Diagnostic options · UAE

Exome Sequencing tests in Dubai & UAE

Compare available Exome Sequencing 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

Listed price range

2,800.00–9,100.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Exome Sequencing test prices

Showing 1–12 of 12 matching tests.

Exome Sequencing diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-15 Featured Whole Exome Sequencing (Exome Max) Test This test evaluates the DNA sequence of protein-coding regions across the entire exome to identify genetic variants.	Peripheral Whole Blood (5ml)	4 weeks	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in ~20,000 protein-coding genes", "Pharmacogenomic markers", "Hereditary cancer syndromes", "Single-gene disorders"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any medications"] Indications ["Diagnosis of rare genetic disorders", "Hereditary cancer risk assessment", "Pharmacogenomic analysis", "Personalized preventive medicine"] Measurement technique Confirm with laboratory Codes LOINC: 62374-9 ICD-10: Z01.89 Clinical summary This test evaluates the DNA sequence of protein-coding regions across the entire exome to identify genetic variants.
TEST-1035 Clinical Exome Sequencing (NGS) Test This test analyzes the coding regions of over 9,300 genes to identify genetic variants associated with rare and undiagnosed diseases.	Peripheral whole blood (EDTA tube)	4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Protein-coding regions of genes", "Pathogenic variants"] Parameters [] Preparation ["Avoid recent blood transfusion ( Indications ["Patients with complex or undiagnosed syndromes", "Suspected rare genetic disorders", "Family history of genetic conditions"] Measurement technique Confirm with laboratory Codes LOINC: 94222-5 ICD-10: Z01.818, R69 Clinical summary This test analyzes the coding regions of over 9,300 genes to identify genetic variants associated with rare and undiagnosed diseases.
TEST-467 Clinical Exome Sequencing for Couples (Preconception Carrier Screening) Test This test analyzes the coding regions of over 20,000 genes in both partners to identify carrier status for autosomal recessive and X-linked disorders.	Peripheral whole blood (2× 8.5 mL EDTA tubes) or buccal swab per partner	14 business days	5,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Carrier status for autosomal recessive disorders", "Carrier status for X-linked disorders", "Genetic variants in coding regions of ~20,000 genes"] Parameters [] Preparation ["Inform our team of current medications prior to sample collection", "Do not discontinue prescribed medication without consulting your physician"] Indications ["Couples planning a family", "Couples with a history of genetic disorders", "Couples with consanguinity", "Couples seeking comprehensive carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 81210-9 ICD-10: Z31.440, Z31.430, Z13.79 Clinical summary This test analyzes the coding regions of over 20,000 genes in both partners to identify carrier status for autosomal recessive and X-linked disorders.
TEST-451 Clinical Exome Trio Sequencing Test This test identifies genetic variants in the coding regions of genes from a child and both parents to diagnose rare genetic disorders.	Peripheral Whole Blood (3–5 mL per participant in EDTA tubes) or Saliva (Oragene OG-500 kit)	21 Business Days	7,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Coding regions (exomes) of genes", "Pathogenic variants", "Variants of uncertain significance (VUS)"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any recent bone marrow or stem cell transplant"] Indications ["Diagnosis of rare genetic disorders", "Identification of pathogenic variants", "Family history of genetic conditions"] Measurement technique Confirm with laboratory Codes LOINC: 94041-0 ICD-10: Z13.71, Z13.79, R89.8 Clinical summary This test identifies genetic variants in the coding regions of genes from a child and both parents to diagnose rare genetic disorders.
TEST-248 Human Exome Sequencing (Twist Core Exome Panel) Test This test analyzes the protein-coding regions of the genome to identify genetic variants associated with hereditary diseases.	Whole Blood or Extracted DNA	5 Weeks	3,500.00 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)"] Parameters [{"name": "Target Enrichment", "reference_range": "Twist Bioscience Double-Stranded Capture Probes – Uniform Coverage, Minimal GC Bias"}, {"name": "Diagnostic Yield", "reference_range": "≥99.9% Sensitivity for SNVs/Indels; Superior CNV Detection"}, {"name": "ISO Accreditation", "reference_range": "ISO 9001:2015 Certified (INT/EGQ/2509DA/3139)"}] Preparation ["No fasting required", "No medication changes needed", "Inform team of recent blood transfusions or bone marrow transplants"] Indications ["Diagnosis of hereditary cancers", "Diagnosis of inborn errors of metabolism", "Diagnosis of neurodevelopmental disorders", "Diagnosis of rare genetic syndromes"] Measurement technique Confirm with laboratory Codes LOINC: 84473-7 ICD-10: Z13.71 Clinical summary This test analyzes the protein-coding regions of the genome to identify genetic variants associated with hereditary diseases.
TEST-286 Human Exome Sequencing & Analysis (Twist Human Core Exome) Test This test analyzes the protein-coding regions of DNA to identify genetic variants linked to inherited diseases, cancer risk, and autoimmune conditions.	Whole Blood (2–5 mL EDTA) or Extracted DNA (≥1 µg, A260/A280 1.8–2.0)	8 weeks from sample receipt	5,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Protein-coding DNA variants", "Clinically relevant genetic mutations"] Parameters [] Preparation ["No special preparation needed", "Continue all prescribed medications unless advised otherwise by your doctor"] Indications ["Diagnosis of suspected inherited genetic disorders", "Assessment of cancer predisposition", "Investigation of autoimmune disorders", "Identification of variants in protein-coding regions"] Measurement technique Confirm with laboratory Codes LOINC: 94547-8 ICD-10: Z13.71 Clinical summary This test analyzes the protein-coding regions of DNA to identify genetic variants linked to inherited diseases, cancer risk, and autoimmune conditions.
