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 286–300 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-1805 Beta Thalassemia HBB Full Gene Trio Analysis (Couple & Prenatal) Test This test evaluates the HBB gene in parents and fetus to detect pathogenic mutations associated with beta-thalassemia.	Peripheral blood (parents), Amniotic fluid, Chorionic villi, or Cord blood (fetus)	8–10 working days	2,400.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["HBB gene sequence (coding and regulatory regions)", "Detection of pathogenic mutations"] Parameters [] Preparation [] Indications ["Couples with a family history of beta-thalassemia", "Consanguineous marriages", "Abnormal hemoglobin electrophoresis results", "Preconception risk assessment", "Prenatal decision-making", "Preimplantation genetic testing planning"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: D56.1, D56.3, Z14.8 Clinical summary This test evaluates the HBB gene in parents and fetus to detect pathogenic mutations associated with beta-thalassemia.
TEST-1812 Beta Thalassemia-9 Common Mutations Screening (Couple) Test This test identifies the presence of nine common beta-globin gene mutations in both partners to assess the risk of having a child with Beta Thalassemia Major.	Peripheral Blood (EDTA Whole Blood)	3–4 Days	1,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Presence of nine common beta-globin gene mutations"] Parameters [] Preparation [] Indications ["Pre-conceptional carrier screening for couples", "Family planning in high-risk populations"] Measurement technique Confirm with laboratory Codes LOINC: 49213-7 ICD-10: D56.1 Clinical summary This test identifies the presence of nine common beta-globin gene mutations in both partners to assess the risk of having a child with Beta Thalassemia Major.
TEST-2254 BHLHA9 Gene Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction Genetic Test This test evaluates the BHLHA9 gene for mutations associated with mesoaxial synostotic syndactyly with phalangeal reduction.	Whole Blood, 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 ["BHLHA9 gene sequence", "Pathogenic variants (SNVs, indels, CNVs)"] Parameters [] Preparation ["No specific fasting required", "Avoid sample collection during acute illness"] Indications ["Suspected mesoaxial synostotic syndactyly with phalangeal reduction", "Genetic confirmation of clinical diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 94228-7 ICD-10: Q87.2 Clinical summary This test evaluates the BHLHA9 gene for mutations associated with mesoaxial synostotic syndactyly with phalangeal reduction.
TEST-3503 BICC1 Gene Renal Cystic Dysplasia Susceptibility Test This test identifies pathogenic variants in the BICC1 gene associated with renal cystic dysplasia susceptibility.	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 BICC1 gene"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting your doctor"] Indications ["Screening for BICC1-related renal cystic dysplasia", "Diagnosis in individuals with suspected hereditary renal-hepatic disorders", "Genetic counselling for at-risk families"] Measurement technique Confirm with laboratory Codes LOINC: 21626-0 ICD-10: Q61.4 Clinical summary This test identifies pathogenic variants in the BICC1 gene associated with renal cystic dysplasia susceptibility.
TEST-3955 BIN1 Gene Centronuclear Myopathy Type 2 Genetic Test This genetic test analyzes the BIN1 gene for mutations associated with Centronuclear Myopathy Type 2.	Whole blood (EDTA), 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 BIN1 gene", "Presence of mutations causing CNM2"] Parameters [] Preparation ["Mandatory genetic counseling session prior to sample collection", "Written informed consent required"] Indications ["Clinical suspicion of Centronuclear Myopathy Type 2", "Family history of CNM2", "Carrier screening in families with CNM2"] Measurement technique Confirm with laboratory Codes LOINC: 81315-1 ICD-10: G71.2 Clinical summary This genetic test analyzes the BIN1 gene for mutations associated with Centronuclear Myopathy Type 2.
TEST-3403 Blood Coagulation Panel Genetic Test This test evaluates 84 genes for mutations associated with inherited bleeding, thrombotic, and platelet disorders.	Peripheral whole blood	3–4 weeks from sample receipt	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Genetic variants in 84 coagulation-related genes", "Presence of mutations causing inherited bleeding or clotting disorders"] Parameters [] Preparation ["No fasting required", "Pre-test genetic counseling session is mandatory (conducted via telemedicine)"] Indications ["Diagnosis of inherited bleeding disorders (e.g., haemophilia, von Willebrand disease)", "Diagnosis of inherited thrombophilia", "Family risk assessment for coagulation disorders", "Personalized treatment planning"] Measurement technique Confirm with laboratory Codes LOINC: 81305-8 ICD-10: D68.9 Clinical summary This test evaluates 84 genes for mutations associated with inherited bleeding, thrombotic, and platelet disorders.
