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

Listed price range

-1.00–50,000.00 AED

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Genetics test prices

Showing 391–405 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4825 CD27 Gene Lymphoproliferative Syndrome Type 2 (CD27 Deficiency) Genetic Test This genetic test identifies pathogenic variants in the CD27 gene, confirming a diagnosis of Lymphoproliferative Syndrome Type 2 (CD27 Deficiency).	Peripheral Whole Blood or Saliva	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 CD27 gene", "Coding region, exons, and splice sites"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any relevant medications"] Indications ["Suspected primary immunodeficiency", "Family history of CD27 deficiency", "Recurrent severe infections", "Chronic EBV viremia", "Lymphoma"] Measurement technique Confirm with laboratory Codes LOINC: 90377-2 ICD-10: D82.8 Clinical summary This genetic test identifies pathogenic variants in the CD27 gene, confirming a diagnosis of Lymphoproliferative Syndrome Type 2 (CD27 Deficiency).
TEST-5982 CD320 Gene (Methylmalonic Aciduria, cblR Type) Genetic Test This genetic test analyzes the CD320 gene to detect mutations associated with methylmalonic aciduria, cblR type.	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 ["CD320 gene sequence", "Pathogenic variants in CD320"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication"] Indications ["Suspected methylmalonic aciduria, cblR type", "Carrier screening", "Family cascade testing"] Measurement technique Confirm with laboratory Codes LOINC: 81214-4 ICD-10: E71.120 Clinical summary This genetic test analyzes the CD320 gene to detect mutations associated with methylmalonic aciduria, cblR type.
TEST-4927 CD3D Gene Immunodeficiency Type 19 Genetic Test This genetic test identifies pathogenic variants in the CD3D gene associated with primary immunodeficiency type 19.	Whole blood (EDTA), 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 ["CD3D gene sequence", "Copy Number Variations (CNVs) in CD3D gene"] Parameters [] Preparation ["No fasting required", "Provide detailed clinical summary and family pedigree if available"] Indications ["Suspected primary immunodeficiency type 19", "Family history of CD3D-related immunodeficiency"] Measurement technique Confirm with laboratory Codes LOINC: 82936-5 ICD-10: D81.2 Clinical summary This genetic test identifies pathogenic variants in the CD3D gene associated with primary immunodeficiency type 19.
TEST-4915 CD3E Gene (Immunodeficiency Type 18) Genetic Test This test evaluates the CD3E gene for variants associated with Immunodeficiency Type 18 (CD3ε deficiency), a severe combined immunodeficiency.	Peripheral Whole Blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CD3E gene sequence", "Pathogenic variants in CD3E exons"] Parameters [] Preparation ["No fasting required", "Inform physician about all medications and supplements", "Pre-test genetic counselling session is mandatory"] Indications ["Diagnosis of Immunodeficiency Type 18 (CD3ε deficiency)", "Carrier screening in families with a known CD3E variant"] Measurement technique Confirm with laboratory Codes LOINC: 101578-8 ICD-10: D81.8, D81.2, Z15.89 Clinical summary This test evaluates the CD3E gene for variants associated with Immunodeficiency Type 18 (CD3ε deficiency), a severe combined immunodeficiency.
TEST-4917 CD40 Gene Immunodeficiency Type 3 (Hyper-IgM Syndrome) Test This genetic test evaluates the CD40 gene for variants associated with Hyper-IgM syndrome type 3, a primary immunodeficiency.	Peripheral Whole Blood (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 ["CD40 gene sequence", "Detection of SNVs, indels, CNVs"] Parameters [] Preparation ["No specific fasting required", "Inform lab of anticoagulant use"] Indications ["Suspected Hyper-IgM syndrome type 3", "Recurrent sinopulmonary infections", "Opportunistic infections", "Family history of primary immunodeficiency"] Measurement technique Confirm with laboratory Codes LOINC: 94497-8 ICD-10: D82.3 Clinical summary This genetic test evaluates the CD40 gene for variants associated with Hyper-IgM syndrome type 3, a primary immunodeficiency.
