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Biochemistry

Genetic Tests in Dubai & UAE

Investigations in this area, with the specimen type, turnaround time and listed price for each option — so you and your clinician can compare before you book.

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  • Home collection across the UAE
  • Confidential handling of results

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Genetic investigations

Showing 421–435 of 805 listed investigations.

TEST-3570 LOINC 21636-6

LHCGR Gene Mutation Analysis (NGS) for Male Precocious Puberty Test

This diagnostic test evaluates the LHCGR gene for activating mutations associated with familial male-limited precocious puberty (testotoxicosis).

Specimen
Peripheral blood or FTA card (dried blood spot)
Turnaround
3–4 Weeks
What it measures
["Activating mutations in the LHCGR gene", "Molecular confirmation of testotoxicosis"]

Listed price

2,800.00 AED

Details
TEST-3550 LOINC 92309-2

LHX3 Gene Pituitary Hormone Deficiency, Combined Type 3 Genetic Test

This genetic test identifies pathogenic variants in the LHX3 gene associated with combined pituitary hormone deficiency type 3 (CPHD3).

Specimen
Whole blood (EDTA), extracted DNA, or FTA card
Turnaround
3–4 weeks
What it measures
["Pathogenic variants in the LHX3 gene", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number alteration...

Listed price

2,800.00 AED

Details
TEST-3555 LOINC 94494-6

LIM2 Gene Cataract, Cortical Pulverulent, Late-Onset Genetic Test

This genetic test evaluates the LIM2 gene for pathogenic variants associated with late-onset cortical pulverulent cataract.

Specimen
Whole Blood (EDTA), Extracted DNA, or FTA Card Spot
Turnaround
3–4 Weeks
What it measures
["Pathogenic variants in the LIM2 gene"]

Listed price

2,800.00 AED

Details
TEST-5002 LOINC 92822-6

LIPH Gene Hypotrichosis Type 7 Genetic Test

This genetic test identifies pathogenic variants in the LIPH gene associated with autosomal recessive hypotrichosis type 7.

Specimen
Peripheral Whole Blood (EDTA) or Buccal Swab / Dried Blood Spot (FTA Card)
Turnaround
21–28 business days
What it measures
["LIPH gene sequence", "Pathogenic variants (SNVs, indels, splice-site aberrations)"]

Listed price

2,800.00 AED

Details
TEST-5986 LOINC 55233-1

LMBRD1 Gene Methylmalonic Aciduria CblF Type Genetic Test

This test identifies pathogenic variants in the LMBRD1 gene associated with Methylmalonic Aciduria CblF type, a rare inherited metabolic disorder.

Specimen
Whole Blood (EDTA), Extracted DNA, or Dried Blood Spot on FTA Card
Turnaround
3 to 4 Weeks
What it measures
["LMBRD1 gene variants", "Pathogenic mutations"]

Listed price

2,800.00 AED

Details
TEST-4978 LOINC 21636-6

LPAR6 Gene Hypotrichosis Type 8 Genetic Test

This genetic test identifies pathogenic variants in the LPAR6 gene associated with autosomal recessive hypotrichosis type 8.

Specimen
Peripheral Whole Blood (EDTA)
Turnaround
3–4 Weeks (21–28 Days)
What it measures
["Pathogenic variants in the LPAR6 gene", "Deletion/duplication analysis of the LPAR6 gene"]

Listed price

2,800.00 AED

Details
TEST-3378 LOINC 94499-8

LRRC8A Gene Agammaglobulinemia Type 5 (Autosomal Recessive) Genetic Test

This test evaluates the LRRC8A gene for mutations associated with autosomal recessive agammaglobulinemia type 5, a primary immunodeficiency.

Specimen
Peripheral Whole Blood (EDTA tube) or Extracted DNA
Turnaround
3–4 Weeks (Expedited Available)
What it measures
["LRRC8A gene sequence", "Causative mutations (point mutations, insertions/deletions, deep intronic variants)"]

Listed price

2,800.00 AED

Details
TEST-3678 LOINC 81247-9

LTBP2 Gene Glaucoma Primary Type 3D Genetic Test

This test evaluates the LTBP2 gene for mutations associated with primary congenital glaucoma.

Specimen
Peripheral whole blood – EDTA tube (3–5 ml)
Turnaround
3–4 weeks (21–28 calendar days)
What it measures
["Pathogenic mutations in the LTBP2 gene", "Single-nucleotide variants", "Insertions", "Deletions", "Copy-number variations"]

Listed price

2,800.00 AED

Details
TEST-6243 LOINC 21636-6

LYRM4 Gene Combined Oxidative Phosphorylation Deficiency Type 19 Genetic Test

This test identifies pathogenic variants in the LYRM4 gene associated with Combined Oxidative Phosphorylation Deficiency Type 19 (COXPD19).

Specimen
Peripheral whole blood (3–5 mL) or dried blood spot (FTA card)
Turnaround
3 to 4 weeks
What it measures
["Pathogenic variants in the LYRM4 gene", "Coverage of coding regions and splice junctions"]

Listed price

2,800.00 AED

Details
TEST-1404 LOINC 81321-5

Lysosomal Storage Disorder Gene Panel Test

This test identifies pathogenic genetic variants in genes associated with lysosomal storage diseases.

