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 2446–2460 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-6259 SSR4 Gene X-Linked Congenital Disorder of Glycosylation (CDG) Genetic Test This genetic test analyzes the SSR4 gene to detect mutations causing X-linked congenital disorder of glycosylation (CDG type Iy). It identifies single nucleotide variants, insertio...	Peripheral Whole Blood (3 mL 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 ["SSR4 gene sequence", "Copy number variations (CNVs) in SSR4 gene"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions"] Indications ["Suspected X-linked congenital disorder of glycosylation (CDG type Iy)", "Individuals with clinical features suggestive of CDG Iy", "Family planning for families with a history of CDG Iy"] Measurement technique Confirm with laboratory Codes LOINC: 91247-1 ICD-10: E77.8 Clinical summary This genetic test analyzes the SSR4 gene to detect mutations causing X-linked congenital disorder of glycosylation (CDG type Iy). It identifies single nucleotide variants, insertions, deletions, and copy number changes.
TEST-4291 ST3GAL3 Gene (Early Infantile Epileptic Encephalopathy Type 15) Genetic Test This genetic test evaluates the ST3GAL3 gene for mutations associated with early infantile epileptic encephalopathy type 15 (EIEE15). It identifies variants like SNVs, indels, and...	Peripheral Whole Blood (EDTA) or Buccal Swab	21–28 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ST3GAL3 gene sequence", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variations (CNVs)", "Splice-site variants"] Parameters [] Preparation ["No fasting required", "No medication changes required", "Detailed clinical history, prior EEG reports, and neuroimaging results needed for pre-test counselling"] Indications ["Diagnosis of EIEE15", "Identification of ST3GAL3 gene mutations", "Guiding targeted therapeutic decisions", "Prognostic counselling", "Informed family planning"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: G40.4 Clinical summary This genetic test evaluates the ST3GAL3 gene for mutations associated with early infantile epileptic encephalopathy type 15 (EIEE15). It identifies variants like SNVs, indels, and CNVs.
TEST-4955 ST3GAL3 Gene (Mental Retardation, Autosomal Recessive Type 12) Genetic Test This genetic test identifies pathogenic variants in the ST3GAL3 gene associated with autosomal recessive intellectual disability type 12.	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 the ST3GAL3 gene", "Single-nucleotide variants", "Missense variants", "Nonsense variants", "Splice-site variants", "Small insertions/deletions (indels)"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions"] Indications ["Suspected autosomal recessive intellectual disability type 12", "Family history of intellectual disability"] Measurement technique Confirm with laboratory Codes LOINC: 82914-3 ICD-10: Q87.8 Clinical summary This genetic test identifies pathogenic variants in the ST3GAL3 gene associated with autosomal recessive intellectual disability type 12.
TEST-3761 ST3GAL5 Gene Amish Infantile Epilepsy Syndrome Genetic Test This test detects pathogenic variants in the ST3GAL5 gene, confirming a diagnosis of Amish Infantile Epilepsy Syndrome.	Whole Blood (EDTA), Extracted DNA, or FTA Card Dried Blood Spot	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ST3GAL5 gene pathogenic variants", "Full coding region and deep intronic boundaries"] Parameters [] Preparation ["Clinical history review", "Genetic counselling session", "Three-generation pedigree chart construction"] Indications ["Clinical suspicion of Amish Infantile Epilepsy Syndrome", "Early-onset epileptic encephalopathy", "Unexplained seizures in early infancy"] Measurement technique Confirm with laboratory Codes LOINC: 21666-9 ICD-10: G40.4 Clinical summary This test detects pathogenic variants in the ST3GAL5 gene, confirming a diagnosis of Amish Infantile Epilepsy Syndrome.
