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 2401–2415 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4038 SOAT1 Gene Atherosclerosis Genetic Test This test evaluates the SOAT1 gene for variants associated with an increased risk of early-onset atherosclerosis.	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 ["SOAT1 gene variants", "Inherited risk for atherosclerosis"] Parameters [] Preparation [] Indications ["Assessment of inherited risk for early-onset atherosclerosis", "Personalized cardiovascular risk management"] Measurement technique Confirm with laboratory Codes LOINC: 21636-3 ICD-10: I70.90 Clinical summary This test evaluates the SOAT1 gene for variants associated with an increased risk of early-onset atherosclerosis.
TEST-4898 SOBP Gene Intellectual Disability, Anterior Maxillary Protrusion & Strabismus NGS Test This test identifies genetic variants in the SOBP gene associated with intellectual disability, anterior maxillary protrusion, and strabismus.	Whole blood (EDTA), extracted genomic DNA, dried FTA card	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 ["SOBP gene variants", "Single-nucleotide variants", "Small insertions/deletions", "Splicing variants"] Parameters [] Preparation ["No specific preparation required", "Provide a detailed three-generation family pedigree"] Indications ["Patients presenting with the syndromic triad of intellectual disability, anterior maxillary protrusion, and strabismus"] Measurement technique Confirm with laboratory Codes LOINC: 91606-7 ICD-10: F70.9, Q87.8 Clinical summary This test identifies genetic variants in the SOBP gene associated with intellectual disability, anterior maxillary protrusion, and strabismus.
TEST-3767 SOD1 Gene Amyotrophic Lateral Sclerosis Type 1 (ALS1) Genetic Test This genetic test evaluates the SOD1 gene for variants associated with Amyotrophic Lateral Sclerosis Type 1 (ALS1).	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 ["SOD1 gene variants (SNVs, indels)"] Parameters [{"name": "Analytical Sensitivity", "reference_range": ">99.9% for SNVs & small indels"}] Preparation ["No fasting required", "No medication changes required", "Mandatory pre-test genetic counselling session"] Indications ["Suspected familial ALS1", "Confirmation of clinical diagnosis", "Family member screening", "Clinical trial enrollment"] Measurement technique Confirm with laboratory Codes LOINC: 69548-9 ICD-10: G12.21, Z15.09, Z13.858 Clinical summary This genetic test evaluates the SOD1 gene for variants associated with Amyotrophic Lateral Sclerosis Type 1 (ALS1).
TEST-3551 SORD Gene Congenital Cataract Genetic Test This test evaluates the SORD gene for mutations associated with congenital cataracts.	Whole blood (EDTA) or buccal swab (DNA)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SORD gene mutations", "Single nucleotide variants", "Indels"] Parameters [] Preparation ["Pre-test genetic counselling is mandatory", "Share complete clinical history", "Continue prescribed medications unless advised otherwise"] Indications ["Diagnosis of SORD-related congenital cataract", "Familial screening for SORD mutations", "Genetic counselling for families with congenital cataracts"] Measurement technique Confirm with laboratory Codes LOINC: 94843-2 ICD-10: Q12.0 Clinical summary This test evaluates the SORD gene for mutations associated with congenital cataracts.
TEST-2930 SOST Gene Craniodiaphyseal Dysplasia Genetic Test This test detects pathogenic variants in the SOST gene associated with autosomal dominant craniodiaphyseal dysplasia.	Peripheral whole blood (3-5 mL EDTA) or FTA dried blood spot	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SOST gene pathogenic variants", "Autosomal dominant craniodiaphyseal dysplasia"] Parameters [] Preparation ["No specific dietary or medication modifications required", "Inform phlebotomist of anticoagulant therapy or bleeding disorders"] Indications ["Clinical features suggestive of craniodiaphyseal dysplasia", "First-degree relatives of a confirmed case"] Measurement technique Confirm with laboratory Codes LOINC: 60512-8 ICD-10: Q78.8 Clinical summary This test detects pathogenic variants in the SOST gene associated with autosomal dominant craniodiaphyseal dysplasia.
