HEREDITARY GASTROINTESTINAL CANCER: CLINICAL EXOME PANEL (Sec. & CNVs) – 52 genes
LabGenetics
Delivery time
3-4 weeks
Sample
Blood
The Hereditary Gastrointestinal Cancer Panel covers the major tumor predisposition syndromes of the digestive tract. It includes genes for Lynch syndrome (MLH1, MSH2, MSH6, PMS2, EPCAM), familial adenomatous polyposis (APC), juvenile polyposis syndrome (BMPR1A, SMAD4), Peutz-Jeghers syndrome (STK11), Cowden syndrome (PTEN), hereditary diffuse gastric cancer (CDH1, CTNNA1), and genes for rare syndromes associated with pancreatoblastoma, intestinal carcinoma, and other gastrointestinal tumors (POLE, POLD1, MUTYH, NTHL1, AXIN2, CHEK2). This panel enables comprehensive molecular diagnosis, differentiating syndromes with specific prognostic and preventive implications. Genes analyzed: APC, MLH1, MSH2, MSH6, PMS2, EPCAM, PTEN, CDH1, STK11, SMAD4, POLE, POLD1, CHEK2, MUTYH, and others. You can consult the complete list of genes analyzed by contacting Genotica.
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