The Hereditary Pancreatic Cancer Panel screens for mutations in 32 genes that are associated with increased risk of developing pancreatic cancer. This test is recommended for individuals with a family history of pancreatic, breast, or ovarian cancers, or those who have had pancreatic cancer at a young age. Understanding your genetic risk can influence surveillance strategies and inform family planning. The panel helps identify individuals who may benefit from more frequent screening, lifestyle changes, or preventive interventions. It’s also valuable in determining eligibility for clinical trials and targeted therapies in known carriers.
Our Tests
NIPT (Non-Invasive Prenatal Test) Gender
NIPT Gender is the simplest version of the NonInvasive Prenatal Test (NIPT), designed for parents who primarily want to know their baby’s sex early in pregnancy.
NIPT (Non-Invasive Prenatal Test) Basic
NIPT Basic is the entrylevel NonInvasive Prenatal Test designed to screen for the most common chromosomal conditions in pregnancy.
NIPT (Non-Invasive Prenatal Test) Standard
NIPT Standard is a more comprehensive version of the NonInvasive Prenatal Test, designed for parents who want deeper insights into their baby’s chromosomal health.
NIPT (Non-Invasive Prenatal Test) Plus
NIPT Plus is an advanced version of the NonInvasive Prenatal Test (NIPT) designed to give expecting parents the most comprehensive view of their baby’s chromosomal health.
Comprehensive Hereditary Cancer Test (~300 genes)
Covers breast, ovarian, colorectal, prostate, pancreatic, gastric, melanoma, endocrine, and more.
Hereditary Breast and Ovarian Cancer Test (50 genes)
BRCA1/2 and related genes for breast and ovarian cancer risk.
Hereditary Prostate Cancer Test (23 genes)
Genes linked to inherited prostate cancer risk.
Hereditary Pancreatic Cancer Test (32 genes)
Genes associated with inherited pancreatic cancer risk.
Hereditary Colorectal Cancer Test (44 genes)
Genes for Lynch syndrome and other colorectal risks.