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Uncover Genetic Risks with Hereditary Cancer Genetic Testing

Hereditary cancer genetic testing identifies inherited gene mutations that may increase your risk of developing certain cancers. This comprehensive panel analyzes multiple genes associated with hereditary cancers—such as breast, ovarian, colon, and pancreatic cancers—empowering you and your healthcare provider with proactive insights for early intervention and risk management.
Conditions Detected by Hereditary Cancer Screening
01
BRCA1 and BRCA2 gene mutations
02
Lynch Syndrome (Colon and Endometrial Cancer)
03
Li-Fraumeni Syndrome
04
Familial Melanoma, Pancreatic, and Gastric Cancers
Empower Your Preventive Strategy

Personal Risk Awareness
Understand your inherited cancer risk for informed health decisions and planning.

Family Insight
Results can help guide testing and preventive care for your family members.

Early Action Advantage
Enable early screenings and preventive measures to reduce cancer development risk.

Precision Healthcare
Support tailored treatment options based on your unique genetic makeup.
How It Works
Simple Genetic Screening for Stronger Futures
DNA Sample Collection
A painless cheek swab or blood sample is collected at our lab or sent via a home kit.
Genetic Analysis
Advanced sequencing identifies mutations across multiple cancer-related genes.
Report & Genetic Counseling
Receive a clear report with expert-reviewed insights and recommended follow-up actions.
Why Choose FSG for Hereditary Cancer Screening
01
Advanced Genomic Technology
We use next-generation sequencing (NGS) for high accuracy and deep gene coverage.
02
Certified Genetic Experts
Reports are evaluated by licensed genetic counselors and clinical molecular specialists.
03
Timely & Confidential
Results are delivered within a week and handled with complete data privacy.
04
Trusted in the UAE
FSG is the UAE’s first certified stem cell and genomics laboratory.
FAQ’s
Frequently Asked Questions!
We’re here to help. Explore answers or reach out to our team directly.
Cancers that may be genetically inherited include breast, ovarian, colorectal, pancreatic, prostate, and endometrial cancers. These are often linked to inherited mutations in specific genes such as BRCA1, BRCA2, and those associated with Lynch Syndrome. Hereditary cancer genetic testing helps identify these mutations early, providing timely preventive care and risk management.
Hereditary cancer genetic testing using advanced methods like next-generation sequencing (NGS) is highly accurate. Most tests detect pathogenic variants with over 99% reliability. The results can provide powerful insights for personalized care planning when conducted through certified labs and interpreted by licensed genetic experts.
Hereditary cancer screening can detect an increased genetic risk for several cancers, including colon, breast, ovarian, endometrial, prostate, pancreatic, and melanoma. While genetic testing doesn’t diagnose cancer, it reveals inherited mutations that elevate cancer risk—supporting early surveillance and preventive strategies.
Testing for gene mutations is generally recommended by age 25 for individuals with a family history of breast or ovarian cancer. However, earlier hereditary cancer genetic testing may be advised based on personal or family history. Speak with a genetic counselor to determine the best time to begin hereditary cancer screening based on your risk profile.