Hereditary Nonpolyposis Colorectal Cancer (HNPCC) Multiplex Genetic Testing (Blood)
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.
["This test helps assess your risk for certain cancers linked to inherited genetic mutations."]
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?
How often should I get this test?
Can I fast before this test?
Sources
- 1
- 2Lab Tests OnlineSource
- 3
Click any link to access the full source. PubMed Central (PMC) links provide free full-text access.
This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy