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 151–165 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5225 ANO5 Gene Miyoshi Muscular Dystrophy Type 3 Genetic Test This test detects pathogenic variants in the ANO5 gene to confirm Miyoshi muscular dystrophy type 3 and related ANO5‑associated myopathies.	Peripheral Whole Blood (5–10 mL in 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 ANO5 gene", "Single nucleotide variants", "Indels", "Copy number changes"] Parameters [] Preparation ["Joint consent from both parents or a legal guardian required for individuals under 18 years", "Reschedule if patient received a whole blood transfusion in the preceding 14 days"] Indications ["Individuals with progressive distal leg muscle weakness, calf atrophy, and highly elevated creatine kinase levels suggestive of Miyoshi myopathy", "At-risk family members seeking predictive or carrier testing", "Couples planning a family who wish to understand recurrence risk"] Measurement technique Confirm with laboratory Codes LOINC: 94051-0 ICD-10: G71.0 Clinical summary This test detects pathogenic variants in the ANO5 gene to confirm Miyoshi muscular dystrophy type 3 and related ANO5‑associated myopathies.
TEST-5043 ANTXR2 Gene Hyaline Fibromatosis Syndrome Genetic Test This genetic test evaluates the ANTXR2 gene for mutations causing hyaline fibromatosis syndrome.	Peripheral Whole Blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ANTXR2 gene mutations", "Copy number variations in ANTXR2"] Parameters [] Preparation ["No special preparation required", "Prior genetic counseling is recommended"] Indications ["Suspicion of hyaline fibromatosis syndrome", "Family history of hyaline fibromatosis syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 98059-9 ICD-10: Q82.8, M79.89, Z13.79 Clinical summary This genetic test evaluates the ANTXR2 gene for mutations causing hyaline fibromatosis syndrome.
TEST-4786 AP1S1 Gene MEDNIK Syndrome Genetic Test This test detects pathogenic variants in the AP1S1 gene associated with MEDNIK syndrome.	Whole blood (EDTA tube) or buccal swab	3–4 Weeks (Expedited)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["AP1S1 gene variants", "Disease-causing mutations"] Parameters [{"name": "Diagnostic Sensitivity (SNVs & indels)", "reference_range": ">99.5%"}, {"name": "Diagnostic Sensitivity (CNVs)", "reference_range": "~95%"}, {"name": "Methodology", "reference_range": "NGS (Targeted Gene Sequencing) with deletion/duplication analysis, Sanger confirmation"}] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting your doctor"] Indications ["Suspected MEDNIK syndrome", "Patients with hallmark signs of the syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 78126-8 ICD-10: Q87.8 Clinical summary This test detects pathogenic variants in the AP1S1 gene associated with MEDNIK syndrome.
TEST-4934 AP1S2 Gene X-Linked Intellectual Disability (XLID) Type 59 Genetic Test This test diagnoses X-linked intellectual disability type 59 by sequencing the AP1S2 gene.	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 DNA variants in the AP1S2 gene", "Single nucleotide variants", "Small insertions/deletions", "Copy number variants"] Parameters [] Preparation ["No fasting required", "Pre-test genetic counselling is mandatory"] Indications ["Suspected X-linked intellectual disability type 59", "Family history of XLID type 59"] Measurement technique Confirm with laboratory Codes LOINC: 92878-5 ICD-10: F70, Q87.8 Clinical summary This test diagnoses X-linked intellectual disability type 59 by sequencing the AP1S2 gene.
TEST-3662 AP3B1 Gene Hermansky-Pudlak Syndrome Type 2 Genetic Test This genetic test identifies pathogenic variants in the AP3B1 gene associated with Hermansky-Pudlak syndrome type 2.	Peripheral whole blood 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 AP3B1 gene", "Single nucleotide variants (SNVs)", "Insertions/deletions (indels)", "Copy number variants (CNVs)"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Definitive molecular diagnosis of Hermansky-Pudlak syndrome type 2", "Carrier screening", "Family planning in at-risk individuals"] Measurement technique Confirm with laboratory Codes LOINC: 81247-7 ICD-10: E70.320, D69.1, H55.8 Clinical summary This genetic test identifies pathogenic variants in the AP3B1 gene associated with Hermansky-Pudlak syndrome type 2.