TEST-3388 BMP15 Gene Ovarian Dysgenesis Type 2 (OD2) Genetic Test This test analyzes the BMP15 gene for pathogenic variants associated with Ovarian Dysgenesis Type 2 (OD2) using Next-Generation Sequencing (NGS). It provides definitive molecular c...	Whole Blood / FTA Card / Extracted DNA	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["BMP15 gene coding regions", "Adjacent intronic boundaries of BMP15 gene"] Parameters [] Preparation ["No specific preparation required"] Indications ["Diagnosis of Ovarian Dysgenesis Type 2", "Familial risk assessment for OD2", "Guidance for fertility preservation", "Guidance for hormone therapy decisions"] Measurement technique Confirm with laboratory Codes LOINC: 21659-3 ICD-10: Q50.0 Clinical summary This test analyzes the BMP15 gene for pathogenic variants associated with Ovarian Dysgenesis Type 2 (OD2) using Next-Generation Sequencing (NGS). It provides definitive molecular confirmation for familial risk assessment and clinical management.
TEST-2472 BMP4 Gene Genetic Test (Orofacial Cleft Type 11) This diagnostic test evaluates the BMP4 gene for pathogenic variants associated with nonsyndromic orofacial cleft type 11.	Peripheral whole blood (EDTA) or buccal swab / FTA card	3–4 weeks (12–16 business days)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the BMP4 gene", "Full coding region and splice sites coverage"] Parameters [] Preparation ["No fasting required", "Inform doctor of all prescribed drugs"] Indications ["Diagnosis of nonsyndromic orofacial cleft type 11", "Familial risk assessment", "Tailored surgical planning", "Prenatal testing guidance"] Measurement technique Confirm with laboratory Codes LOINC: 98527-6 ICD-10: Q37.9 Clinical summary This diagnostic test evaluates the BMP4 gene for pathogenic variants associated with nonsyndromic orofacial cleft type 11.
TEST-2034 BMPR1A Gene Juvenile Polyposis Syndrome Genetic Test This test evaluates the BMPR1A gene for mutations associated with Juvenile Polyposis Syndrome (JPS), a hereditary condition increasing colorectal cancer risk.	Peripheral 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 ["BMPR1A gene mutations", "Single nucleotide variants", "Small insertions/deletions", "Copy number changes"] Parameters [] Preparation ["Genetic counselling session is mandatory before sample collection"] Indications ["Individuals with multiple juvenile polyps", "Family history of JPS or early-onset colorectal cancer", "Suspected hereditary polyposis", "Asymptomatic individuals with a known family mutation"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q85.09 Clinical summary This test evaluates the BMPR1A gene for mutations associated with Juvenile Polyposis Syndrome (JPS), a hereditary condition increasing colorectal cancer risk.
TEST-3023 BMPR1B Gene Brachydactyly Type A2 Genetic Test This test identifies pathogenic variants in the BMPR1B gene associated with Brachydactyly Type A2.	Peripheral Whole Blood 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 ["BMPR1B gene coding region", "Splice sites"] Parameters [] Preparation [] Indications ["Suspected Brachydactyly Type A2", "Family history of autosomal dominant skeletal dysplasia", "Genetic counseling", "Family planning"] Measurement technique Confirm with laboratory Codes LOINC: 21635-7 ICD-10: Q73.8 Clinical summary This test identifies pathogenic variants in the BMPR1B gene associated with Brachydactyly Type A2.
