Hereditary pancreatic cancer [14 genes]

Given the high mortality associated with this disease, identifying patients at risk for developing pancreatic cancer is essential to establish follow-up programs that lead to early detection of this disease. In the presence of exocrine pancreatic cancer, our recommendation would be to study the following genes.

10-15% of pancreatic cancer are due to a predisposition syndrome towards hereditary cancer.

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Steps to follow
Steps to follow
Click here to see the Guidelines for the collection and transport of biological samples

1) Download & fill out

Please cover as many fields as possible in both documents

2) Sample collection

See sample types in the guidelines

3) Pack the sample

Please pack the sample in a way to prevent leakage

4) Send the sample & the request

Please schedule the delivery for Monday–Friday: 8am – 5pm

5) Result: the report

Via: e-mail and/or through the customer portal

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Hereditary pancreatic cancer

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Consentimiento*
Technique: NGS capture panel

Turnaround time (TAT): 15 days

Ref. S-202211931

Updated (dd/mm/yy): 07/10/2025

Hereditary pancreatic cancer: View panel
  • APC
  • ATM
  • BRCA1
  • BRCA2
  • CDKN2A
  • FANCG
  • MLH1
  • MSH2
  • MSH6
  • PALB2
  • PMS2
  • PRSS1
  • STK11
  • TP53

Priority Genes : Genes where there is sufficient evidence (clinical and functional) to consider them associated with the disease; they are included in the clinical practice guidelines.
Secondary Genes: Genes related to the disease, but with a lower level of evidence or that constitute sporadic cases.
* Candidate Genes: Not enough evidence in humans, but potentially associated with the disease.

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