TEST-1908 STAG1 Gene Prostate Cancer Genetic Test This test evaluates the STAG1 gene for variants associated with an increased risk of hereditary prostate cancer.	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 ["STAG1 gene variants", "Pathogenic and likely pathogenic mutations"] Parameters [] Preparation [] Indications ["Individuals with a strong family history of prostate cancer", "Men diagnosed with prostate cancer at a young age", "Families with multiple cancers suggesting hereditary syndromes"] Measurement technique Confirm with laboratory Codes LOINC: 21620-6 ICD-10: Z80.43 Clinical summary This test evaluates the STAG1 gene for variants associated with an increased risk of hereditary prostate cancer.
TEST-3824 STAT5B Gene Sequencing (Growth Hormone Insensitivity with Immunodeficiency) Test This test identifies pathogenic variants within the STAT5B gene, which are associated with growth hormone insensitivity and severe immunodeficiency.	Whole Blood (Peripheral)	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 STAT5B gene", "Single-nucleotide variants", "Small insertions/deletions", "Splice-site alterations"] Parameters [] Preparation ["No fasting required", "No medication changes required", "Inform phlebotomist of recent blood transfusions or stem cell therapy"] Indications ["Suspected growth hormone insensitivity", "Combined immunodeficiency", "Recurrent or severe infections", "Failure to thrive"] Measurement technique Confirm with laboratory Codes LOINC: 55231-4 ICD-10: E34.3, D84.9 Clinical summary This test identifies pathogenic variants within the STAT5B gene, which are associated with growth hormone insensitivity and severe immunodeficiency.
TEST-2555 STIL Gene Autosomal Recessive Primary Microcephaly Type 7 (MCPH7) Genetic Test This test identifies pathogenic variants in the STIL gene associated with autosomal recessive primary microcephaly type 7 (MCPH7).	Whole Blood (EDTA) or FTA Card (Dried Blood Spot)	21–28 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["STIL gene coding exons", "STIL gene splice junctions", "Copy Number Variants (CNVs)"] Parameters [] Preparation ["Pre-test genetic counselling session is mandatory"] Indications ["Infants with congenital microcephaly", "Children with unexplained intellectual disability", "Siblings of a confirmed MCPH7 case"] Measurement technique Confirm with laboratory Codes LOINC: 79714-0 ICD-10: Q02, Z13.79, Z82.71 Clinical summary This test identifies pathogenic variants in the STIL gene associated with autosomal recessive primary microcephaly type 7 (MCPH7).
TEST-3189 STIM1 Gene (Stormorken Syndrome) Genetic Test This test evaluates the STIM1 gene for pathogenic variants associated with Stormorken syndrome, an autosomal dominant disorder.	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 ["STIM1 gene sequence", "Pathogenic variants"] Parameters [] Preparation [] Indications ["Suspected Stormorken syndrome", "Family history of Stormorken syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 61693-7 ICD-10: D69.1 Clinical summary This test evaluates the STIM1 gene for pathogenic variants associated with Stormorken syndrome, an autosomal dominant disorder.
TEST-4939 STIM1 Gene Immunodeficiency Type 10 Genetic Test This test analyzes the STIM1 gene for pathogenic variants associated with combined immunodeficiency type 10.	Peripheral whole blood, saliva, 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 ["STIM1 gene variants", "Pathogenic mutations"] Parameters [] Preparation [] Indications ["Suspected STIM1-related immunodeficiency type 10", "Combined immunodeficiency", "Immune dysfunction syndromes"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: D84.8 Clinical summary This test analyzes the STIM1 gene for pathogenic variants associated with combined immunodeficiency type 10.
TEST-5363 STIM1 Gene Myopathy, Tubular Aggregate, Type 1 Genetic Test This test identifies pathogenic variants in the STIM1 gene associated with tubular aggregate myopathy type 1.	Whole Blood (EDTA), Extracted DNA, or Dried Blood Spot on FTA Card	21 – 28 calendar days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["STIM1 gene sequence", "Pathogenic variants (SNVs, indels, CNVs)"] Parameters [] Preparation ["Pre-test genetic counselling is mandatory", "Avoid heparin-based anticoagulants"] Indications ["Suspected STIM1-related tubular aggregate myopathy", "Congenital neuromuscular disorder investigation", "Genetic counselling"] Measurement technique Confirm with laboratory Codes LOINC: 94233-3 ICD-10: G71.03 Clinical summary This test identifies pathogenic variants in the STIM1 gene associated with tubular aggregate myopathy type 1.
