myRisk® Test

 

Test myRisk® Test – Hereditary Cancer Gene Panel
Gene 25 genes: BRCA1, BRCA2, APC, ATM, BARD1, BMPR1A, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, EPCAM, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, PMS2, PTEN, RAD51C, RAD51D, SMAD4, STK11 and TP53
Disease Hereditary Breast, Ovarian, Colon, Endometrial, Pancreatic, Prostate, Gastric, and Melanoma cancers
Method NexGen sequencing, Long Range PCR and large genomic rearrangement assays (MLPA and CGH), (99.92%, analytical sensitivity)
Notes myRisk® focuses on clinically actionable mutations that increase risk for a number of cancers. Cancer is complex as multiple genes can cause a single cancer type or multiple cancers can be linked to a single gene.

  • Clinically actionable results
  • Minimum depth of coverage: 50x

All findings with NGS will be confirmed with orthogonal site specific Sanger sequencing method.

Specimen Peripheral blood (2x9mL EDTA) or genomic DNA (3.5µg)
Turn Around Time Standard Service:   30 Business days
Shipping Room temperature, delivered within 72hrs for blood, no time constraints for DNA.
Refrigerate blood if storage is required prior to shipping, do not freeze.
More Information
Required Documents
(Downloadable documents are supplied within each kit dispatched)
  1. Patient Informed Consent Form
  2. Physician Test Request Form
  3. Payment Form (private patients only)
  4. Customs Declaration Form (international patients only)
  5. Import Permit Blood/DNA/Tissue (international patients only)
Price Please contact us here
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