TEST-2968 BMPR1B Gene Sequencing (NGS) Test This test evaluates the BMPR1B gene for pathogenic variants associated with acromesomelic chondrodysplasia with genital anomalies (AMCD2B).	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 ["BMPR1B gene coding region variants", "Pathogenic mutations"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any medications"] Indications ["Suspected acromesomelic chondrodysplasia with genital anomalies (AMCD2B)", "Genetic counselling for families with affected individuals"] Measurement technique Confirm with laboratory Codes LOINC: 82394-1 ICD-10: Q77.8 Clinical summary This test evaluates the BMPR1B gene for pathogenic variants associated with acromesomelic chondrodysplasia with genital anomalies (AMCD2B).
TEST-3963 BMPR2 Gene Pulmonary Veno-Occlusive Disease Type 1 Genetic Test This test evaluates the BMPR2 gene for pathogenic variants associated with pulmonary veno-occlusive disease and heritable pulmonary arterial hypertension.	Whole Blood, DNA, 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 BMPR2 gene", "Single nucleotide variants (SNVs)", "Insertions and deletions (Indels)", "Copy number variations (CNVs)"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of current medications, especially anticoagulants"] Indications ["Diagnosis of pulmonary veno-occlusive disease (PVOD)", "Diagnosis of heritable pulmonary arterial hypertension (HPAH)", "Familial risk assessment for PVOD/HPAH", "Cascade testing in families with known BMPR2 mutations"] Measurement technique Confirm with laboratory Codes LOINC: 48002-0 ICD-10: I27.0, I27.20, Z15.09 Clinical summary This test evaluates the BMPR2 gene for pathogenic variants associated with pulmonary veno-occlusive disease and heritable pulmonary arterial hypertension.
TEST-4003 BMPR2 Gene Test This test identifies pathogenic variants in the BMPR2 gene associated with heritable pulmonary arterial hypertension (HPAH).	Peripheral whole blood, 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 BMPR2 gene", "DNA sequence coverage of coding, intronic, and regulatory regions"] Parameters [] Preparation ["A formal genetic counselling session is mandatory before sample collection.", "A three-generation pedigree must be completed before sample collection."] Indications ["Diagnosis of heritable pulmonary arterial hypertension (HPAH)", "Family risk assessment for HPAH", "Cascade testing in at-risk relatives"] Measurement technique Confirm with laboratory Codes LOINC: 21643-5 ICD-10: I27.0 Clinical summary This test identifies pathogenic variants in the BMPR2 gene associated with heritable pulmonary arterial hypertension (HPAH).
TEST-1757 Bone Marrow Failure Syndrome Genetic Panel Test This test identifies genetic mutations associated with inherited bone marrow failure syndromes using next-generation sequencing.	Peripheral whole blood (2× EDTA tubes)	4–6 weeks	4,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in genes linked to inherited bone marrow failure (e.g., FANCA, DKC1, TERT, SBDS)", "Genetic predisposition to bone marrow failure syndromes"] Parameters [] Preparation ["No fasting or special preparation is required", "Phlebotomist will collect a peripheral blood sample"] Indications ["Diagnosis of suspected inherited bone marrow failure syndromes", "Prognosis assessment", "Family planning and genetic counselling"] Measurement technique Confirm with laboratory Codes LOINC: 81319-8 ICD-10: D61.9 Clinical summary This test identifies genetic mutations associated with inherited bone marrow failure syndromes using next-generation sequencing.
TEST-1754 Bone Marrow Karyotyping Analysis Test This test analyzes the chromosomes within bone marrow cells to detect abnormalities associated with blood cancers and genetic disorders.	Bone marrow aspirate	7–8 days	550.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal number", "Chromosomal structure"] Parameters [] Preparation ["Stop blood thinners 5 days prior after consulting your physician", "Fast for 6 hours", "Arrange for someone to drive you home post-procedure", "A valid DHA-licensed physician’s prescription is mandatory"] Indications ["Diagnosis of leukemia (AML, CML, ALL)", "Diagnosis of myelodysplastic syndromes (MDS)", "Diagnosis of myeloproliferative neoplasms (MPN)", "Workup for recurrent pregnancy loss", "Investigation of constitutional genetic syndromes"] Measurement technique Confirm with laboratory Codes LOINC: 623-7 ICD-10: Z01.89 Clinical summary This test analyzes the chromosomes within bone marrow cells to detect abnormalities associated with blood cancers and genetic disorders.

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

Genetics: overview

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