TEST-5674 AP4E1 Gene SPG51 Genetic Test This test screens for pathogenic variants in the AP4E1 gene associated with hereditary spastic paraplegia type 51 (SPG51).	Peripheral Whole Blood (EDTA) or Saliva	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 AP4E1 gene", "Full exon and splice-site analysis"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any recent bone marrow transplant"] Indications ["Suspected hereditary spastic paraplegia type 51 (SPG51)", "Family history of SPG51"] Measurement technique Confirm with laboratory Codes LOINC: 94486-1 ICD-10: G11.4 Clinical summary This test screens for pathogenic variants in the AP4E1 gene associated with hereditary spastic paraplegia type 51 (SPG51).
TEST-2566 AP4M1 Gene Microcephaly Genetic Test This test identifies pathogenic variants in the AP4M1 gene associated with autosomal recessive microcephaly.	Peripheral Blood (FTA Card or Venous Draw)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["AP4M1 gene coding region", "AP4M1 gene conserved splice sites"] Parameters [] Preparation [] Indications ["Suspected AP4M1-related microcephaly", "Family history of autosomal recessive microcephaly"] Measurement technique Confirm with laboratory Codes LOINC: 94233-2 ICD-10: Q02 Clinical summary This test identifies pathogenic variants in the AP4M1 gene associated with autosomal recessive microcephaly.
TEST-5773 AP4M1 Gene SPG50 Genetic Test This test identifies mutations in the AP4M1 gene associated with Hereditary Spastic Paraplegia type 50 (SPG50).	Peripheral whole blood (3–5 mL EDTA), dried blood spot on FTA card, or previously extracted genomic DNA	3 – 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["AP4M1 gene sequence variants", "Mutations associated with SPG50"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications"] Indications ["Individuals with clinical features of hereditary spastic paraplegia", "Individuals with a confirmed family history of SPG50", "Couples planning a family where one partner carries a known AP4M1 mutation"] Measurement technique Confirm with laboratory Codes LOINC: 94482-6 ICD-10: G11.4 Clinical summary This test identifies mutations in the AP4M1 gene associated with Hereditary Spastic Paraplegia type 50 (SPG50).
TEST-5777 AP4S1 Gene (SPG52) Genetic Test This test analyzes the AP4S1 gene to detect pathogenic variants associated with Hereditary Spastic Paraplegia Type 52 (SPG52).	Whole Blood (EDTA), Extracted DNA, 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 ["Pathogenic variants in the AP4S1 gene coding region and splice-site junctions", "Presence or absence of mutations causing SPG52"] Parameters [] Preparation ["Clinical history review", "Genetic counseling session", "Routine blood draw (no fasting needed)"] Indications ["Clinical suspicion of Hereditary Spastic Paraplegia Type 52 (SPG52)", "Family history of SPG52", "Neurological symptoms consistent with SPG52"] Measurement technique Confirm with laboratory Codes LOINC: 93437-5 ICD-10: G11.4, Z13.71 Clinical summary This test analyzes the AP4S1 gene to detect pathogenic variants associated with Hereditary Spastic Paraplegia Type 52 (SPG52).
TEST-5770 AP5Z1 Gene SPG48 Genetic Test This test sequences the AP5Z1 gene using NGS to detect mutations causing hereditary spastic paraplegia type 48 (SPG48). It identifies single-nucleotide variants, small insertions/d...	Peripheral Whole Blood (3–5 mL EDTA) or FTA Card Finger-Prick	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["AP5Z1 gene sequence", "Single-nucleotide variants", "Small insertions/deletions", "Copy-number variants"] Parameters [] Preparation ["No fasting required", "No special preparation required"] Indications ["Clinical suspicion of SPG48", "Family history of hereditary spastic paraplegia", "Carrier screening for SPG48"] Measurement technique Confirm with laboratory Codes LOINC: 82675-3 ICD-10: G11.4, Z13.7 Clinical summary This test sequences the AP5Z1 gene using NGS to detect mutations causing hereditary spastic paraplegia type 48 (SPG48). It identifies single-nucleotide variants, small insertions/deletions, and copy-number variants.
