Genomic DNA Analysis via Probe-Based Assay (for Specific Allele Detection)
This test checks for specific genetic variations in your DNA using a specialized molecular probe. It helps identify whether certain inherited or acquired mutations are present in your blood sample.
["This test may help diagnose or monitor conditions linked to specific genetic mutations."]
Key facts at a glance
- LOINC
- 106576-2
- Short code
- T palldm DNA Anal Ql NAA+probe
- Synonyms
- T palldm DNA Anal Ql NAA+probe
- Category
- chemistry
- Sample
- serum
- Container
- Red-top tube (SST)
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- probe-amp-tar
- CPT
- 86038
- Specimen volume
- 5 mL
- Stability
- Room temperature: 4h, Refrigerated: 24h, Frozen: 7d
- Hemolysis max
- 500
- Lipemia max
- 1000
- Icterus max
- 500
- TAT
- 4–24 hours
- Order
- routine
Why This Test Might Be Ordered
Your healthcare provider may recommend this test if you have a family history of genetic disorders, symptoms suggestive of a genetic condition, or if you’re at risk for conditions tied to the specific mutation being tested. It can also be used for carrier screening or pre-symptomatic detection in certain cases.
How the Test Works
A small blood sample is taken, and your DNA is extracted. A molecular probe designed to bind only to the specific mutation of interest is then used to detect its presence. This method is highly sensitive and precise for identifying genetic variations.
Sample and Preparation
The test uses whole blood collected in a special tube. No special preparation is needed, but fasting may not be required unless specified by your provider. Your sample is processed in a lab and analyzed for the target genetic mutation.
What to Expect After the Test
Results are typically available within 1–2 weeks. Your healthcare provider will discuss the findings with you, including whether the mutation was detected and its potential implications for your health.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
This test is used to confirm or rule out genetic conditions linked to the specific mutation being tested. Positive results may indicate an increased risk for inherited disorders, cancer predisposition, or other genetic syndromes. Negative results mean the mutation was not detected in this sample, but further testing may still be needed depending on clinical context.
Short name
DNA Mutation Screening (Allele-Specific Probe)
Frequently asked questions
What does a positive result mean?
Can this test detect all genetic mutations?
Is this test covered by insurance?
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 16, 2026. · Read our editorial policy