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 2716–2730 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3514 WDR19 Gene Senior‑Loken Syndrome Type 8 Genetic Test This test analyzes the WDR19 gene for mutations associated with Senior-Loken syndrome type 8.	Peripheral Whole Blood or Extracted DNA	10–14 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["WDR19 gene coding region variants (SNVs, indels)"] Parameters [] Preparation [] Indications ["Suspected Senior-Loken syndrome type 8", "Family history of Senior-Loken syndrome type 8", "Clinical presentation consistent with ciliopathy"] Measurement technique Confirm with laboratory Codes LOINC: 94252-3 ICD-10: Q87.89, Q61.4 Clinical summary This test analyzes the WDR19 gene for mutations associated with Senior-Loken syndrome type 8.
TEST-2316 WDR19 Gene Sequencing (Short-Rib Thoracic Dysplasia Type 5) Genetic Test This test analyzes the WDR19 gene for mutations associated with short-rib thoracic dysplasia type 5 (SRTD5). It uses next-generation sequencing (NGS) to detect variants in coding e...	Peripheral 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 ["WDR19 gene coding exons", "WDR19 gene splice sites"] Parameters [] Preparation ["No special preparation required for the child"] Indications ["Clinical features of skeletal ciliopathy", "Suspicion of short-rib thoracic dysplasia type 5"] Measurement technique Confirm with laboratory Codes LOINC: 95308-5 ICD-10: Q77.2 Clinical summary This test analyzes the WDR19 gene for mutations associated with short-rib thoracic dysplasia type 5 (SRTD5). It uses next-generation sequencing (NGS) to detect variants in coding exons and splice sites.
TEST-5866 WDR27 Gene Sequencing for Brain Disorders (Genetic Test) This test analyzes the entire WDR27 gene to identify pathogenic variants associated with hereditary neurological disorders.	Whole 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 WDR27 gene", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["Fasting is not required", "Sample can be collected at any time"] Indications ["Confirmation of genetic diagnosis for hereditary brain disorders", "Guiding treatment planning", "Family counseling", "Carrier detection"] Measurement technique Confirm with laboratory Codes LOINC: 81322-1 ICD-10: G11.8, Q04.8 Clinical summary This test analyzes the entire WDR27 gene to identify pathogenic variants associated with hereditary neurological disorders.
TEST-2328 WDR34 Gene Sequencing (Short-Rib Thoracic Dysplasia Type 11 ± Polydactyly) Genetic Test This test evaluates the WDR34 gene for mutations associated with Short-Rib Thoracic Dysplasia Type 11 (SRTD11), a rare genetic disorder affecting skeletal development.	Whole Blood (EDTA), Extracted DNA, or Dried Blood Spot (FTA Card)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["WDR34 gene mutations", "Single nucleotide variants", "Insertions", "Deletions"] Parameters [] Preparation ["Do not discontinue prescribed medication without consulting your physician", "Inform the collection team if on anticoagulants", "Inform the collection team if received a blood transfusion within the past two weeks"] Indications ["Pediatric diagnosis of SRTD11", "Prenatal diagnosis of SRTD11", "Carrier screening for SRTD11", "Familial variant analysis"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q77.2, Q69.9 Clinical summary This test evaluates the WDR34 gene for mutations associated with Short-Rib Thoracic Dysplasia Type 11 (SRTD11), a rare genetic disorder affecting skeletal development.
TEST-2928 WDR35 Gene (Cranioectodermal Dysplasia Type 2) Genetic Test This genetic test identifies pathogenic variants in the WDR35 gene associated with Cranioectodermal Dysplasia Type 2.	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 WDR35 gene", "Deletion/duplication analysis of the WDR35 gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab if currently receiving heparin therapy"] Indications ["Suspected Cranioectodermal Dysplasia Type 2", "Family history of CED2", "Genetic counseling for recurrence risk"] Measurement technique Confirm with laboratory Codes LOINC: 90369-8 ICD-10: Q87.8 Clinical summary This genetic test identifies pathogenic variants in the WDR35 gene associated with Cranioectodermal Dysplasia Type 2.
