Genetic analysis of DNA using a probe for specific nucleotide sequences (qualitative)
This test checks for specific genetic variations in your DNA using a molecular probe. It helps identify whether certain genes are present or altered in a way that may influence health risks or conditions.
["This test can help determine if you carry genetic markers linked to inherited conditions or risks."]
Key facts at a glance
- LOINC
- 63429-5
- Short code
- uidA gene Spec Ql NAA+probe
- Synonyms
- uidA gene Spec 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
- 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
What This Test Measures
The test detects specific DNA sequences using a labeled probe. The probe binds to matching genetic material, allowing for qualitative confirmation of presence or absence of those sequences. This is often used in genetic screening, carrier testing, or research contexts.
How the Sample is Collected
A blood sample is typically taken from a vein in your arm. The DNA is extracted from your white blood cells and prepared for analysis. No special preparation is needed, but fasting may not be required unless specified by your healthcare provider.
When This Test Might Be Ordered
Your healthcare provider may recommend this test if you have a family history of genetic disorders, if you’re considering genetic counseling, or if symptoms suggest a genetic condition. It can also be used for prenatal screening, carrier testing for inherited disorders, or research purposes.
What to Expect Before the Test
There are usually no specific preparations needed. You may experience mild discomfort from the needle, but most people tolerate the procedure well. If you’re pregnant or have a bleeding disorder, let your provider know before the test.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
◆Associated findings1
Frequently asked questions
Why might my doctor order this test?
How long will it take to get my results?
What if my test results are positive for a genetic variation?
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