Diagnostic options · UAE

Genetic tests in Dubai & UAE

Compare available Genetic tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

Tests in this category

805

Listed price range

600.00–30,000.00 AED

Clinical preparation

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Genetic test prices

Showing 241–255 of 805 matching tests.

Genetic diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4353 EMD Gene (Emery-Dreifuss Muscular Dystrophy Type 1) NGS Test This test analyzes the entire EMD gene for mutations associated with Emery-Dreifuss muscular dystrophy type 1.	Peripheral whole blood (EDTA) 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 EMD gene", "Single nucleotide variants (SNVs)", "Insertions/deletions (Indels)", "Copy number variations (CNVs)"] Parameters [] Preparation ["No special preparation is required."] Indications ["Diagnosis of Emery-Dreifuss muscular dystrophy type 1", "Carrier status testing in at-risk family members", "Genetic counseling for families with EDMD1"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: G71.0 Clinical summary This test analyzes the entire EMD gene for mutations associated with Emery-Dreifuss muscular dystrophy type 1.
TEST-6349 ENO3 Gene Glycogen Storage Disease Type 13 (GSD XIII) Genetic Test This test evaluates the entire ENO3 gene for mutations associated with Glycogen Storage Disease Type 13 (GSD XIII). It identifies pathogenic variants, including single nucleotide v...	Peripheral Whole Blood (EDTA) or FTA Dried Blood Spot	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ENO3 gene sequence", "Copy Number Variants (CNVs) in ENO3 gene"] Parameters [] Preparation ["No special preparation such as fasting is required."] Indications ["Suspected Glycogen Storage Disease Type 13", "Unexplained exercise intolerance", "Recurrent muscle cramps"] Measurement technique Confirm with laboratory Codes LOINC: 77784-8 ICD-10: E74.09 Clinical summary This test evaluates the entire ENO3 gene for mutations associated with Glycogen Storage Disease Type 13 (GSD XIII). It identifies pathogenic variants, including single nucleotide variants, insertions/deletions, and copy number variations.
TEST-4081 ENPP1 Gene Arterial Calcification Type 1 (GACI) Genetic Test This genetic test identifies pathogenic variants in the ENPP1 gene, confirming a diagnosis of Generalized Arterial Calcification of Infancy (GACI) type 1.	Peripheral Whole Blood	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 ENPP1 gene"] Parameters [] Preparation ["No fasting required.", "Pediatric phlebotomist will collect a small blood sample."] Indications ["Infants with suspected GACI type 1", "Family history of GACI type 1", "Genetic counseling for at-risk families"] Measurement technique Confirm with laboratory Codes LOINC: 88518-0 ICD-10: Q28.2 Clinical summary This genetic test identifies pathogenic variants in the ENPP1 gene, confirming a diagnosis of Generalized Arterial Calcification of Infancy (GACI) type 1.
TEST-5314 ENPP1 Gene Cole Disease Genetic Test This genetic test analyzes the ENPP1 gene for mutations associated with Cole disease.	Whole blood (EDTA), extracted DNA, or FTA card	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 ENPP1 gene", "Coding regions and splice sites of the ENPP1 gene"] Parameters [] Preparation ["No fasting required", "Complete a pre-test genetic counseling session", "Provide a detailed three-generation family pedigree"] Indications ["Suspected Cole disease based on clinical presentation", "Family history suggestive of Cole disease"] Measurement technique Confirm with laboratory Codes LOINC: 98349-2 ICD-10: Q82.8, Z15.89, Z13.79 Clinical summary This genetic test analyzes the ENPP1 gene for mutations associated with Cole disease.
TEST-6254 Enterokinase Deficiency (TMPRSS15 Gene) Genetic Test This genetic test analyzes the entire coding sequence and CNVs of the TMPRSS15 gene to detect pathogenic variants causing congenital enterokinase deficiency.	Peripheral whole blood (2–5 mL in EDTA) or buccal swab (infants)	3–4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TMPRSS15 gene", "Single nucleotide variants (SNV)", "Small insertions/deletions (indel)", "Copy number variants (CNV)"] Parameters [] Preparation ["No specific fasting required.", "Inform the lab of any relevant family history."] Indications ["Infants or children presenting with unexplained hypoproteinaemia, oedema, and growth faltering.", "Confirmation of suspected congenital enterokinase deficiency.", "Identification of pathogenic variants in the TMPRSS15 gene.", "Family planning for families with an affected child."] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: E88.89 Clinical summary This genetic test analyzes the entire coding sequence and CNVs of the TMPRSS15 gene to detect pathogenic variants causing congenital enterokinase deficiency.
