|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.
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.
(Downloadable documents are supplied within each kit dispatched)
|Price||Please contact us here|
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(Physicians use only)