TEST-4484 SOST Gene Van Buchem Disease Genetic Test This test evaluates the SOST gene for pathogenic variants associated with Van Buchem disease (sclerosteosis). It identifies single-nucleotide variants, insertions, deletions, and c...	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 ["SOST gene variants", "Single-nucleotide variations", "Insertions/Deletions (Indels)", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["No fasting required", "No special dietary restrictions", "Mandatory pre-test genetic counselling with a three-generation pedigree chart"] Indications ["Diagnosis of Van Buchem disease (sclerosteosis)", "Differentiation from other sclerosing bone dysplasias", "Genetic counseling for individuals with suspected or confirmed Van Buchem disease", "Pre-test genetic counseling required"] Measurement technique Confirm with laboratory Codes LOINC: 83443-3 ICD-10: Q78.8 Clinical summary This test evaluates the SOST gene for pathogenic variants associated with Van Buchem disease (sclerosteosis). It identifies single-nucleotide variants, insertions, deletions, and copy number variations.
TEST-5460 SOX10 Gene Genetic Test for Peripheral Demyelinating Neuropathy, Waardenburg Syndrome & Hirschsprung Disease This test evaluates the SOX10 gene for pathogenic variants associated with peripheral demyelinating neuropathy, Waardenburg syndrome type IV, and Hirschsprung disease.	Peripheral whole blood (3 mL EDTA), extracted DNA (≥2 µg), or FTA card	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SOX10 gene sequence", "Pathogenic variants (SNVs, indels, splice-site variants, copy number variations)"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Suspected peripheral demyelinating neuropathy", "Suspected Waardenburg syndrome type IV", "Suspected Hirschsprung disease", "Family history of SOX10-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 93466-1 ICD-10: G60.0, Q87.8, Q43.1 Clinical summary This test evaluates the SOX10 gene for pathogenic variants associated with peripheral demyelinating neuropathy, Waardenburg syndrome type IV, and Hirschsprung disease.
TEST-4500 SOX10 Gene Waardenburg Syndrome Type 2E Genetic Test This genetic test identifies pathogenic variants in the SOX10 gene, confirming a diagnosis of Waardenburg syndrome type 2E.	Whole blood (3–5 mL in EDTA), Extracted DNA (≥1 μg), or one drop blood on 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 SOX10 gene", "Single nucleotide variants", "Small indels", "Exon-level deletions", "Copy number changes", "Deep intronic mutations"] Parameters [] Preparation ["No special dietary preparation needed", "Genetic counseling session recommended before sample collection"] Indications ["Confirmation of clinical diagnosis of Waardenburg syndrome type 2E", "Guidance for management of hearing loss", "Guidance for management of pigmentary abnormalities", "Genetic counseling for families"] Measurement technique Confirm with laboratory Codes LOINC: 21631-3 ICD-10: Q87.8 Clinical summary This genetic test identifies pathogenic variants in the SOX10 gene, confirming a diagnosis of Waardenburg syndrome type 2E.
TEST-4473 SOX10 Gene Waardenburg Syndrome Type 4C Genetic Test This test analyzes the SOX10 gene for mutations associated with Waardenburg syndrome type 4C.	Peripheral Whole Blood (EDTA tube) or Buccal Swab	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SOX10 gene sequence", "Pathogenic variants (SNVs, indels, CNVs)"] Parameters [] Preparation ["Informed Consent Required", "Consult physician if on anticoagulants"] Indications ["Clinical suspicion of Waardenburg syndrome type 4C", "Familial risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 94850-3 ICD-10: Q87.89 Clinical summary This test analyzes the SOX10 gene for mutations associated with Waardenburg syndrome type 4C.
TEST-4829 SOX11 Gene Mental Retardation, Autosomal Dominant Type 27 Genetic Test This test identifies pathogenic variants within the SOX11 gene, which are associated with autosomal dominant intellectual disability type 27 (MRD27). It is used to confirm a diagno...	Whole Blood (EDTA), Extracted DNA, or 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 SOX11 gene", "Single nucleotide variants", "Small insertions/deletions", "Copy number changes"] Parameters [] Preparation ["No fasting required.", "Ensure child is well-hydrated and calm for blood draw."] Indications ["Suspected Autosomal Dominant Intellectual Disability Type 27 (MRD27)", "Unexplained developmental delay", "Family history of MRD27"] Measurement technique Confirm with laboratory Codes LOINC: 92822-6 ICD-10: Q87.89 Clinical summary This test identifies pathogenic variants within the SOX11 gene, which are associated with autosomal dominant intellectual disability type 27 (MRD27). It is used to confirm a diagnosis in individuals with suspected MRD27.