TEST-5432 EOGT Gene Adams-Oliver Syndrome Type 4 Genetic Test This test identifies pathogenic variants in the EOGT gene associated with Adams-Oliver syndrome type 4.	Peripheral whole blood (or pre-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 EOGT gene", "Copy Number Variations (CNV) in the EOGT gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Clinical features suggestive of Adams-Oliver syndrome type 4", "Family history of Adams-Oliver syndrome type 4", "Genetic counselling recommendation"] Measurement technique Confirm with laboratory Codes LOINC: 95887-3 ICD-10: Q87.2, Q84.8, Z13.79 Clinical summary This test identifies pathogenic variants in the EOGT gene associated with Adams-Oliver syndrome type 4.
TEST-3287 EPAS1 Gene Erythrocytosis (Familial Type 4) Genetic Test This test evaluates the EPAS1 gene for mutations associated with familial erythrocytosis type 4.	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 ["EPAS1 gene sequence", "Copy Number Variations (CNV) in EPAS1"] Parameters [] Preparation ["Detailed clinical history including prior hematological events and family history of erythrocytosis.", "Mandatory genetic counselling session to construct a pedigree chart."] Indications ["Suspected familial erythrocytosis type 4", "Family screening for EPAS1 mutations"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: D75.0, D75.1, Z15.89 Clinical summary This test evaluates the EPAS1 gene for mutations associated with familial erythrocytosis type 4.
TEST-6255 EPHX2 Gene Modifier Analysis for Familial Hypercholesterolemia (LDLR Defect) via NGS Test This test analyzes the EPHX2 gene to identify variants that modify the severity and drug response associated with LDLR-related familial hypercholesterolemia.	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 ["EPHX2 gene variants", "Modifier effect on LDL receptor activity", "Cardiovascular risk prediction"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed lipid-lowering medication"] Indications ["In-depth lipid disorder phenotyping", "Tailored statin or intensive therapy decisions", "Screening suspected familial hypercholesterolemia cases", "Risk prediction studies"] Measurement technique Confirm with laboratory Codes LOINC: 88214-3 ICD-10: E78.01 Clinical summary This test analyzes the EPHX2 gene to identify variants that modify the severity and drug response associated with LDLR-related familial hypercholesterolemia.
TEST-1055 Episodic Ataxia Type 2 Hotspot Test This test identifies specific pathogenic mutations in the CACNA1A gene associated with Episodic Ataxia Type 2 (EA2). It is used for definitive diagnosis in patients presenting with...	Whole Blood (Lavender Top EDTA Tube, 2 mL min)	5 Business Days	1,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic mutations in the CACNA1A gene", "Presence of known EA2 hotspot variants"] Parameters [] Preparation ["No fasting required", "Collect 2 mL whole blood in a Lavender Top (EDTA) tube", "Refrigerate sample immediately", "Ship via temperature-controlled cold-chain logistics"] Indications ["Clinical suspicion of Episodic Ataxia Type 2", "Documented family history of EA2", "Differential diagnosis of ataxia, vertigo, or migraine"] Measurement technique Confirm with laboratory Codes LOINC: 21631-6 ICD-10: G11.8 Clinical summary This test identifies specific pathogenic mutations in the CACNA1A gene associated with Episodic Ataxia Type 2 (EA2). It is used for definitive diagnosis in patients presenting with characteristic symptoms.
TEST-3839 ESR1 Gene Estrogen Resistance Genetic Test This genetic test identifies pathogenic variants in the ESR1 gene associated with estrogen resistance.	Peripheral Whole Blood	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 ESR1 gene", "Estrogen receptor alpha gene mutations"] Parameters [] Preparation [] Indications ["Family history of estrogen resistance", "Endocrinologists seeking personalised hormone therapy guidance", "Fertility specialists investigating unexplained infertility", "Anti-aging physicians exploring hormone optimisation"] Measurement technique Confirm with laboratory Codes LOINC: 93026-2 ICD-10: Z15.89 Clinical summary This genetic test identifies pathogenic variants in the ESR1 gene associated with estrogen resistance.
TEST-4399 ETHE1 Gene Ethylmalonic Encephalopathy Genetic Test This test identifies pathogenic variants in the ETHE1 gene associated with ethylmalonic encephalopathy.	Whole Blood, Extracted DNA, Dried Blood Spot	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ETHE1 gene coding exons", "ETHE1 gene conserved splice sites"] Parameters [] Preparation ["No specific fasting required", "Avoid blood collection during acute illness"] Indications ["Suspected ethylmalonic encephalopathy", "Family history of ethylmalonic encephalopathy", "Unexplained neurological symptoms"] Measurement technique Confirm with laboratory Codes LOINC: 95207-8 ICD-10: E72.51 Clinical summary This test identifies pathogenic variants in the ETHE1 gene associated with ethylmalonic encephalopathy.