TEST-2312 WDR35 Gene Short-Rib Thoracic Dysplasia Type 7 With or Without Polydactyly Genetic Test This genetic test analyzes the WDR35 gene to identify mutations associated with short-rib thoracic dysplasia type 7.	Whole Blood (EDTA), 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 ["WDR35 gene coding region", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["No fasting required", "No medication washout required"] Indications ["Clinical suspicion of short-rib thoracic dysplasia type 7", "Family history of skeletal dysplasia", "Need for definitive diagnosis for genetic counselling"] Measurement technique Confirm with laboratory Codes LOINC: 21665-5 ICD-10: Q77.2 Clinical summary This genetic test analyzes the WDR35 gene to identify mutations associated with short-rib thoracic dysplasia type 7.
TEST-3674 WDR36 Gene Glaucoma (Open Angle Type 1G) Genetic Test This test identifies mutations in the WDR36 gene associated with an increased risk of developing primary open-angle glaucoma type 1G.	Peripheral Whole Blood or Saliva	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["WDR36 gene mutations", "Genetic predisposition to primary open-angle glaucoma type 1G"] Parameters [] Preparation [] Indications ["Family history of early-onset open-angle glaucoma", "Diagnosis of open-angle glaucoma under 50 years of age"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: H40.10, Z13.5, Z15.89 Clinical summary This test identifies mutations in the WDR36 gene associated with an increased risk of developing primary open-angle glaucoma type 1G.
TEST-5404 WDR45 Gene Neurodegeneration with Brain Iron Accumulation Type 5 (BPAN) Genetic Test This test identifies pathogenic variants in the WDR45 gene associated with Beta-Propeller Protein-Associated Neurodegeneration (BPAN), also known as Neurodegeneration with Brain Ir...	Whole Blood (EDTA), Extracted DNA, FTA Card	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 WDR45 gene", "Single-Nucleotide Variants (SNVs)", "Indels", "Copy Number Variants (CNVs)"] Parameters [] Preparation ["No fasting required", "Mandatory genetic counselling session prior to collection"] Indications ["Suspicion of NBIA-spectrum disorder", "Developmental regression", "Movement disorders", "Characteristic brain MRI patterns"] Measurement technique Confirm with laboratory Codes LOINC: 82307-8 ICD-10: G23.0 Clinical summary This test identifies pathogenic variants in the WDR45 gene associated with Beta-Propeller Protein-Associated Neurodegeneration (BPAN), also known as Neurodegeneration with Brain Iron Accumulation Type 5 (NBIA5).
TEST-2297 WDR60 Gene Short‑Rib Thoracic Dysplasia Type 8 with or without Polydactyly Genetic Test This genetic test identifies pathogenic variants in the WDR60 gene associated with Short‑Rib Thoracic Dysplasia type 8 (SRTD8).	Whole Blood, Extracted DNA, 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 WDR60 gene", "Large deletions and duplications in the WDR60 gene"] Parameters [] Preparation ["Genetic counselling session mandatory before sample collection", "No specific fasting or medication restrictions mentioned"] Indications ["Newborns, infants, and children with clinical features suggestive of SRTD8", "Families with a history of SRTD8", "Unexplained neonatal deaths due to skeletal dysplasia", "Prenatal testing after prior genetic confirmation in the family"] Measurement technique Confirm with laboratory Codes LOINC: 59409-2 ICD-10: Q77.2 Clinical summary This genetic test identifies pathogenic variants in the WDR60 gene associated with Short‑Rib Thoracic Dysplasia type 8 (SRTD8).
TEST-2583 WDR62 Gene Microcephaly with Cortical Malformations, Autosomal Recessive Type 2 Genetic Test This test identifies pathogenic variants within the WDR62 gene associated with autosomal recessive primary microcephaly type 2 and cortical malformations.	Whole Blood, Extracted DNA, Dried Blood Spot (FTA Card)	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 WDR62 gene", "Single nucleotide variants", "Small indels"] Parameters [{"name": "Diagnostic Sensitivity", "reference_range": ">99.9% for single nucleotide variants and small indels within WDR62"}] Preparation ["Do not discontinue prescribed medications without consulting your treating physician.", "Inform phlebotomist of all current medications and supplements."] Indications ["Newborns and infants presenting with severe congenital microcephaly (head circumference < -3 SD)", "Cortical malformations on neuroimaging", "Family history suggesting recessive inheritance"] Measurement technique Confirm with laboratory Codes LOINC: 86709-3 ICD-10: Q02, Q04.8 Clinical summary This test identifies pathogenic variants within the WDR62 gene associated with autosomal recessive primary microcephaly type 2 and cortical malformations.