TEST-255 Human Exome Sequencing Test This test analyzes the exome, the protein-coding portion of the genome, to identify disease-causing genetic variants.	Whole blood (3 mL in EDTA tube) or Extracted DNA (3 µg)	5 weeks	4,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Protein-coding regions (exons)", "Pathogenic variants"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Diagnosis of suspected monogenic disorders", "Identification of variants in patients with complex or undiagnosed conditions", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 94114-5 ICD-10: Z13.71, Z13.89 Clinical summary This test analyzes the exome, the protein-coding portion of the genome, to identify disease-causing genetic variants.
TEST-462 NGS Whole Exome for Couple Test This test assesses the protein-coding regions of the genome in both partners to identify shared genetic variants associated with recessive and X-linked disorders.	Peripheral whole blood	3–4 weeks	6,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Protein-coding regions of the genome (exome)", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)"] Parameters [] Preparation [] Indications ["Couples planning pregnancy", "Family history of genetic disorders", "Consanguineous marriages", "Previous affected pregnancies"] Measurement technique Confirm with laboratory Codes LOINC: 101297-1 ICD-10: Z13.89 Clinical summary This test assesses the protein-coding regions of the genome in both partners to identify shared genetic variants associated with recessive and X-linked disorders.
TEST-344 Whole Exome + Mitochondrial Genome Sequencing Test This test evaluates the entire coding region of the genome (exome) and the complete mitochondrial genome to identify genetic variants associated with hereditary disorders, cancer p...	Whole Blood (Peripheral Blood)	3–4 weeks	6,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Nuclear Exome Variants", "Mitochondrial Genome Variants"] Parameters [] Preparation ["No fasting required", "Inform doctor about recent transfusions or bone marrow transplants"] Indications ["Complex or undiagnosed conditions", "Hereditary disorders", "Cancer predisposition", "Mitochondrial syndromes"] Measurement technique Confirm with laboratory Codes LOINC: 81237-6 ICD-10: Z01.5, R69 Clinical summary This test evaluates the entire coding region of the genome (exome) and the complete mitochondrial genome to identify genetic variants associated with hereditary disorders, cancer predisposition, and mitochondrial syndromes.
TEST-558 Whole Exome Sequencing (WES) Test This test analyzes the protein-coding regions (exome) of the genome to identify genetic variants associated with inherited diseases.	Peripheral whole blood	4 weeks	3,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in protein-coding genes", "Genetic mutations linked to Mendelian disorders"] Parameters [] Preparation ["No special preparation is needed"] Indications ["Diagnosis of suspected inherited conditions", "Identification of genetic causes for developmental delays", "Evaluation of rare diseases", "Oncogenomics"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Z01.818 Clinical summary This test analyzes the protein-coding regions (exome) of the genome to identify genetic variants associated with inherited diseases.
TEST-194 Whole Exome Sequencing (WES) with Variant Calling & Annotation Test This diagnostic test evaluates the protein-coding regions of the genome to identify genetic variants potentially causing inherited disorders.	Peripheral whole blood (EDTA) or extracted gDNA	28 calendar days	3,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Protein-coding gene variants", "Pathogenic and likely pathogenic variants"] Parameters [{"name": "Sequencing Depth", "reference_range": "≥100× mean coverage (Illumina platform)"}, {"name": "Variant Calling & Annotation", "reference_range": "GATK-based, ACMG/AMP 5-tier classification, Ensembl VEP"}] Preparation [] Indications ["Individuals with clinical suspicion of a monogenic disorder", "Undiagnosed syndromes", "Developmental delays", "Multiple congenital anomalies", "Inherited neurological disorders"] Measurement technique Confirm with laboratory Codes LOINC: 93927-4 ICD-10: Z01.81, Z01.89 Clinical summary This diagnostic test evaluates the protein-coding regions of the genome to identify genetic variants potentially causing inherited disorders.
TEST-2752 Whole Exome Sequencing Trio Test This test identifies genetic variants in the protein-coding regions of the genome for the proband and both parents to diagnose genetic disorders.	Whole blood (EDTA)	6 Weeks	9,100.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Protein-coding regions (exome) of ~20,000 genes", "Variant inheritance patterns", "De novo mutations", "Autosomal recessive disorders", "X-linked conditions"] Parameters [] Preparation ["No specific fasting required", "No specific medication or diet restrictions"] Indications ["Suspected genetic disorder with unknown cause", "Complex diagnostic odysseys", "Need to differentiate inherited vs. de novo mutations", "Assessment of carrier status in parents"] Measurement technique Confirm with laboratory Codes LOINC: 93882-7 ICD-10: Z13.79, Z84.81, Z15.89 Clinical summary This test identifies genetic variants in the protein-coding regions of the genome for the proband and both parents to diagnose genetic disorders.

Category overview

Exome Sequencing: overview

When evaluating complex, unexplained medical conditions, analyzing the protein-coding regions of your DNA provides the definitive clarity your family needs. Under our Molecular Diagnostics umbrella, our Exome Sequencing testing employs high-resolution genomic technology to safely detect subtle genetic variations across all your genes. Instead of providing an isolated clinical diagnosis, this expansive molecular data acts as an essential tool for your geneticist, shaping highly targeted, proactive medical guidance for complex diagnostic odysseys. Renowned across premier diagnostic labs in the UAE, DNA Labs UAE ensures absolute patient privacy and incredibly fast, accurate results. Gain actionable clarity for your health: discover our exome sequencing testing in the UAE below to book your test, arrange a convenient home collection, or contact our medical specialists.

Before booking

Use the test details as a conversation starter

The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.