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Hereditary Nonpolyposis Colorectal Cancer (HNPCC) Multiplex Genetic Testing (Blood)

Published: August 9, 2026Updated: August 16, 2026

This test checks for genetic mutations linked to hereditary nonpolyposis colorectal cancer (HNPCC), a type of inherited cancer risk. It involves analyzing blood to identify specific DNA changes that may increase your risk of colorectal or other cancers.

Quick summary

["This test helps assess your risk for certain cancers linked to inherited genetic mutations."]

Medically reviewed by WellAlly Editorial TeamLast reviewed August 16, 2026Editorial policy

Key facts at a glance

LOINC
105197-8
Short code
HNPCC multi Bld/T
Synonyms
HNPCC multi Bld/T
Category
chemistry
Sample
whole-blood
Container
Lavender-top (EDTA)
Units
N/A
Fasting
false
Population
adult
Sex
all
Age range
18–65 years
Method
molgen
Specimen volume
3 mL
Stability
Room temperature: 4h, Refrigerated: 24h
Hemolysis max
0
Lipemia max
0
Icterus max
0
TAT
4–24 hours
Order
routine

Why This Test Might Be Ordered

Your healthcare provider may recommend this test if you have a strong family history of colorectal cancer, particularly multiple cases in close relatives, or if you have a personal history of certain cancers (like endometrial, ovarian, or small bowel cancers). It may also be suggested if you were diagnosed with colorectal cancer before age 50 or have other HNPCC-related symptoms.

What to Expect During the Test

A simple blood draw is used to collect a small sample. The lab will analyze your DNA for known mutations associated with HNPCC. Results are typically available within 2–4 weeks, depending on the lab’s processing time.

Understanding Your Results

Results can be categorized as negative (no mutations found), positive (mutations detected), or uncertain (limited genetic information). A positive result means you carry a mutation linked to HNPCC and may need closer monitoring or preventive strategies.

What Your Results Mean for You

If you test positive, your provider will discuss next steps, such as increased cancer screenings (e.g., colonoscopy at an earlier age), family counseling, or genetic counseling to manage risk and support you.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

Clinical Significance: HNPCC and Cancer Risk

Short name

HNPCC Genetic Screening

Frequently asked questions

What does this test measure?
This test detects specific DNA mutations in your blood that are linked to hereditary nonpolyposis colorectal cancer (HNPCC). It does not measure cancer itself but identifies genetic predispositions that may require additional monitoring or preventive care.
How often should I get this test?
This test is typically ordered once, usually during a genetic evaluation. If you test positive, your healthcare provider will recommend a personalized screening plan, often starting with regular colonoscopies or other cancer surveillance tests.
Can I fast before this test?
No fasting is required for this blood test. However, always follow your healthcare provider’s instructions for any specific preparations.
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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy