Familial GI Cancer (Lynch syndrome, Gastric, Pancreas, Polyposis)
| Test Information | |
|---|---|
| Test Name | Familial GI Cancer (Lynch syndrome, Gastric, Pancreas, Polyposis) |
| Lab (Location) | University Health Network |
| Category | Cancer |
| Subcategory | Hereditary Gastrointestinal Cancer |
| Gene/Platform/Region List | APC, ATM, BMPR1A, BRCA1, BRCA2, CDH1, CDKN2A, CHEK2, CTNNA1, EPCAM, GALNT12, GREM1, MLH1, MLH3, MSH2, MSH3, MSH6, MUTYH, NTHL1, PALB2, PMS2, POLD1, POLE, PTEN, RNF43, RPS20, SDHB, SDHD, SMAD4, STK11, TP53 |
| Test type | Gene Panel |
| Samples Accepted | Blood, DNA, Saliva |
| Indications Diagnosis | Diagnosis, Carrier / Cascade Testing |
| Test Methodology | CNV, Sequencing |
| Methodology Notes | EPCAM and GREM1 CNV only |
| Diseases/Conditions | Gastrointestinal Cancer, Lynch syndrome, Gastric cancer, Pancreas cancer, Polyposis |