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 2461–2475 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4964 STS Gene (X-Linked Ichthyosis) Genetic Test This test identifies pathogenic variants in the STS gene associated with X-linked ichthyosis.	Peripheral Whole Blood	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 ["Pathogenic variants in the STS gene", "Steroid Sulfatase gene sequence"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any medications"] Indications ["Suspected X-linked ichthyosis", "Family history of X-linked ichthyosis", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 94222-4 ICD-10: Q80.1 Clinical summary This test identifies pathogenic variants in the STS gene associated with X-linked ichthyosis.
TEST-6278 STT3A Gene Congenital Disorder of Glycosylation Type Iw Genetic Test This genetic test identifies pathogenic variants in the STT3A gene, confirming a diagnosis of Congenital Disorder of Glycosylation Type Iw (CDG-Iw).	Whole Blood (EDTA tube, 3–5 mL), Extracted DNA (minimum 1 µg at ≥50 ng/µL), or One Drop of Blood on FTA Card	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["STT3A gene sequence", "Pathogenic variants in STT3A"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any relevant medications"] Indications ["Unexplained global developmental delay", "Axial hypotonia", "Abnormal coagulation profiles", "Characteristic type 1 transferrin isoform pattern", "Consanguinity", "Positive family history consistent with autosomal recessive inheritance"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: E77.8 Clinical summary This genetic test identifies pathogenic variants in the STT3A gene, confirming a diagnosis of Congenital Disorder of Glycosylation Type Iw (CDG-Iw).
TEST-5057 STX11 Gene Hemophagocytic Lymphohistiocytosis Type 4 (FHL4) Genetic Test This test analyzes the STX11 gene for mutations associated with Familial Hemophagocytic Lymphohistiocytosis Type 4 (FHL4). It identifies pathogenic variants to confirm diagnosis an...	Peripheral Whole Blood 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 ["Pathogenic mutations in the STX11 gene", "Copy number variations (deletions/duplications) in the STX11 gene"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions"] Indications ["Suspected primary HLH cases", "Individuals with symptoms suggestive of FHL4", "Carrier screening in families with known STX11 mutations", "Evaluation of asymptomatic siblings in affected families"] Measurement technique Confirm with laboratory Codes LOINC: 94533-7 ICD-10: D76.1 Clinical summary This test analyzes the STX11 gene for mutations associated with Familial Hemophagocytic Lymphohistiocytosis Type 4 (FHL4). It identifies pathogenic variants to confirm diagnosis and guide management.
TEST-4518 STX1B Gene Generalized Epilepsy with Febrile Seizures Plus Type 9 Genetic Test This test analyzes the STX1B gene for mutations associated with generalized epilepsy with febrile seizures plus (GEFS+) type 9.	Whole blood (EDTA) or FTA card finger-prick	3 to 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["STX1B gene sequence", "Pathogenic variants (SNVs, indels)"] Parameters [] Preparation ["No fasting required", "Continue all prescribed medications"] Indications ["Suspected GEFS+ type 9", "Family history of GEFS+", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 85443-8 ICD-10: G40.3, R56.0 Clinical summary This test analyzes the STX1B gene for mutations associated with generalized epilepsy with febrile seizures plus (GEFS+) type 9.
TEST-5025 STXBP2 Gene Hemophagocytic Lymphohistiocytosis Type 5 Genetic Test This genetic test identifies pathogenic variants in the STXBP2 gene associated with Familial Hemophagocytic Lymphohistiocytosis Type 5 (FHL5).	Whole Blood (EDTA tube, 3–5 mL), Extracted DNA (≥1 µg at ≥50 ng/µL), 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 ["STXBP2 gene sequence", "Pathogenic variants in STXBP2"] Parameters [] Preparation ["Clinical history documentation", "Genetic counselling session with pedigree chart"] Indications ["Suspected Familial Hemophagocytic Lymphohistiocytosis Type 5", "Carrier screening for reproductive planning", "Screening presymptomatic family members"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: D76.1 Clinical summary This genetic test identifies pathogenic variants in the STXBP2 gene associated with Familial Hemophagocytic Lymphohistiocytosis Type 5 (FHL5).