TEST-2093 APC Gene (Familial Adenomatous Polyposis Coli) Genetic Test This genetic test detects pathogenic variants in the APC gene associated with Familial Adenomatous Polyposis (FAP).	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 ["Pathogenic variants in the APC gene", "Point mutations", "Small insertions/deletions", "Large rearrangements (copy number variants)"] Parameters [] Preparation ["No fasting required", "No medication changes required"] Indications ["Diagnosis of Familial Adenomatous Polyposis (FAP)", "Risk assessment for individuals with a family history of FAP", "Pre-symptomatic testing in at-risk family members"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: D12.6, Z15.04 Clinical summary This genetic test detects pathogenic variants in the APC gene associated with Familial Adenomatous Polyposis (FAP).
TEST-2076 APC Gene Desmoid Disease Hereditary Genetic Test This test identifies pathogenic variants in the APC gene associated with hereditary desmoid disease and familial adenomatous polyposis (FAP).	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 APC gene", "Hereditary predisposition to desmoid disease and FAP"] Parameters [] Preparation ["No fasting required", "Stay well-hydrated", "Bring Emirates ID and previous genetic reports"] Indications ["Personal or family history of desmoid tumours", "Personal or family history of FAP"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Z15.09, D48.1, M72.6 Clinical summary This test identifies pathogenic variants in the APC gene associated with hereditary desmoid disease and familial adenomatous polyposis (FAP).
TEST-5415 APC2-Related Neurodevelopmental Disorder Genetic Test This test detects pathogenic variants in the APC2 gene associated with neurodevelopmental delays and intellectual disability.	Peripheral whole blood (EDTA) or Dried Blood Spot (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 APC2 gene", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Splice-site alterations"] Parameters [] Preparation [] Indications ["Individuals with clinical features suggestive of APC2-related neurodevelopmental disorder", "Family history of APC2-related disorders", "Diagnostic confirmation"] Measurement technique Confirm with laboratory Codes LOINC: 74092-0 ICD-10: F84.9 Clinical summary This test detects pathogenic variants in the APC2 gene associated with neurodevelopmental delays and intellectual disability.
TEST-6132 APOA1 Gene Hypoalphalipoproteinemia Genetic Test This genetic test identifies pathogenic variants in the APOA1 gene associated with primary hypoalphalipoproteinemia.	Peripheral Whole Blood (EDTA), Extracted DNA, 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 ["APOA1 gene sequence", "Pathogenic variants (SNVs, indels, CNVs)"] Parameters [] Preparation ["No fasting required"] Indications ["Diagnosis of primary hypoalphalipoproteinemia", "Family screening for APOA1 variants", "Personalized cardiovascular risk management"] Measurement technique Confirm with laboratory Codes LOINC: 93977-2 ICD-10: E78.6 Clinical summary This genetic test identifies pathogenic variants in the APOA1 gene associated with primary hypoalphalipoproteinemia.
TEST-6104 APOA2 Gene Apolipoprotein A‑II Deficiency Genetic Test This genetic test identifies pathogenic variants in the APOA2 gene associated with Apolipoprotein A‑II deficiency.	Peripheral whole blood (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 APOA2 gene", "Coding exons", "Splice sites", "Copy number variations (CNVs)"] Parameters [] Preparation ["Genetic counselling session mandatory before sample collection", "Draw pedigree chart of affected family members"] Indications ["Diagnosis of Apolipoprotein A‑II deficiency", "Assessment of inherited lipid disorder risk"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: E78.8 Clinical summary This genetic test identifies pathogenic variants in the APOA2 gene associated with Apolipoprotein A‑II deficiency.

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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