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.

Tests in this category

2,789

Listed price range

-1.00–50,000.00 AED

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Genetics test prices

Showing 2506–2520 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5090 TBXAS1 Gene Ghosal Hematodiaphyseal Syndrome Genetic Test This test analyzes the TBXAS1 gene to detect pathogenic variants associated with Ghosal Hematodiaphyseal Syndrome.	Whole Blood (EDTA) or Dried Blood Spot (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 TBXAS1 gene"] Parameters [] Preparation ["No fasting required", "Detailed family history required during pre-genetic counseling"] Indications ["Suspected Ghosal Hematodiaphyseal Syndrome", "Family history of GHDD", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 91898-8 ICD-10: Q78.8 Clinical summary This test analyzes the TBXAS1 gene to detect pathogenic variants associated with Ghosal Hematodiaphyseal Syndrome.
TEST-4337 TCAP Gene Cardiomyopathy, Dilated Type 1N Genetic Test This genetic test identifies pathogenic variants in the TCAP gene associated with Dilated Cardiomyopathy Type 1N.	Peripheral whole blood (2 mL EDTA) or saliva (Oragene kit)	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 TCAP gene", "Single nucleotide variants", "Small insertions and deletions", "Larger structural rearrangements"] Parameters [] Preparation [] Indications ["Diagnosis of Dilated Cardiomyopathy Type 1N", "Familial cascade screening for CMD1N", "Personalised clinical management"] Measurement technique Confirm with laboratory Codes LOINC: 51958-7 ICD-10: I42.0 Clinical summary This genetic test identifies pathogenic variants in the TCAP gene associated with Dilated Cardiomyopathy Type 1N.
TEST-4731 TCAP Gene Limb-Girdle Muscular Dystrophy Type 2G (LGMDR2) Genetic Test This genetic test analyzes the TCAP gene to identify pathogenic variants associated with Limb-Girdle Muscular Dystrophy Type 2G (LGMDR2).	Peripheral Whole Blood, Dried Blood Spot, or DNA Sample	3 to 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TCAP gene coding region", "Single nucleotide variants (SNVs)", "Small insertions and deletions (indels)"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any recent blood transfusions"] Indications ["Clinical suspicion of Limb-Girdle Muscular Dystrophy Type 2G (LGMDR2)", "Family history of LGMDR2", "Carrier screening for relatives"] Measurement technique Confirm with laboratory Codes LOINC: 81247-5 ICD-10: G71.0 Clinical summary This genetic test analyzes the TCAP gene to identify pathogenic variants associated with Limb-Girdle Muscular Dystrophy Type 2G (LGMDR2).
TEST-2911 TCF12 Gene Craniosynostosis Type 3 Genetic Test This test identifies pathogenic variants within the TCF12 gene associated with craniosynostosis type 3.	Peripheral Whole Blood	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 TCF12 gene", "Single nucleotide variants", "Small insertions and deletions"] Parameters [] Preparation ["No fasting required.", "No medication adjustments required."] Indications ["Diagnosis of craniosynostosis type 3", "Recurrence risk counselling", "Surgical planning"] Measurement technique Confirm with laboratory Codes LOINC: 94222-8 ICD-10: Q75.0 Clinical summary This test identifies pathogenic variants within the TCF12 gene associated with craniosynostosis type 3.
TEST-2427 TCF4 Gene Pitt-Hopkins Syndrome Genetic Test This genetic test analyzes the TCF4 gene to identify mutations associated with Pitt-Hopkins Syndrome.	Whole Blood (EDTA), Extracted DNA, or FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single nucleotide variants in TCF4 gene", "Small indels in TCF4 gene", "Copy number variants in TCF4 gene"] Parameters [] Preparation [] Indications ["Suspected Pitt-Hopkins Syndrome", "Evaluation of severe intellectual disability", "Dysmorphology evaluations"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: Q87.0 Clinical summary This genetic test analyzes the TCF4 gene to identify mutations associated with Pitt-Hopkins Syndrome.
TEST-4698 TCIRG1 Gene Osteopetrosis Autosomal Recessive Type 1 Genetic Test This diagnostic test evaluates the TCIRG1 gene for pathogenic variants associated with autosomal recessive osteopetrosis type 1.	Peripheral whole blood (EDTA tube)	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 TCIRG1 gene"] Parameters [] Preparation [] Indications ["Confirmation of clinical suspicion of ARO1", "Carrier screening", "Prenatal diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 88857-4 ICD-10: Q78.2 Clinical summary This diagnostic test evaluates the TCIRG1 gene for pathogenic variants associated with autosomal recessive osteopetrosis type 1.
TEST-5839 TCN2 Gene (Transcobalamin II Deficiency) Genetic Test This genetic test identifies pathogenic variants in the TCN2 gene, which are responsible for Transcobalamin II deficiency.	Whole Blood (EDTA), Extracted DNA, or Dried Blood Spot (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 TCN2 gene", "Vitamin B₁₂ transport function"] Parameters [] Preparation [] Indications ["Suspected Transcobalamin II deficiency", "Positive family history", "Clinical presentation consistent with B₁₂ deficiency"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: E53.8 Clinical summary This genetic test identifies pathogenic variants in the TCN2 gene, which are responsible for Transcobalamin II deficiency.
