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Diagnostic options ยท UAE

Hereditary Cancer Genetics tests in Dubai & UAE

Compare available Hereditary Cancer 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

4

Listed price range

2,800.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

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Hereditary Cancer Genetics test prices

Showing 1โ€“4 of 4 matching tests.

Hereditary Cancer Genetics diagnostic tests, details, and listed prices
Test and description Specimen Typical duration Price Options
TEST-5325
EXT1 Gene (Familial Chondrosarcoma) Genetic Test

This genetic test evaluates the EXT1 gene for pathogenic variants associated with hereditary multiple exostoses and increased chondrosarcoma risk.

Whole Blood, Extracted DNA, or One Drop Blood on FTA Card 3โ€“4 Weeks 2,800.00 AED
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View test specifications and preparation
What it measures
["Pathogenic variants in the EXT1 gene", "Copy number variations (CNVs) in the EXT1 gene"]
Parameters
[{"name": "Analytical Sensitivity", "reference_range": ">99.9%"}, {"name": "Coverage", "reference_range": "100% of coding regions ยฑ10 bp"}]
Preparation
["No fasting required", "No specific medication or diet restrictions"]
Indications
["Diagnosis of Hereditary Multiple Exostoses (HME)", "Assessment of chondrosarcoma risk in individuals with HME", "Genetic counseling for families with HME or chondrosarcoma", "Pre-implantation genetic diagnosis (PGD) or prenatal diagnosis"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 88373-9 ICD-10: Q78.6, C41.9, Z15.09
Clinical summary
This genetic test evaluates the EXT1 gene for pathogenic variants associated with hereditary multiple exostoses and increased chondrosarcoma risk.
TEST-2001
MSH2 Gene Mismatch Repair Cancer Syndrome Genetic Test

This genetic test evaluates the MSH2 gene for mutations associated with Lynch syndrome, a hereditary cancer predisposition.

Peripheral whole blood or FTA card 3โ€“4 Weeks 2,800.00 AED
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View test specifications and preparation
What it measures
["MSH2 gene mutations (SNVs, indels, CNVs)", "Germline genetic variations"]
Parameters
[{"name": "MSH2 Gene Analysis", "reference_range": "No pathogenic variants detected"}]
Preparation
["Do not discontinue prescribed medications without consulting your doctor.", "A pre-test genetic counselling session is mandatory."]
Indications
["Individuals with a personal or family history of Lynch-associated cancers", "Cascade testing for family members of individuals with known MSH2 mutations", "Diagnosis of Lynch syndrome"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 45068-8 ICD-10: Z15.09
Clinical summary
This genetic test evaluates the MSH2 gene for mutations associated with Lynch syndrome, a hereditary cancer predisposition.
TEST-2015
POT1 Gene Melanoma Susceptibility Test (Familial Type 10)

This test evaluates the POT1 gene for germline mutations associated with an increased risk of hereditary cutaneous malignant melanoma.

Whole Blood (EDTA) or Dried Blood Spots (FTA Card) 3โ€“4 weeks 2,800.00 AED
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View test specifications and preparation
What it measures
["Germline mutations in the POT1 gene", "Pathogenic variants associated with melanoma risk"]
Parameters
[]
Preparation
["No special fasting required", "Genetic counselling session required before sample collection"]
Indications
["Individuals with a strong family history of melanoma", "Patients with multiple primary melanomas", "Individuals diagnosed with melanoma before age 40"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 93931-7 ICD-10: Z15.09
Clinical summary
This test evaluates the POT1 gene for germline mutations associated with an increased risk of hereditary cutaneous malignant melanoma.
TEST-1945
SDHD Gene (Paraganglioma & GIST) Genetic Test

This genetic test identifies germline mutations in the SDHD gene associated with hereditary paraganglioma-pheochromocytoma syndrome and GIST.

Peripheral whole blood (EDTA), DNA FTA card 3โ€“4 weeks 2,800.00 AED
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View test specifications and preparation
What it measures
["SDHD gene mutations", "Germline variants"]
Parameters
[]
Preparation
["No specific fasting required", "Inform phlebotomist of any medications"]
Indications
["Suspected hereditary paraganglioma-pheochromocytoma syndrome", "Suspected hereditary GIST", "Family history of paraganglioma, pheochromocytoma, or GIST"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 56143-8 ICD-10: C75.5, D44.6
Clinical summary
This genetic test identifies germline mutations in the SDHD gene associated with hereditary paraganglioma-pheochromocytoma syndrome and GIST.

Category overview

Hereditary Cancer Genetics: overview

A family history of cancer can weigh heavily on your mind, but uncovering your specific molecular blueprint brings profound peace of mind and actionable clarity. Within our Molecular Diagnostics division, our Hereditary Cancer Genetics testing utilizes advanced DNA sequencing to safely map inherited vulnerabilities linked to various malignancies. Rather than providing an absolute clinical diagnosis, this precise hereditary cancer genetics data equips your oncologist with the vital insights needed for tailored, proactive medical guidance. Recognized among the most trusted diagnostic labs in Dubai and the UAE, DNA Labs UAE guarantees uncompromising patient privacy alongside exceptionally fast, accurate turnaround times. Prioritize your preventive health strategy today: explore our hereditary cancer genetics testing in the UAE below to book an appointment, schedule a convenient home sample collection, or consult our specialized team.

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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.