Clinical summary This test identifies pathogenic variants in the ZNF778 gene associated with autism spectrum disorder.
TEST-1915 ZNF783 Gene Prostate Cancer Genetic Test This test evaluates for mutations in the ZNF783 gene, which are associated with an increased risk of developing prostate cancer.	Peripheral Whole Blood	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ZNF783 gene mutations", "Inherited genetic variants"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of all medications"] Indications ["Prostate cancer risk assessment", "Prognostication", "Guiding precision therapy"] Measurement technique Confirm with laboratory Codes LOINC: 101262-9 ICD-10: Z13.85 Clinical summary This test evaluates for mutations in the ZNF783 gene, which are associated with an increased risk of developing prostate cancer.
TEST-5039 ZNF81 Gene X-Linked Intellectual Disability Type 45 Genetic Test This genetic test identifies mutations in the ZNF81 gene associated with X-linked intellectual disability type 45.	Peripheral whole blood or saliva sample	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 ZNF81 gene", "Coding exons and splice sites of the ZNF81 gene"] Parameters [{"name": "Diagnostic Sensitivity", "reference_range": "99.9%"}, {"name": "Targeted Coverage", "reference_range": ">1000x"}] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Individuals with suspected X-linked intellectual disability type 45", "Family history of X-linked intellectual disability type 45", "Neurodevelopmental disorders with unclear etiology"] Measurement technique Confirm with laboratory Codes LOINC: 94291-7 ICD-10: F78.8 Clinical summary This genetic test identifies mutations in the ZNF81 gene associated with X-linked intellectual disability type 45.
TEST-3433 ZP1 Gene Oocyte Maturation Defect Genetic Test This genetic test identifies pathogenic mutations within the ZP1 gene associated with oocyte maturation arrest and female infertility.	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 ["Pathogenic variants in the ZP1 gene coding region", "Splice site variants"] Parameters [] Preparation ["No special preparation required", "Fasting is not required", "Provide detailed clinical history and family pedigree chart"] Indications ["Women with unexplained infertility", "Recurrent IVF failure", "Primary ovarian insufficiency", "Suspected oocyte maturation arrest based on poor embryo development or empty follicle syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 94086-1 ICD-10: N97.8 Clinical summary This genetic test identifies pathogenic mutations within the ZP1 gene associated with oocyte maturation arrest and female infertility.
TEST-3133 ZSWIM6 Gene Acromelic Frontonasal Dysostosis Genetic Test This test identifies pathogenic variants in the ZSWIM6 gene associated with acromelic frontonasal dysostosis.	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 ZSWIM6 gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any relevant medications"] Indications ["Suspected acromelic frontonasal dysostosis", "Differential diagnosis of craniofacial syndromes"] Measurement technique Confirm with laboratory Codes LOINC: 81397-3 ICD-10: Q87.0 Clinical summary This test identifies pathogenic variants in the ZSWIM6 gene associated with acromelic frontonasal dysostosis.

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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