TEST-3142 ETV6 Gene Thrombocytopenia Type 5 Genetic Test This test evaluates the ETV6 gene for variants associated with hereditary thrombocytopenia type 5.	Peripheral whole blood (EDTA)	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)", "Insertions/deletions (indels)", "Copy number variations (CNVs)", "Full ETV6 gene sequence"] Parameters [] Preparation ["No fasting required", "No medication changes required", "Genetic counseling session recommended"] Indications ["Suspected hereditary thrombocytopenia type 5", "Evaluation of bleeding risk", "Family history of ETV6-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 76905-3 ICD-10: D69.41 Clinical summary This test evaluates the ETV6 gene for variants associated with hereditary thrombocytopenia type 5.
TEST-5084 EXT1 Gene Exostoses, Multiple, Type 1 Test This test evaluates the EXT1 gene for pathogenic variants associated with Hereditary Multiple Exostoses (Type 1). It identifies genetic mutations linked to the development of multi...	Whole blood (EDTA) 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 EXT1 gene", "Copy Number Variations (CNV) in EXT1"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication"] Indications ["Confirmation of clinical diagnosis of Hereditary Multiple Exostoses (Type 1)", "Genetic counselling for families with HME", "Guiding surveillance strategies"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q78.6 Clinical summary This test evaluates the EXT1 gene for pathogenic variants associated with Hereditary Multiple Exostoses (Type 1). It identifies genetic mutations linked to the development of multiple benign bone tumors (osteochondromas).
TEST-5795 EYA1 Gene Branchiootic Syndrome Type 1 Genetic Test This test identifies pathogenic variants in the EYA1 gene to diagnose Branchiootic Syndrome Type 1.	Whole Blood (EDTA, 3–5 mL) or Extracted DNA (≥1 µg, A260/A280: 1.8–2.0)	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 EYA1 gene", "Full coding region + splice sites"] Parameters [{"name": "EYA1 Gene Analysis", "reference_range": "No pathogenic variants detected"}] Preparation ["Discontinue high-dose biotin (>5 mg/day) supplementation 72 hours prior to blood draw."] Indications ["Congenital ear anomalies", "Branchial cleft fistulae", "Preauricular tags", "Guiding otologic surgical planning", "Audiological rehabilitation", "Familial genetic risk stratification"] Measurement technique Confirm with laboratory Codes LOINC: 94219-4 ICD-10: Q87.0 Clinical summary This test identifies pathogenic variants in the EYA1 gene to diagnose Branchiootic Syndrome Type 1.
TEST-3835 F12 Gene (Factor XII Deficiency) Genetic Test This genetic test evaluates the F12 gene for mutations associated with Factor XII deficiency and Hereditary Angioedema type III.	Peripheral Whole Blood	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 F12 gene", "Carrier status for F12 gene mutations", "Risk for Hereditary Angioedema type III (HAE-FXII)"] Parameters [{"name": "Analytical Sensitivity", "reference_range": ">99.9%"}, {"name": "Analytical Specificity", "reference_range": ">99.9%"}] Preparation ["No specific fasting required", "Consult your doctor regarding medication adjustments"] Indications ["Diagnosis of hereditary Factor XII deficiency", "Diagnosis of Hereditary Angioedema type III (HAE-FXII)", "Identification of carriers for F12 gene mutations", "Family screening for F12 gene mutations"] Measurement technique Confirm with laboratory Codes LOINC: 21636-3 ICD-10: D68.2, E88.0 Clinical summary This genetic test evaluates the F12 gene for mutations associated with Factor XII deficiency and Hereditary Angioedema type III.

Category overview

Genetic: overview

Unlocking the blueprint of your DNA provides profound, proactive insights into your family’s future and personal health risks. Integrated within our advanced Biochemistry and molecular services, specialized Genetic testing evaluates inherited traits, metabolic predispositions, and carrier statuses. Utilizing cutting-edge diagnostic technology, comprehensive genetic screening offers the vital clarity needed to safely guide tailored medical strategies and family planning. As an undisputed leader in innovation among diagnostic labs in Dubai and the UAE, DNA Labs guarantees the highest standards of strict patient confidentiality, unparalleled diagnostic precision, and rapid reporting. Empower your health decisions with certainty—book your genetic testing in UAE, coordinate a secure sample collection, or connect with our specialized genetics team today.

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