TEST-4891 CD40LG Gene Immunodeficiency, X-linked with Hyper-IgM Genetic Test This test evaluates the CD40LG gene for pathogenic variants associated with X-linked hyper-IgM syndrome (HIGM1).	Peripheral Whole Blood (EDTA) or FTA Card Sample	3 – 4 weeks from sample collection	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CD40LG gene sequence", "Pathogenic variants (point mutations, deletions, insertions, deep intronic variants)"] Parameters [] Preparation [] Indications ["Clinical suspicion of X-linked hyper-IgM syndrome", "Family history consistent with X-linked inheritance", "Referral from an immunologist or genetic counselor"] Measurement technique Confirm with laboratory Codes LOINC: 96720-3 ICD-10: D82.3 Clinical summary This test evaluates the CD40LG gene for pathogenic variants associated with X-linked hyper-IgM syndrome (HIGM1).
TEST-5033 CD59 Gene Hemolytic Anemia Genetic Test This test identifies pathogenic variants in the CD59 gene associated with hemolytic anemia and immune-mediated polyneuropathy.	Whole Blood (Peripheral)	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 CD59 gene", "Molecular cause of CD59-mediated hemolytic anemia"] Parameters [] Preparation ["No fasting required"] Indications ["Clinical suspicion of CD59 deficiency", "Unexplained hemolytic anemia", "Immune-mediated polyneuropathy"] Measurement technique Confirm with laboratory Codes LOINC: 94477-0 ICD-10: D59.8 Clinical summary This test identifies pathogenic variants in the CD59 gene associated with hemolytic anemia and immune-mediated polyneuropathy.
TEST-3239 CD59 Gene Sequencing (NGS) Genetic Test This test analyzes the CD59 gene to detect pathogenic variants associated with CD59-mediated hemolytic anemia and immune-mediated polyneuropathy.	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 ["CD59 gene variants", "Single nucleotide variants", "Small insertions/deletions", "Splice-site alterations"] Parameters [] Preparation ["Avoid blood transfusion within 4 weeks prior to testing.", "Discuss medication changes with your physician before the test."] Indications ["Suspected CD59 deficiency", "Chronic hemolytic anemia of unknown cause", "Family history of CD59 deficiency", "Evaluation for complement inhibitor therapy"] Measurement technique Confirm with laboratory Codes LOINC: 90420-0 ICD-10: D59.8 Clinical summary This test analyzes the CD59 gene to detect pathogenic variants associated with CD59-mediated hemolytic anemia and immune-mediated polyneuropathy.
TEST-3381 CD79A Gene Agammaglobulinemia Type 3, Autosomal Recessive Genetic Test This genetic test analyzes the CD79A gene to detect mutations causing autosomal recessive agammaglobulinemia type 3.	2 mL EDTA whole blood 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 ["CD79A gene sequence", "Pathogenic variants in CD79A"] Parameters [] Preparation ["No fasting required"] Indications ["Clinical suspicion of agammaglobulinemia", "Family screening following genetic counselling"] Measurement technique Confirm with laboratory Codes LOINC: 21659-9 ICD-10: D80.0 Clinical summary This genetic test analyzes the CD79A gene to detect mutations causing autosomal recessive agammaglobulinemia type 3.
TEST-3339 CD79B Gene Agammaglobulinemia Type 6, Autosomal Recessive Genetic Test This diagnostic test evaluates the CD79B gene for mutations associated with autosomal recessive agammaglobulinemia type 6.	Peripheral Whole Blood or FTA Card	15–21 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CD79B gene mutations", "Presence of disease-causing variants"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any current medications"] Indications ["Suspected primary immunodeficiency", "Family history of agammaglobulinemia", "Confirmation of clinical diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 21641-6 ICD-10: D80.0 Clinical summary This diagnostic test evaluates the CD79B gene for mutations associated with autosomal recessive agammaglobulinemia type 6.