TEST-2232 TCOF1 Gene (Treacher Collins Syndrome Type 1) Genetic Test This genetic test evaluates the TCOF1 gene for pathogenic variants associated with Treacher Collins syndrome type 1.	Peripheral blood 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 TCOF1 gene", "Entire coding region and splice sites"] Parameters [] Preparation ["No fasting required", "Prior genetic counseling session to document family pedigree is mandatory", "Pre-clinical history documentation"] Indications ["Confirmation of Treacher Collins syndrome type 1 diagnosis", "Guiding surgical planning", "Recurrence risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 21647-4 ICD-10: Q75.4 Clinical summary This genetic test evaluates the TCOF1 gene for pathogenic variants associated with Treacher Collins syndrome type 1.
TEST-4650 TCTN1 Gene Joubert Syndrome Type 13 Genetic Test This diagnostic test evaluates the TCTN1 gene for pathogenic variants associated with Joubert syndrome type 13.	Peripheral whole blood	3–4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in TCTN1 gene", "Single nucleotide variants (SNVs)", "Small indels"] Parameters [] Preparation ["No specific fasting required", "No medication adjustments needed"] Indications ["Suspected Joubert syndrome type 13", "Confirmation of clinical diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 21636-9 ICD-10: Q04.3 Clinical summary This diagnostic test evaluates the TCTN1 gene for pathogenic variants associated with Joubert syndrome type 13.
TEST-3642 TCTN2 Gene (Meckel Syndrome Type 8) Genetic Test This genetic test evaluates the TCTN2 gene for pathogenic variants associated with Meckel syndrome type 8.	Peripheral Blood (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 TCTN2 gene", "SNVs, indels, CNVs"] Parameters [] Preparation [] Indications ["Suspected Meckel syndrome type 8", "Family history of Meckel syndrome type 8", "Prenatal diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q87.8 Clinical summary This genetic test evaluates the TCTN2 gene for pathogenic variants associated with Meckel syndrome type 8.
TEST-4591 TCTN2 Gene Joubert Syndrome Type 24 Genetic Test This test identifies pathogenic variants within the TCTN2 gene, which are causative for Joubert syndrome type 24.	Peripheral whole blood (3–5 mL in EDTA tube)	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 TCTN2 gene", "Full gene coverage including intronic regions"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication"] Indications ["Clinical suspicion of Joubert syndrome type 24", "Family history of Joubert syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 101391-0 ICD-10: Q04.3 Clinical summary This test identifies pathogenic variants within the TCTN2 gene, which are causative for Joubert syndrome type 24.
TEST-2477 TCTN3 Gene Sequencing for Orofaciodigital Syndrome Type 4 Test This test detects pathogenic variants in the TCTN3 gene associated with Orofaciodigital Syndrome Type 4.	Whole Blood or Buccal Swab	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 TCTN3 gene", "Single-nucleotide variants", "Small insertions", "Small deletions"] Parameters [] Preparation ["No special preparation required", "No fasting required"] Indications ["Clinical suspicion of Orofaciodigital Syndrome Type 4"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q87.0 Clinical summary This test detects pathogenic variants in the TCTN3 gene associated with Orofaciodigital Syndrome Type 4.
TEST-5906 TDP1 Gene (SCAN1) Spinocerebellar Ataxia with Axonal Neuropathy Genetic Test This genetic test evaluates the TDP1 gene for pathogenic variants associated with Spinocerebellar Ataxia with Axonal Neuropathy (SCAN1).	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 TDP1 gene", "DNA repair enzyme function"] Parameters [] Preparation ["No fasting required", "No medication adjustments required"] Indications ["Suspected diagnosis of SCAN1", "Family history of SCAN1", "Genetic counseling for at-risk family members"] Measurement technique Confirm with laboratory Codes LOINC: 77785-2 ICD-10: G11.1 Clinical summary This genetic test evaluates the TDP1 gene for pathogenic variants associated with Spinocerebellar Ataxia with Axonal Neuropathy (SCAN1).
TEST-5672 TECPR2 Gene SPG49 Genetic Test This test detects pathogenic variants in the TECPR2 gene to diagnose autosomal recessive spastic paraplegia type 49 (SPG49).	Whole blood, extracted DNA, or dried blood spot (FTA card)	3–4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TECPR2 gene", "Copy-number variants (CNVs) in the TECPR2 gene"] Parameters [] Preparation ["Provide comprehensive neurological history", "Mandatory pre-test genetic counseling", "Signed informed consent"] Indications ["Diagnosis of suspected autosomal recessive spastic paraplegia type 49 (SPG49)", "Family counseling for TECPR2-associated conditions", "Recurrence risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 69548-6 ICD-10: G11.4, Z13.7, Z14.8 Clinical summary This test detects pathogenic variants in the TECPR2 gene to diagnose autosomal recessive spastic paraplegia type 49 (SPG49).
TEST-4855 TECR Gene Sequencing (Intellectual Disability, Autosomal Recessive Type 14) Test This test identifies pathogenic variants in the TECR gene associated with autosomal recessive intellectual disability type 14.	Whole blood, extracted DNA, 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 TECR gene", "Coverage of coding regions"] Parameters [] Preparation ["Provide detailed clinical history", "Provide developmental milestones", "Provide family pedigree", "Genetic counselling session required"] Indications ["Suspected autosomal recessive intellectual disability type 14", "Family history of neurodevelopmental disorders"] Measurement technique Confirm with laboratory Codes LOINC: 96669-4 ICD-10: F79, Q02, Z15.89 Clinical summary This test identifies pathogenic variants in the TECR gene associated with autosomal recessive intellectual disability type 14.

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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