TEST-5439 WDR72 Gene Amelogenesis Imperfecta Type IIA3 (AI2A3) Genetic Test This genetic test identifies pathogenic variants in the WDR72 gene associated with Amelogenesis Imperfecta Type IIA3.	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 ["Pathogenic single nucleotide variants in WDR72 gene", "Small insertion/deletions in WDR72 gene"] Parameters [] Preparation ["Complete pre-genetic counselling session", "Provide a three-generation pedigree chart"] Indications ["Individuals with hypoplastic enamel", "Individuals with unusual tooth discoloration", "Individuals with a family history of hereditary dental anomalies and associated dermatological/skeletal signs"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: K00.5 Clinical summary This genetic test identifies pathogenic variants in the WDR72 gene associated with Amelogenesis Imperfecta Type IIA3.
TEST-2825 WDR73 Gene Galloway-Mowat Syndrome Genetic Test This test analyzes the WDR73 gene for pathogenic variants associated with Galloway-Mowat syndrome.	Whole blood (peripheral), 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 ["WDR73 gene variants", "Pathogenic mutations"] Parameters [] Preparation ["No fasting required", "Continue prescribed medications"] Indications ["Diagnosis of Galloway-Mowat syndrome", "Family planning", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 101426-0 ICD-10: Q87.8, Z13.71, Z14.8 Clinical summary This test analyzes the WDR73 gene for pathogenic variants associated with Galloway-Mowat syndrome.
TEST-4885 WDR81 Gene Analysis (CAMRQ2 Syndrome) Test This test detects pathogenic variants in the WDR81 gene associated with CAMRQ2 syndrome.	Whole Blood EDTA, Extracted DNA ≥ 1 µg, or FTA Card	21–28 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 WDR81 gene", "SNVs", "Indels", "Copy number variants (CNVs)", "Novel pathogenic variants"] Parameters [] Preparation ["No fasting required", "No medication discontinuation unless directed by physician"] Indications ["Symptomatic individuals requiring molecular confirmation", "Asymptomatic siblings for carrier screening", "Couples with a known family history seeking preconception genetic counselling"] Measurement technique Confirm with laboratory Codes LOINC: 81264-8 ICD-10: G11.1 Clinical summary This test detects pathogenic variants in the WDR81 gene associated with CAMRQ2 syndrome.
TEST-4016 WDR81 Gene Cerebellar Ataxia, Intellectual Disability, and Dysequilibrium Syndrome Type 2 (CAMRQ2) Genetic Test This genetic test identifies pathogenic variants within the WDR81 gene associated with Cerebellar Ataxia, Intellectual Disability, and Dysequilibrium Syndrome Type 2 (CAMRQ2).	Peripheral Whole Blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["WDR81 gene coding region variants", "Pathogenic mutations"] Parameters [] Preparation ["No fasting required", "Ensure patient is comfortable and well-hydrated"] Indications ["Suspected CAMRQ2 syndrome", "Family history of CAMRQ2", "Neurological symptoms consistent with CAMRQ2"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: G11.1, F70 Clinical summary This genetic test identifies pathogenic variants within the WDR81 gene associated with Cerebellar Ataxia, Intellectual Disability, and Dysequilibrium Syndrome Type 2 (CAMRQ2).
TEST-3534 WFS1 Gene (Cataract Type 41) Genetic Test This test evaluates the WFS1 gene for pathogenic variants associated with autosomal recessive cataracts type 41 and Wolfram syndrome.	Whole blood (EDTA tube) or FTA card (dried blood spot)	3–4 Weeks (expedited 2-week option available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variations (CNVs)", "WFS1 gene sequence"] Parameters [] Preparation ["No fasting required", "No medication changes required", "Mandatory pre-test genetic counselling session"] Indications ["Diagnosis of congenital/early-onset cataracts", "Diagnosis of Wolfram syndrome (DIDMOAD)", "Genetic counselling for families with a history of these conditions", "Carrier screening in at-risk individuals"] Measurement technique Confirm with laboratory Codes LOINC: 21662-0 ICD-10: Q12.0 Clinical summary This test evaluates the WFS1 gene for pathogenic variants associated with autosomal recessive cataracts type 41 and Wolfram syndrome.

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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