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NEXTGEN HRR GENE PANEL GERMLINE, EDTA BLOOD

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NABL Cap Accredited 
The NextGen HRR Gene Panel (Germline) by Metropolis Healthcare evaluates genes involved in homologous recombination repair (HRR), a key pathway linked to hereditary cancer risk. This panel uses advanced next-generation sequencing on an EDTA blood sample to detect inherited variants affecting DNA repair. It helps identify predisposition to cancers such as breast, ovarian, prostate, and pancreatic cancer. The test supports early risk assessment, personalised screening, and appropriate clinical decision-making

 

  • 17 Crores+ Samples Processed
  • World Class Technology Labs
  • 25+ Years of Trust & Experience
  • Free Home Collection

Price: Rs. 24,150.00

Sample Type: EDTA BLOOD

Fasting Not Required


Notes:G8175

Frequently Asked Questions (FAQ's):

What does the NextGen HRR Gene Panel include?
It includes comprehensive sequencing of germline genes responsible for homologous recombination repair, which influence hereditary cancer risk.

How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses high-precision NGS technology to detect harmful variants across multiple HRR-related genes.

Who should take this test?
Individuals with a personal or family history of breast, ovarian, prostate, or related cancers should consider this panel.

Why is testing HRR genes important?
HRR gene mutations can increase cancer risk, and identifying them helps guide surveillance, prevention, and treatment strategies.

What sample is required for this test?
An EDTA blood sample is collected for germline DNA sequencing.

How reliable are the results at Metropolis Healthcare?
Metropolis Healthcare follows strict quality controls and validated sequencing protocols to ensure accurate genetic findings.

Can this test help in treatment planning?
Yes, HRR gene status may influence therapeutic decisions, including suitability for targeted therapies like PARP inhibitors.

Does this test assist in family counselling?

Yes, identifying germline variants helps assess hereditary risk for relatives and supports informed genetic counselling 

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