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 2536–2550 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4837 TGFBR2 Gene Loeys-Dietz Syndrome Type 1B Genetic Test This test identifies pathogenic variants in the TGFBR2 gene associated with Loeys-Dietz syndrome type 1B.	Peripheral Whole Blood (Venous 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 TGFBR2 gene", "TGF-β signalling pathway disruption"] Parameters [] Preparation [] Indications ["Clinically suspected Loeys-Dietz syndrome type 1B", "Cascade family screening"] Measurement technique Confirm with laboratory Codes LOINC: 82771-1 ICD-10: Q87.89 Clinical summary This test identifies pathogenic variants in the TGFBR2 gene associated with Loeys-Dietz syndrome type 1B.
TEST-4815 TGFBR2 Gene Loeys-Dietz Syndrome Type 2B Genetic Test This test analyzes the TGFBR2 gene for pathogenic variants associated with Loeys-Dietz syndrome type 2B.	Whole Blood (3-5 mL) or Buccal Swab	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 TGFBR2 gene", "Coding region variants", "Copy Number Variations (CNV)"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed cardiovascular medications without consulting your managing physician"] Indications ["Patients presenting with clinical features suggestive of Loeys-Dietz syndrome type 2B", "Family cascade screening for relatives of affected individuals"] Measurement technique Confirm with laboratory Codes LOINC: 81317-1 ICD-10: Q87.89 Clinical summary This test analyzes the TGFBR2 gene for pathogenic variants associated with Loeys-Dietz syndrome type 2B.
TEST-4960 TGM1 Gene Sequencing for Autosomal Recessive Congenital Ichthyosis Type 1 (ARCI1) Test This test identifies disease-causing mutations in the TGM1 gene, associated with autosomal recessive congenital ichthyosis type 1 (lamellar ichthyosis).	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 ["Pathogenic mutations in TGM1 gene coding exons", "Pathogenic mutations in TGM1 gene canonical splice sites"] Parameters [] Preparation [] Indications ["Diagnosis of lamellar ichthyosis (ARCI1)", "Carrier status identification in family members", "Informed family planning"] Measurement technique Confirm with laboratory Codes LOINC: 103231-4 ICD-10: Q80.2 Clinical summary This test identifies disease-causing mutations in the TGM1 gene, associated with autosomal recessive congenital ichthyosis type 1 (lamellar ichthyosis).
TEST-4645 TGM5 Gene (Peeling Skin Syndrome Type 2) Genetic Test This genetic test identifies pathogenic variants in the TGM5 gene to confirm a diagnosis of Peeling Skin Syndrome Type 2.	Peripheral Whole Blood	21 – 28 Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TGM5 gene", "Copy Number Variations (CNV) in the TGM5 gene"] Parameters [] Preparation ["No fasting required", "No alterations to medication routine required", "Mandatory pre-test genetic counseling session required"] Indications ["Clinical suspicion of Peeling Skin Syndrome Type 2", "Known family history of Peeling Skin Syndrome Type 2", "Family screening", "Reproductive risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 82162-7 ICD-10: Q82.8 Clinical summary This genetic test identifies pathogenic variants in the TGM5 gene to confirm a diagnosis of Peeling Skin Syndrome Type 2.
TEST-5888 TGM6 Gene Sequencing Test for Spinocerebellar Ataxia Type 35 (SCA35), Autosomal Dominant This test identifies pathogenic variants in the TGM6 gene associated with Spinocerebellar Ataxia Type 35 (SCA35). It uses Next-Generation Sequencing (NGS) with Sanger confirmation...	Whole blood (EDTA)	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 TGM6 gene", "Presence of mutations causing SCA35"] Parameters [] Preparation ["Provide detailed clinical history", "Genetic counseling with pedigree chart required"] Indications ["Diagnosis of suspected SCA35", "Genetic counseling for families with SCA35", "Predictive testing in at-risk individuals"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: G11.8 Clinical summary This test identifies pathogenic variants in the TGM6 gene associated with Spinocerebellar Ataxia Type 35 (SCA35). It uses Next-Generation Sequencing (NGS) with Sanger confirmation for high accuracy.
