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 Basic is the entrylevel NonInvasive Prenatal Test designed to screen for the most common chromosomal conditions in pregnancy.
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 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.
Covers breast, ovarian, colorectal, prostate, pancreatic, gastric, melanoma, endocrine, and more.
BRCA1/2 and related genes for breast and ovarian cancer risk.
Genes linked to inherited prostate cancer risk.
Genes associated with inherited pancreatic cancer risk.
Genes for Lynch syndrome and other colorectal risks.
This focused test analyzes 32 genes, including BRCA1/2, PALB2, CDKN2A, and STK11, to detect inherited risks for pancreatic cancer.
Although less common, pancreatic cancer is often aggressive and diagnosed late. About 5–10% of cases are hereditary. Identifying risk early helps families take preventive action.
BRCA1, BRCA2, PALB2, CDKN2A, STK11
ATM, TP53, MLH1, MSH2, MSH6, PMS2, PRSS1, SPINK1
BRCA1/2, PALB2, CDKN2A, STK11
CDH1 (hereditary diffuse gastric cancer)
CDKN2A, BAP1
RET (MEN2), VHL, SDHx genes, PTEN
Li‑Fraumeni syndrome (TP53)
Kidney cancers (FH, FLCN, VHL)
Brain tumors and sarcomas
Order the test online or through your provider
Provide a saliva or blood sample
Receive your report securely
Order Your Hereditary Pancreatic Cancer Test Today
Upgrade option: Comprehensive Hereditary Cancer Test (~300 genes).
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