TEST-3449 SOX17 Gene Vesicoureteral Reflux Type 3 Genetic Test This test identifies genetic mutations in the SOX17 gene associated with Vesicoureteral Reflux Type 3.	Peripheral whole blood	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SOX17 gene pathogenic variants", "Single nucleotide variants", "Small indels", "Copy number variations"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any relevant family history"] Indications ["Diagnosis of Vesicoureteral Reflux Type 3", "Family history of VUR3", "Assessment of familial risk"] Measurement technique Confirm with laboratory Codes LOINC: 21665-7 ICD-10: Q62.7 Clinical summary This test identifies genetic mutations in the SOX17 gene associated with Vesicoureteral Reflux Type 3.
TEST-4998 SOX18 Gene Hypotrichosis‑Lymphedema‑Telangiectasia Syndrome Genetic Test This genetic test evaluates the SOX18 gene for pathogenic variants associated with Hypotrichosis‑Lymphedema‑Telangiectasia Syndrome (HLTS).	Peripheral whole blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SOX18 gene sequence", "Pathogenic variants (SNVs, indels, CNVs)"] Parameters [] Preparation ["Pre-test genetic counselling is mandatory"] Indications ["Clinical features suggestive of HLTS", "Family history of HLTS"] Measurement technique Confirm with laboratory Codes LOINC: 88550-6 ICD-10: Q87.8 Clinical summary This genetic test evaluates the SOX18 gene for pathogenic variants associated with Hypotrichosis‑Lymphedema‑Telangiectasia Syndrome (HLTS).
TEST-3030 SOX9 Gene Campomelic Dysplasia Genetic Test This test evaluates the SOX9 gene for pathogenic variants associated with Campomelic Dysplasia.	Whole Blood, Extracted DNA, or One‑drop Blood on FTA Card	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SOX9 gene variants", "Pathogenic mutations"] Parameters [] Preparation [] Indications ["Suspected Campomelic Dysplasia", "Family history of Campomelic Dysplasia", "Reproductive risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 94228-7 ICD-10: Q77.3 Clinical summary This test evaluates the SOX9 gene for pathogenic variants associated with Campomelic Dysplasia.
TEST-3798 SP110 Gene Hepatic Veno-Occlusive Disease with Immunodeficiency Genetic Test This genetic test identifies disease-causing mutations in the SP110 gene associated with Hepatic Veno-Occlusive Disease with Immunodeficiency (VODI).	Peripheral 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 SP110 gene", "Full coding region sequencing", "Copy number analysis"] Parameters [{"name": "SP110 Gene Sequencing", "reference_range": "No pathogenic variants detected"}] Preparation ["No specific fasting required", "Inform lab of any current medications"] Indications ["Suspected VODI based on clinical presentation", "Family history of VODI", "Evaluation of combined immunodeficiency and liver disease"] Measurement technique Confirm with laboratory Codes LOINC: 81314-5 ICD-10: D84.9 Clinical summary This genetic test identifies disease-causing mutations in the SP110 gene associated with Hepatic Veno-Occlusive Disease with Immunodeficiency (VODI).
TEST-3701 Spastic Paraplegia Panel (NGS) Genetic Test This test identifies pathogenic variants in genes associated with hereditary spastic paraplegia.	Whole Blood (EDTA tube)	3–4 Weeks	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in >50 HSP genes"] Parameters [] Preparation ["No fasting required", "No medication changes required", "Complete clinical history form", "Provide family pedigree chart if possible"] Indications ["Individuals with suspected hereditary spastic paraplegia", "Family members of individuals diagnosed with HSP"] Measurement technique Confirm with laboratory Codes LOINC: 94485-8 ICD-10: G11.4 Clinical summary This test identifies pathogenic variants in genes associated with hereditary spastic paraplegia.

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

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