Genetic test for detection of specific DNA sequence variants using a probe (e.g., for hereditary conditions like Lynch syndrome or other genetic predispositions)
This test checks for specific DNA changes (mutations) that may increase your risk of certain cancers or other hereditary conditions.
["Identifies inherited genetic risks that may influence long-term health risks."]
Key facts at a glance
- LOINC
- 101556-9
- Short code
- C krusei DNA Ur Ql NAA+probe
- Synonyms
- C krusei DNA Ur Ql NAA+probe
- Category
- chemistry
- Sample
- urine
- Container
- Sterile urine container
- Units
- N/A
- Ref low
- 22
- Ref high
- 198
- Critical range
- — – 10000 N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- probe-amp-tar
- CPT
- 82553
- Specimen volume
- 10 mL
- Stability
- Room temperature: 2h, Refrigerated: 24h, Frozen: 7d
- Hemolysis max
- 0
- Lipemia max
- 0
- Icterus max
- 0
- TAT
- 4–24 hours
- Order
- routine
What This Test Measures
The test analyzes a sample of your DNA to detect particular genetic sequences (variants) that are linked to inherited conditions. These variants may be passed down through families and can influence disease risk, such as certain cancers or metabolic disorders.
How the Test Works
A specialized probe is used to identify specific DNA segments that match known variants. This is often done through advanced laboratory techniques like polymerase chain reaction (PCR) or next-generation sequencing to precisely locate these changes.
Why It Might Be Ordered
Your healthcare provider may recommend this test if you have a family history of certain cancers, genetic syndromes, or if you are at higher risk due to ethnicity or personal health history. It can also be used for preconception counseling or genetic counseling.
Sample Collection
You will provide a blood sample, saliva sample, or sometimes a buccal swab (inside cheek) to collect DNA. The lab processes this sample to extract and analyze the genetic material.
Reference range
Adult males: 22-198 U/L; Females: 22-198 U/LN/A
No special preparation required. Inform provider of any chest pain or symptoms.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
This test helps identify inherited genetic mutations that may increase susceptibility to specific diseases. Knowing your genetic profile can inform personalized healthcare decisions, such as monitoring, preventive measures, or risk-reducing strategies. It is particularly useful in guiding family planning and counseling for hereditary conditions.
Short name
Hereditary DNA Variant Probe Test
Frequently asked questions
What does a positive result mean?
How long will results take?
Are there any risks or side effects from 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.
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 17, 2026. · Read our editorial policy