Albinism Genetic tests in Dubai & UAE

Compare available Albinism 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

Listed price range

2,800.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Albinism Genetic test prices

Showing 1–3 of 3 matching tests.

Albinism Genetic diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5428 SLC24A5 Gene Oculocutaneous Albinism Nonsyndromic Genetic Test This test evaluates the SLC24A5 gene for mutations associated with Oculocutaneous Albinism Type 6 (OCA6), a condition characterized by reduced pigmentation.	Peripheral Whole Blood, EDTA Tube (3-5 mL)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SLC24A5 gene sequence", "Mutation types (SNVs, indels, CNVs)"] Parameters [] Preparation ["No fasting required", "Continue all medications unless advised otherwise by your doctor", "Attend pre-test genetic counselling session"] Indications ["Suspected Oculocutaneous Albinism Type 6", "Family history of OCA6", "Individuals with pigment dilution, nystagmus, or photophobia"] Measurement technique Confirm with laboratory Codes LOINC: 94852-4 ICD-10: E70.31 Clinical summary This test evaluates the SLC24A5 gene for mutations associated with Oculocutaneous Albinism Type 6 (OCA6), a condition characterized by reduced pigmentation.
TEST-3466 SLC24A5 Gene Oculocutaneous Nonsyndromic Albinism Genetic Test This diagnostic assay utilizes Illumina Next-Generation Sequencing to detect pathogenic variants, including SNVs, indels, and CNVs, within the SLC24A5 gene.	Whole Blood (EDTA), Extracted DNA, or FTA Card Blood Spot	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)", "Small Insertions/Deletions (indels)", "Copy Number Variants (CNVs)"] Parameters [] Preparation ["Fasting is not required", "Continue all current medications unless instructed otherwise by your physician"] Indications ["Clinical features suggestive of oculocutaneous albinism", "Family history suggestive of autosomal recessive inheritance"] Measurement technique Confirm with laboratory Codes LOINC: 94494-2 ICD-10: E70.33 Clinical summary This diagnostic assay utilizes Illumina Next-Generation Sequencing to detect pathogenic variants, including SNVs, indels, and CNVs, within the SLC24A5 gene.
TEST-5425 TYR Gene (Oculocutaneous Albinism Type 1B) Genetic Test This genetic test analyzes the TYR gene to identify mutations causing Oculocutaneous Albinism Type 1B (OCA1B). It provides a definitive molecular diagnosis for this specific type o...	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 ["Mutations in the TYR gene", "Single-nucleotide variants (SNVs)", "Small indels"] Parameters [{"name": "Gene Coverage", "reference_range": "Full TYR coding region + 20 bp intronic flanks"}, {"name": "Sensitivity", "reference_range": ">99.9% for single‑nucleotide variants & small indels"}] Preparation ["No fasting required", "Mandatory pre-test genetic counselling session", "Clinical history form submission prior to collection"] Indications ["Suspected diagnosis of Oculocutaneous Albinism Type 1B (OCA1B)", "Differentiation from other hypopigmentation disorders", "Family planning and prenatal diagnosis", "Genetic counselling"] Measurement technique Confirm with laboratory Codes LOINC: 64652-5 ICD-10: E70.319 Clinical summary This genetic test analyzes the TYR gene to identify mutations causing Oculocutaneous Albinism Type 1B (OCA1B). It provides a definitive molecular diagnosis for this specific type of albinism.

Category overview

Albinism Genetic: overview

Understanding the exact hereditary pathways of albinism in your family empowers you to make proactive, highly informed decisions for long-term health and reproductive planning. Representing a critical component of our Molecular Genetics services, comprehensive Albinism Genetic screening provides an in-depth evaluation of the multiple genes responsible for pigment production. Utilizing advanced diagnostic technology, this targeted genomic testing delivers the precise clarity required to assess carrier status and inheritance risks, safely guiding specialized medical oversight and reproductive counseling. Highly regarded among top diagnostic labs in Dubai and the UAE, DNA Labs guarantees strict patient confidentiality, unparalleled diagnostic precision, and remarkably fast reporting. Empower your family's customized healthcare journey—book your albinism genetic testing in UAE, coordinate a comfortable home sample collection, or connect with our specialized genetic counselors today.

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.