TEST-1941 STK11 Gene (Peutz-Jeghers Syndrome) Genetic Test This genetic test evaluates the STK11 gene for mutations associated with Peutz-Jeghers syndrome, a hereditary condition increasing cancer risk.	Peripheral Whole Blood	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["STK11 gene mutations (SNVs, indels, deletions, duplications)", "Germline genetic alterations"] Parameters [] Preparation ["Pre-test genetic counselling is mandatory", "No specific fasting required for blood sample"] Indications ["Diagnosis of Peutz-Jeghers syndrome", "Assessment of hereditary cancer risk", "Family screening for STK11 mutations"] Measurement technique Confirm with laboratory Codes LOINC: 85196-1 ICD-10: Q85.8 Clinical summary This genetic test evaluates the STK11 gene for mutations associated with Peutz-Jeghers syndrome, a hereditary condition increasing cancer risk.
TEST-495 STR Profiling Test This test analyzes specific DNA markers (Short Tandem Repeats) to create a unique genetic profile for identification or lineage determination.	Whole Blood or Buccal Swab	10 working days	1,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Short Tandem Repeat (STR) markers", "Genetic identity"] Parameters [] Preparation [] Indications ["Paternity testing", "Forensic investigations", "Inheritance disputes", "Advanced genetic research"] Measurement technique Confirm with laboratory Codes LOINC: 73778-8 ICD-10: Z04.8 Clinical summary This test analyzes specific DNA markers (Short Tandem Repeats) to create a unique genetic profile for identification or lineage determination.
TEST-2420 STRADA Gene Polyhydramnios, Megalencephaly, and Symptomatic Epilepsy Genetic Test This test evaluates the STRADA gene for pathogenic variants associated with Polyhydramnios, Megalencephaly, and Symptomatic Epilepsy (PMSE) syndrome.	Whole Blood (Peripheral)	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 STRADA gene"] Parameters [] Preparation ["No specific patient preparation required"] Indications ["Suspected PMSE syndrome", "Family history of PMSE syndrome", "Carrier screening for at-risk family members"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: Q87.8 Clinical summary This test evaluates the STRADA gene for pathogenic variants associated with Polyhydramnios, Megalencephaly, and Symptomatic Epilepsy (PMSE) syndrome.
TEST-5718 STRC Gene (Autosomal Recessive Deafness Type 16) Genetic Test This genetic test evaluates the STRC gene for pathogenic variants associated with autosomal recessive deafness type 16 (DFNB16).	Whole Blood or Dried Blood Spot (DBS)	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 STRC gene", "Single-nucleotide variants", "Copy number variations"] Parameters [] Preparation ["A mandatory pre-test genetic counselling session is required."] Indications ["Suspected autosomal recessive deafness type 16 (DFNB16)", "Family history of STRC-related hearing loss"] Measurement technique Confirm with laboratory Codes LOINC: 81319-1 ICD-10: H90.5 Clinical summary This genetic test evaluates the STRC gene for pathogenic variants associated with autosomal recessive deafness type 16 (DFNB16).
TEST-3465 STRC Gene Deafness and Male Infertility Genetic Test This genetic test evaluates the STRC gene for pathogenic variants associated with autosomal recessive non-syndromic hearing loss and male infertility.	Peripheral Whole Blood, Extracted DNA, or 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 STRC gene"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist about bleeding disorders or anticoagulant use"] Indications ["Autosomal recessive non-syndromic hearing loss", "Male infertility", "Family history of hearing loss or infertility"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: H90.5, N46.9 Clinical summary This genetic test evaluates the STRC gene for pathogenic variants associated with autosomal recessive non-syndromic hearing loss and male infertility.

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

Genetics test prices

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