TEST-4946 CD81 Gene Immunodeficiency Common Variable Type 6 Genetic Test This test identifies pathogenic variants in the CD81 gene associated with Common Variable Immunodeficiency type 6 (CVID6).	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 CD81 gene", "Single-exon variants", "Copy-number variants"] Parameters [] Preparation [] Indications ["Suspected Common Variable Immunodeficiency type 6 (CVID6)", "Recurrent infections with low immunoglobulin levels"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: D83.8 Clinical summary This test identifies pathogenic variants in the CD81 gene associated with Common Variable Immunodeficiency type 6 (CVID6).
TEST-3014 CD96 Gene C Syndrome NGS Test This test identifies pathogenic variants in the CD96 gene associated with autosomal dominant C syndrome.	Whole blood (EDTA) or dried blood spot (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 ["CD96 gene coding region", "Pathogenic variants (SNVs, indels)"] Parameters [] Preparation [] Indications ["Suspected C syndrome", "Craniofacial anomalies", "Developmental delay"] Measurement technique Confirm with laboratory Codes LOINC: 81261-8 ICD-10: Q87.0 Clinical summary This test identifies pathogenic variants in the CD96 gene associated with autosomal dominant C syndrome.
TEST-5992 CDAN1 Gene Anemia Dyserythropoietic Type 1A Genetic Test This test evaluates the CDAN1 gene for variants associated with Congenital Dyserythropoietic Anemia Type 1A (CDA I). It identifies SNVs, indels, and copy number variations within t...	Whole Blood (EDTA), Extracted Genomic DNA, 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 ["CDAN1 gene variants", "SNVs", "Indels", "Copy Number Variations"] Parameters [] Preparation ["Do not discontinue prescribed medication without consulting haematologist"] Indications ["Suspected Congenital Dyserythropoietic Anemia Type 1A", "Family history of CDA Type I", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 81303-1 ICD-10: D64.0 Clinical summary This test evaluates the CDAN1 gene for variants associated with Congenital Dyserythropoietic Anemia Type 1A (CDA I). It identifies SNVs, indels, and copy number variations within the gene.
TEST-2106 CDC20 Gene Cell Cycle Disorder Genetic Test This genetic test evaluates the entire coding region of the CDC20 gene for variants associated with cell cycle disorders and cancer.	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 ["Single nucleotide variants (SNVs)", "Small insertions and deletions (indels)", "Copy number variations (CNVs)", "CDC20 gene sequence"] Parameters [] Preparation [] Indications ["Suspected inherited cell cycle disorder", "Cancer risk assessment", "Guidance for targeted therapy selection"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Z13.79 Clinical summary This genetic test evaluates the entire coding region of the CDC20 gene for variants associated with cell cycle disorders and cancer.
TEST-3787 CDC73 Gene (Hyperparathyroidism‑Jaw Tumor Syndrome) NGS Test This test evaluates for germline mutations within the CDC73 gene, associated with Hyperparathyroidism-Jaw Tumor Syndrome (HPT-JT). It identifies genetic predispositions to hyperpar...	Peripheral whole blood, serum, or plasma	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Germline mutations in the CDC73 gene", "Tumour suppressor gene function"] Parameters [] Preparation ["No fasting required", "No medication adjustment required"] Indications ["Diagnosis of Hyperparathyroidism-Jaw Tumor Syndrome (HPT-JT)", "Diagnosis of familial isolated hyperparathyroidism", "Risk assessment for individuals with family history of HPT-JT"] Measurement technique Confirm with laboratory Codes LOINC: 82128-6 ICD-10: E21.0 Clinical summary This test evaluates for germline mutations within the CDC73 gene, associated with Hyperparathyroidism-Jaw Tumor Syndrome (HPT-JT). It identifies genetic predispositions to hyperparathyroidism and jaw tumours.

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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