Genetics
Molecular Genetics 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.
- Quality-controlled laboratory
- Home collection across the UAE
- Confidential handling of results
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Molecular Genetics investigations
All 18 investigations in this category are listed below.
| Test | What it measures | Specimen | Turnaround | Price | Book |
|---|---|---|---|---|---|
| COL10A1 Gene Metaphyseal Chondrodysplasia, Schmid Type Genetic Test TEST-4797 LOINC 101651-1 | This genetic test analyzes the COL10A1 gene to detect pathogenic variants associated with metaphyseal chondrodysplasia Schmid type. | Peripheral Whole Blood | 3–4 Weeks | 2,800.00 AED | Details |
| CYLD Gene (Multiple Familial Trichoepithelioma Type 1) Genetic Test TEST-1896 LOINC 93792-9 | This test evaluates the CYLD gene for pathogenic mutations associated with multiple familial trichoepithelioma type 1. | Whole Blood (Peripheral), Extracted DNA, or Dried Blood Spot (FTA Card) | 3 – 4 weeks | 2,800.00 AED | Details |
| DKC1 Gene Dyskeratosis Congenita, X-Linked Genetic Test TEST-5190 LOINC 21603-0 | This genetic test identifies pathogenic variants in the DKC1 gene associated with X-linked dyskeratosis congenita. | Peripheral whole blood (3–5 mL) in EDTA tube; Dried Blood Spot (FTA card) | 3–4 weeks | 2,800.00 AED | Details |
| GPR161 Gene Pituitary Stalk Interruption Syndrome (GPR161-Related) Genetic Test TEST-5871 LOINC 81247-9 | This genetic test analyzes the GPR161 gene to detect variants associated with pituitary stalk interruption syndrome. | Peripheral Whole Blood (3–5 mL in EDTA tube), Extracted DNA (≥1 µg), or Dried Blood Spot on FTA Card | 3–4 Weeks | 2,800.00 AED | Details |
| IDH1 Gene Genetic Test for Metaphyseal Chondromatosis with D-2-Hydroxyglutaric Aciduria TEST-4780 LOINC 92769-6 | This test evaluates the IDH1 gene for pathogenic variants associated with metaphyseal chondromatosis and D-2-hydroxyglutaric aciduria. | Peripheral Whole Blood (EDTA), Buccal Swab, or Pre-Extracted DNA | 3–4 Weeks | 2,800.00 AED | Details |
| KRT1 Gene Epidermolytic Hyperkeratosis (EHK) Genetic Test TEST-5101 LOINC 90356-4 | This genetic test identifies pathogenic mutations in the KRT1 gene, confirming a diagnosis of epidermolytic hyperkeratosis (EHK). | Whole Blood, FTA Card, Extracted DNA | 3 to 4 Weeks | 2,800.00 AED | Details |
| Mucopolysaccharidosis Type II (MPS II) IDS Gene Genetic Test TEST-5942 LOINC 82850-2 | This test analyzes the IDS gene to detect pathogenic variants associated with Mucopolysaccharidosis Type II (Hunter syndrome). It provides a definitiv... | Whole blood (EDTA), extracted DNA, or dried blood spot (FTA card) | 3-4 Weeks | 2,800.00 AED | Details |
| NDP Gene Norrie Disease Genetic Test TEST-5490 LOINC 51952-3 | This test identifies pathogenic mutations within the NDP gene, confirming a diagnosis of Norrie disease. | Whole Blood (Peripheral Venous Blood) | 3–4 Weeks | 2,800.00 AED | Details |
| OGDH Gene Alpha‑Ketoglutarate Dehydrogenase Deficiency Genetic Test TEST-5981 LOINC 79324-3 | This genetic test evaluates the OGDH gene for mutations associated with alpha-ketoglutarate dehydrogenase deficiency, an inborn error of metabolism. | Peripheral whole blood (EDTA) | 3 to 4 weeks from sample receipt | 2,800.00 AED | Details |
| SERPING1 Gene Hereditary Angioedema Genetic Test TEST-4072 LOINC 82753-8 | This test identifies pathogenic mutations within the SERPING1 gene, confirming a diagnosis of hereditary angioedema types I and II. | Peripheral whole blood (3–5 mL in EDTA tube) or extracted DNA | 3–4 Weeks | 2,800.00 AED | Details |