TEST-3262 Thalassemia Alpha Mutation Analysis Test This test identifies specific genetic mutations (deletions and point mutations) in the alpha globin genes (HBA1 and HBA2) responsible for alpha thalassemia.	Whole Blood (EDTA tube)	5 working days (Sample Mon by 9 AM → Report Fri)	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Deletions in HBA1 gene", "Deletions in HBA2 gene", "Point mutations in HBA1 gene", "Point mutations in HBA2 gene"] Parameters [] Preparation ["No fasting required", "No medication changes required unless specified by doctor", "Complete Genomics Clinical Information Requisition Form (Form 20)"] Indications ["Diagnosis of alpha thalassemia syndromes", "Identification of alpha thalassemia carriers", "Genetic counseling for families with thalassemia", "Pre-marital screening", "Prenatal diagnosis support"] Measurement technique Confirm with laboratory Codes LOINC: 49685-6 ICD-10: D56.0 Clinical summary This test identifies specific genetic mutations (deletions and point mutations) in the alpha globin genes (HBA1 and HBA2) responsible for alpha thalassemia.
TEST-3254 Thalassemia Alpha Trio Prenatal Mutation Detection Test This test evaluates the presence and type of alpha-thalassemia mutations in the fetus, parents, and amniotic fluid.	Amniotic Fluid + Parental Peripheral Blood	5 Working Days	2,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Alpha-globin gene mutations", "Alpha-thalassemia deletions"] Parameters [] Preparation ["No specific patient preparation required for blood draw.", "Amniocentesis procedure performed by obstetrician."] Indications ["Parents are known or suspected carriers of alpha-thalassemia", "Previous child affected by alpha-thalassemia", "Abnormal prenatal ultrasound findings suggestive of anemia"] Measurement technique Confirm with laboratory Codes LOINC: 56913-4 ICD-10: D56.0, Z13.0, Z15.89 Clinical summary This test evaluates the presence and type of alpha-thalassemia mutations in the fetus, parents, and amniotic fluid.
TEST-3269 Thalassemia Beta Trio Prenatal Mutation Detection Test This test evaluates the beta-globin gene in the fetus and both parents to detect mutations associated with beta-thalassaemia.	Amniotic fluid (fetal) and EDTA whole blood (parents)	5 working days	2,400.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Beta-globin gene mutations", "Fetal genotype", "Parental carrier status"] Parameters [] Preparation ["Parents provide 4 mL EDTA whole blood each", "Amniotic fluid (10 mL) collected by obstetrician", "Samples must be shipped refrigerated (2-8°C); DO NOT FREEZE"] Indications ["Families at risk for beta-thalassaemia", "Prenatal genetic screening"] Measurement technique Confirm with laboratory Codes LOINC: 21698-3 ICD-10: D56.1, O35.8XX0, Z31.430 Clinical summary This test evaluates the beta-globin gene in the fetus and both parents to detect mutations associated with beta-thalassaemia.
TEST-4270 THAP1 (DYT6) Gene Sequencing Test (NGS) This diagnostic test evaluates the THAP1 gene for pathogenic variants associated with early-onset primary dystonia (DYT6). It identifies mutations responsible for this specific mov...	Peripheral Whole Blood (EDTA tube)	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 THAP1 gene", "Single nucleotide variants (SNVs)", "Small insertions and deletions (indels)"] Parameters [{"name": "Analytical Precision", "reference_range": ">99.9% sensitivity & specificity for single nucleotide variants and small indels"}, {"name": "Methodology", "reference_range": "Next-Generation Sequencing (NGS) with full exon coverage and bioinformatics analysis"}] Preparation ["No specific fasting required", "Inform the phlebotomist of any medications being taken"] Indications ["Suspected diagnosis of early-onset primary dystonia (DYT6)", "Family history of DYT6", "Genetic counseling for dystonia"] Measurement technique Confirm with laboratory Codes LOINC: 93973-3 ICD-10: G24.1, G24.8 Clinical summary This diagnostic test evaluates the THAP1 gene for pathogenic variants associated with early-onset primary dystonia (DYT6). It identifies mutations responsible for this specific movement disorder.
TEST-3763 THBD Gene Hemolytic Uremic Syndrome Genetic Test This test analyzes the THBD gene for pathogenic variants associated with atypical hemolytic uremic syndrome (aHUS). It uses next-generation sequencing (NGS) with copy-number analys...	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 THBD gene", "Copy number variations (CNVs) in the THBD gene"] Parameters [] Preparation [] Indications ["Diagnosis of atypical hemolytic uremic syndrome (aHUS)", "Family cascade screening for THBD variants", "Guiding targeted anti-complement therapies"] Measurement technique Confirm with laboratory Codes LOINC: 21683-2 ICD-10: D59.39, Z15.89, N17.9 Clinical summary This test analyzes the THBD gene for pathogenic variants associated with atypical hemolytic uremic syndrome (aHUS). It uses next-generation sequencing (NGS) with copy-number analysis.
