HEREDITARY COLORECTAL CANCER: CLINICAL EXOME PANEL (Sec. & CNVs) – 41 genes
LabGenetics
Delivery time
3-4 weeks
Sample
Blood
The Hereditary Colorectal Cancer Panel is designed to identify pathogenic variants in genes associated with genetic predisposition syndromes for colorectal cancer, such as Lynch syndrome (HNPCC), familial adenomatous polyposis (FAP), MUTYH polyposis, serrated polyposis, and other less common syndromes. These conditions are characterized by a high susceptibility to the early development of colorectal cancer and, in some cases, extracolonic tumors (endometrium, ovary, stomach, small intestine, or pancreas). Clinical exome sequencing and CNV detection allow for diagnostic confirmation, the development of personalized screening strategies, and preventive family counseling. Genes analyzed include: APC, MLH1, MSH2, MSH6, PMS2, MUTYH, POLE, POLD1, BRCA2, and others. You can consult the complete list of analyzed genes by contacting Genotica.
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