| SGCG Gene LGMD2C Genetic Test TEST-4817 LOINC 55233-1 | This test analyzes the SGCG gene to detect mutations associated with Limb-Girdle Muscular Dystrophy Type 2C (LGMD2C). It identifies various types of g... | Peripheral Whole Blood (EDTA) or Extracted DNA | 3–4 Weeks | 2,800.00 AED | Details |
| SLC22A12 Gene (Renal Hypouricemia Type 1) Genetic Test TEST-3693 LOINC 101299-0 | This genetic test identifies pathogenic variants in the SLC22A12 gene associated with renal hypouricemia type 1. | Whole blood (EDTA) or FTA card blood spot | 3 – 4 weeks | 2,800.00 AED | Details |
| SLC6A2 Gene Orthostatic Intolerance Genetic Test TEST-4018 LOINC 81321-4 | This test analyzes the SLC6A2 gene for variants associated with orthostatic intolerance and autonomic dysfunction. | Whole blood (EDTA tube) or buccal swab | 3–4 weeks | 2,800.00 AED | Details |
| SMAD4 Gene Myhre Syndrome Genetic Test TEST-2525 LOINC 21636-6 | This test analyzes the entire SMAD4 gene using Next-Generation Sequencing (NGS) to detect pathogenic variants associated with Myhre syndrome. | Peripheral Whole Blood (EDTA) or Derived DNA | 3 to 4 Weeks | 2,800.00 AED | Details |
| ST3GAL3 Gene (Early Infantile Epileptic Encephalopathy Type 15) Genetic Test TEST-4291 LOINC 21636-6 | This genetic test evaluates the ST3GAL3 gene for mutations associated with early infantile epileptic encephalopathy type 15 (EIEE15). It identifies va... | Peripheral Whole Blood (EDTA) or Buccal Swab | 21–28 Business Days | 2,800.00 AED | Details |
| TBX19 Gene Adrenocorticotropic Hormone Deficiency Genetic Test TEST-3935 LOINC 94083-0 | This genetic test identifies pathogenic variants in the TBX19 gene associated with congenital isolated ACTH deficiency. | Whole Blood or FTA Card | 3–4 Weeks | 2,800.00 AED | Details |
| WAC Gene Desanto-Shinawi Syndrome Genetic Test TEST-2883 LOINC 92822-6 | This genetic test analyzes the WAC gene for pathogenic variants associated with Desanto-Shinawi Syndrome. | Whole Blood (EDTA), Extracted DNA, or FTA Card | 3 to 4 Weeks | 2,800.00 AED | Details |
| WNT7A Gene Sequencing for Fibular Aplasia/Hypoplasia, Femoral Bowing & Polydactyly (NGS) Test TEST-2841 LOINC 21836-0 | This test identifies pathogenic variants in the WNT7A gene associated with fibular aplasia/hypoplasia, femoral bowing, and polydactyly. | Peripheral blood (or extracted DNA; FTA card accepted for infants) | 3–4 weeks | 2,800.00 AED | Details |
Clinical overview
About Molecular Genetics
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 Molecular Genetics testing at DNA Labs UAE. This information is general and does not replace advice from your treating clinician.
How do I choose the right Molecular Genetics 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 Molecular Genetics 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.
Medical disclaimer: This page is for general information and education only. It is not medical advice, diagnosis or treatment, and it does not replace a consultation with a qualified healthcare professional. Always seek the advice of your doctor or another qualified provider with any questions about a medical condition or before ordering a test.
We're here to help
Need help choosing a Molecular Genetics 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.
- Home collection available across the UAE
- Digital reports delivered securely
- Confidential handling of every request
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