TEST-3740 THRA Gene Hypothyroidism Congenital Non-Goitrous Type 6 Genetic Test This test evaluates the THRA gene for pathogenic variants associated with congenital non-goitrous hypothyroidism type 6.	Whole Blood (EDTA), FTA Card, or Extracted Genomic DNA	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 THRA gene", "Single-nucleotide variants", "Small insertions/deletions", "Exon-level duplications", "Exon-level deletions", "Copy Number Variations (CNV)"] Parameters [] Preparation ["No specific fasting required.", "Inform the phlebotomist of any medications."] Indications ["Diagnosis of congenital non-goitrous hypothyroidism type 6", "Genetic counselling for families with affected individuals", "Recurrence risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: E03.1 Clinical summary This test evaluates the THRA gene for pathogenic variants associated with congenital non-goitrous hypothyroidism type 6.
TEST-5221 TIMM21 Gene Mitochondrial Respiratory Chain Disease, TIMM21-Related Genetic Test This test identifies pathogenic variants within the TIMM21 gene associated with mitochondrial respiratory chain disorders.	Whole Blood (EDTA), Dried Blood Spot (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 TIMM21 gene", "Single-nucleotide variants (SNVs)", "Insertions/Deletions (Indels)", "Gene deletions/duplications"] Parameters [] Preparation ["Pre-test genetic counseling is mandatory", "Referral from Neurologist, Medical Geneticist, or Pulmonologist is required"] Indications ["Clinical suspicion of mitochondrial respiratory chain disease", "Progressive neurological decline", "Inconclusive biochemical assays"] Measurement technique Confirm with laboratory Codes LOINC: 104204-1 ICD-10: E88.49 Clinical summary This test identifies pathogenic variants within the TIMM21 gene associated with mitochondrial respiratory chain disorders.
TEST-4567 TIMM8A Gene Jensen Syndrome Genetic Test This genetic test identifies disease-causing mutations in the TIMM8A gene associated with Jensen syndrome.	Peripheral Whole Blood (or DNA‑stabilised 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 TIMM8A gene", "Coding exons", "Flanking intronic regions", "Deep intronic hotspots"] Parameters [] Preparation ["Genetic counselling session required prior to sample collection", "No specific fasting required for blood sample"] Indications ["Clinically suspected cases of Jensen syndrome", "Family history of Jensen syndrome", "Confirmation of clinical diagnosis", "Genetic counselling for family planning"] Measurement technique Confirm with laboratory Codes LOINC: 81247-1 ICD-10: G31.8, H90.5, Z84.3 Clinical summary This genetic test identifies disease-causing mutations in the TIMM8A gene associated with Jensen syndrome.
TEST-5543 TIMM8A Gene Opticoacoustic Nerve Atrophy with Dementia Genetic Test This test analyzes the TIMM8A gene for mutations associated with Mohr-Tranebjaerg syndrome.	Peripheral 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 TIMM8A gene", "Copy Number Variations (CNVs) within the TIMM8A gene"] Parameters [] Preparation ["No specific fasting required", "Inform the phlebotomist of any medications you are taking"] Indications ["Clinical suspicion of Mohr-Tranebjaerg syndrome", "Family history of Mohr-Tranebjaerg syndrome", "Genetic counseling for at-risk individuals"] Measurement technique Confirm with laboratory Codes LOINC: 81323-0 ICD-10: G31.89 Clinical summary This test analyzes the TIMM8A gene for mutations associated with Mohr-Tranebjaerg syndrome.
TEST-6205 TJP2 Gene Hypercholanemia Genetic Test This genetic test identifies pathogenic variants in the TJP2 gene associated with progressive familial intrahepatic cholestasis type 4 (PFIC4). It helps confirm the diagnosis in pa...	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 ["Pathogenic variants in the TJP2 gene", "Bile acid transport defects"] Parameters [] Preparation ["Simple genetic counseling session", "No fasting required", "No medication changes needed"] Indications ["Confirmation of PFIC4 diagnosis", "Evaluation of unexplained cholestasis", "Assessment of liver disease progression"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: K76.8 Clinical summary This genetic test identifies pathogenic variants in the TJP2 gene associated with progressive familial intrahepatic cholestasis type 4 (PFIC4). It helps confirm the diagnosis in patients presenting with symptoms of cholestasis and liver disease.

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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