TEST-5188 SUCLA2 Gene Mitochondrial DNA Depletion Syndrome Genetic Test This genetic test analyzes the SUCLA2 gene for pathogenic variants associated with mitochondrial DNA depletion syndrome type 5 (MTDPS5).	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 SUCLA2 gene", "Full gene coverage", "Deep intronic mutations", "Copy Number Variations (CNV)"] Parameters [] Preparation ["No specific fasting required.", "Do not discontinue prescribed medications unless instructed by a physician."] Indications ["Infants or children with hypotonia, developmental delay, and elevated methylmalonic acid.", "Suspected mitochondrial DNA depletion syndrome type 5 (MTDPS5)."] Measurement technique Confirm with laboratory Codes LOINC: 21730-8 ICD-10: E88.49 Clinical summary This genetic test analyzes the SUCLA2 gene for pathogenic variants associated with mitochondrial DNA depletion syndrome type 5 (MTDPS5).
TEST-5109 SUCLG1 Gene Genetic Test for Mitochondrial DNA Depletion Syndrome (Encephalomyopathic Type with Methylmalonic Aciduria) This test identifies pathogenic variants in the SUCLG1 gene associated with a specific type of mitochondrial DNA depletion syndrome.	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 ["SUCLG1 gene variants", "Pathogenic mutations"] Parameters [] Preparation ["Mandatory Genetic Counseling session prior to sample collection", "Disclose all current medications, supplements, and recent illnesses", "Complete mandatory medication disclosure form"] Indications ["Infants and children with symptoms suggestive of the disorder", "Asymptomatic siblings and extended family members seeking carrier status", "Adults with unexplained mitochondrial myopathy and compatible biochemical profile"] Measurement technique Confirm with laboratory Codes LOINC: 94233-3 ICD-10: E88.49 Clinical summary This test identifies pathogenic variants in the SUCLG1 gene associated with a specific type of mitochondrial DNA depletion syndrome.
TEST-2141 SUFU Gene Basal Cell Nevus Syndrome Genetic Test This test evaluates the SUFU gene for pathogenic variants associated with Nevoid Basal Cell Carcinoma Syndrome (Gorlin syndrome).	Peripheral Whole Blood (EDTA) 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 SUFU gene", "Full coding region and adjacent splice sites of the SUFU gene"] Parameters [] Preparation ["Mandatory pre-test genetic counselling", "Three-generation pedigree assessment"] Indications ["Diagnosis of Nevoid Basal Cell Carcinoma Syndrome (Gorlin syndrome)", "Family cascade screening for Gorlin syndrome", "Evidence-based surveillance for associated cancers"] Measurement technique Confirm with laboratory Codes LOINC: 90278-2 ICD-10: Q85.01 Clinical summary This test evaluates the SUFU gene for pathogenic variants associated with Nevoid Basal Cell Carcinoma Syndrome (Gorlin syndrome).
TEST-2029 SUFU Gene Sequencing for Familial Desmoplastic Medulloblastoma (NGS) Test This test analyzes the SUFU gene for germline pathogenic variants associated with familial desmoplastic medulloblastoma.	Whole Blood (EDTA tube), Extracted Genomic DNA (≥3 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 ["SUFU gene coding region", "Germline pathogenic variants"] Parameters [] Preparation [] Indications ["Individuals with personal or family history of medulloblastoma", "Asymptomatic relatives of affected individuals"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: Z15.09, C71.6 Clinical summary This test analyzes the SUFU gene for germline pathogenic variants associated with familial desmoplastic medulloblastoma.
TEST-3533 SULT2B1 Gene Polycystic Ovary Syndrome Type 1 Genetic Test This genetic test identifies pathogenic variants within the SULT2B1 gene associated with Polycystic Ovary Syndrome Type 1.	Peripheral Blood (FTA Card or Venous)	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 SULT2B1 gene", "Steroid sulfation pathway disruption"] Parameters [] Preparation ["No fasting required", "Provide complete clinical history", "Genetic counseling session required"] Indications ["Diagnosis of PCOS Type 1", "Risk assessment for PCOS Type 1", "Family history of PCOS"] Measurement technique Confirm with laboratory Codes LOINC: 82610-3 ICD-10: E28.2 Clinical summary This genetic test identifies pathogenic variants within the SULT2B1 gene associated with Polycystic Ovary Syndrome Type 1.