Specimen
Peripheral Blood (3–5 mL), Amniotic Fluid, or Chorionic Villi
Turnaround
4–6 weeks
What it measures
["Pathogenic variants in genes linked to lysosomal storage diseases", "Single-nucleotide variants", "Insertions", "Deletions", "Copy-number...

Listed price

4,800.00 AED

Details
TEST-5295 LOINC 94042-4

LYST Gene Chediak‑Higashi Syndrome Genetic Test

This genetic test evaluates the entire coding region of the LYST gene for variants associated with Chediak-Higashi syndrome.

Specimen
Whole Blood, Extracted DNA, or Dried Blood Spot (FTA card)
Turnaround
3 to 4 weeks
What it measures
["LYST gene variants", "Single nucleotide variants (SNVs)", "Insertions/deletions (indels)", "Copy number variations (CNVs)"]

Listed price

2,800.00 AED

Details
TEST-5326 LOINC 94227-5

MACF1 Gene Neurodevelopmental Disorder (MACF1‑Related) Genetic Test

This genetic test analyzes the entire MACF1 gene to detect pathogenic variants associated with neurodevelopmental disorders.

Specimen
Peripheral whole blood
Turnaround
3–4 weeks from sample receipt
What it measures
["Pathogenic variants in the MACF1 gene", "Full gene coverage including intronic and regulatory regions"]

Listed price

2,800.00 AED

Details
TEST-3535 LOINC 81265-5

MAF Gene Cataract (Pulverulent/Cerulean) with or without Microcornea Test

This genetic test identifies pathogenic variants within the MAF gene associated with congenital pulverulent or cerulean cataracts, with or without microcornea.

Specimen
Peripheral whole blood (EDTA) or FTA card
Turnaround
3–4 weeks from sample receipt
What it measures
["MAF gene pathogenic variants", "Copy Number Variants (CNVs) in MAF gene"]

Listed price

2,800.00 AED

Details
TEST-3967 LOINC 82375-8

MAOA Gene (Brunner Syndrome) Genetic Test

This test evaluates the MAOA gene for pathogenic variants associated with Brunner syndrome, characterized by impulsive aggression and intellectual disability.

Specimen
Whole Blood, Extracted DNA, or FTA Card
Turnaround
3–4 Weeks
What it measures
["Pathogenic variants in the MAOA gene", "Copy Number Variations (CNV) in the MAOA gene"]

Listed price

2,800.00 AED

Details

Clinical overview

About Genetic

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.

Before your appointment

Preparation & sample collection

Follow the instructions you are given

Fasting, timing and medicine restrictions differ between investigations. The instructions for your specific request are confirmed when you book.

Bring your identification

A valid photo ID is required at collection so that your sample is matched correctly to your record.

Tell us about medicines

Prescription medicines, supplements and recent procedures can affect how an investigation is scheduled or interpreted — please mention them.

Ask before collection

If anything about preparation is unclear, contact us before your appointment. Preparation errors can affect reporting times.

Patient information

Frequently asked questions

Practical answers about Genetic testing at DNA Labs UAE. This information is general and does not replace advice from your treating clinician.

How do I choose the right Genetic test?

The correct investigation depends on what your clinician is trying to establish. Review the specimen type and turnaround time below, then confirm the choice with your treating doctor before booking.

What specimen is required?

Specimen requirements are listed for each investigation. If a request involves more than one sample type, our team will confirm what is needed at the time of booking.

Do you offer home sample collection in Dubai and the UAE?

Yes. Home collection can be arranged across Dubai and the wider UAE. Availability and appointment windows vary by location, so please confirm when you book.

How long do results take?

Turnaround depends on the investigation and the method used. The expected reporting time is confirmed with you before collection.

Is there anything I need to do before sample collection?

Some investigations require fasting, a specific collection time, or avoiding certain medicines or activities. Preparation details are shared when you book — please follow them and ask if anything is unclear.

How will I receive my report?

Reports are issued as secure digital documents and can be shared with your referring clinician on request. Please review results with a qualified clinician who can interpret them in context.

About this clinical information

The information on this Genetic page describes laboratory investigations in general terms. It is written to help you understand what an investigation involves — it is not a diagnosis and it is not a substitute for advice from your treating clinician.

  • Investigation names, specimen types and listed prices are reviewed against laboratory records.
  • Preparation guidance is indicative — confirm test-specific instructions before collection.
  • Content is updated when investigations, methods or reporting formats change.
  • Results are released to the patient and, on request, shared with the referring clinician.

We're here to help

Need help choosing a Genetic test?

Tell us what your clinician has requested and we'll confirm availability, price, preparation and the most convenient collection option — including home collection in Dubai and across the UAE.

Call +971 54 548 8731
  • Home collection available across the UAE
  • Digital reports delivered securely
  • Confidential handling of every request

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