TEST-5808 SUMF1 Gene Sulfatase Deficiency Genetic Test This genetic test evaluates the SUMF1 gene for pathogenic variants associated with Multiple Sulfatase Deficiency (MSD). It identifies mutations, deletions, and duplications within...	Peripheral whole blood (5 ml in EDTA tube) or Buccal Swab	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SUMF1 gene sequence", "Copy number variations (CNVs) in SUMF1 gene"] Parameters [] Preparation ["No fasting required", "Simple blood draw or buccal swab sufficient"] Indications ["Suspected Multiple Sulfatase Deficiency (MSD)", "Carrier screening in families with MSD", "Prenatal diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 94222-8 ICD-10: E75.26 Clinical summary This genetic test evaluates the SUMF1 gene for pathogenic variants associated with Multiple Sulfatase Deficiency (MSD). It identifies mutations, deletions, and duplications within the gene.
TEST-2488 SUMO1 Gene Orofacial Cleft Type 10 Genetic Test This test evaluates the SUMO1 gene for pathogenic variants associated with orofacial cleft type 10.	Peripheral 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 SUMO1 gene", "Single-nucleotide variants (SNVs)", "Small insertions and deletions (indels)", "Copy-number alterations (CNVs)", "Deep intronic variants"] Parameters [] Preparation ["No fasting required", "No discontinuation of medications required"] Indications ["Infants or children diagnosed with orofacial cleft", "Individuals with a strong family history of clefting", "Couples planning a pregnancy seeking carrier or recurrence risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q37.9 Clinical summary This test evaluates the SUMO1 gene for pathogenic variants associated with orofacial cleft type 10.
TEST-5665 SUN1 Gene Genetic Test for Autosomal Recessive Deafness This test identifies pathogenic variants in the SUN1 gene associated with autosomal recessive non-syndromic sensorineural hearing loss.	Peripheral Whole Blood (3-5 mL in EDTA tube) or 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 ["SUN1 gene sequence", "Pathogenic variants (point mutations, small insertions/deletions, copy number variations)"] Parameters [] Preparation ["No fasting required", "Provide detailed hearing-loss history", "Attend a genetic counseling session beforehand", "Inform of any recent blood transfusions"] Indications ["Diagnosis of autosomal recessive non-syndromic sensorineural hearing loss", "Family planning for individuals with a family history of hearing loss", "Genetic counseling for hearing loss"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: H90.3, H90.41, H90.42 Clinical summary This test identifies pathogenic variants in the SUN1 gene associated with autosomal recessive non-syndromic sensorineural hearing loss.
TEST-5869 SUOX Gene Sulfite Oxidase Deficiency Genetic Test This test detects mutations in the SUOX gene associated with sulfite oxidase deficiency.	Whole Blood, DNA 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 ["SUOX gene mutations", "Disease-causing variants"] Parameters [] Preparation [] Indications ["Suspected sulfite oxidase deficiency", "Family history of metabolic disorders", "Genetic counselling"] Measurement technique Confirm with laboratory Codes LOINC: 81247-0 ICD-10: E72.1, Z15.89, Z13.79 Clinical summary This test detects mutations in the SUOX gene associated with sulfite oxidase deficiency.
TEST-4651 SURF1 Gene Analysis (Leigh Syndrome, COX Deficiency) Test This test identifies pathogenic variants within the SURF1 gene associated with Leigh syndrome and cytochrome c oxidase (COX) deficiency.	Peripheral whole blood (3–5 mL in EDTA tube); alternative buccal swab accepted for paediatric cases	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SURF1 gene sequence", "Pathogenic variants (SNVs, indels, CNVs)"] Parameters [] Preparation ["No special dietary preparation required", "Bring valid Emirates ID or passport", "Bring prior neurological imaging reports", "Bring previous genetic testing records", "Bring a complete list of current medications"] Indications ["Suspected Leigh syndrome", "Suspected mitochondrial disorder", "Cytochrome c oxidase (COX) deficiency"] Measurement technique Confirm with laboratory Codes LOINC: 101388-0 ICD-10: G31.82 Clinical summary This test identifies pathogenic variants within the SURF1 gene associated with Leigh syndrome and cytochrome c oxidase (COX) deficiency.

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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