Genomic DNA from Whole Blood – Probe-Based Assay (Qualitative)
This test checks for the presence of specific genetic material (DNA) in your blood using a probe-based method. It may be used to screen or confirm certain genetic conditions.
["This test helps identify genetic variations that could influence health risks or conditions."]
Key facts at a glance
- LOINC
- 49447-6
- Short code
- T gondii DNA # Bld NAA+probe
- Synonyms
- T gondii DNA # Bld NAA+probe
- Category
- chemistry
- Sample
- whole-blood
- Container
- Lavender-top (EDTA)
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- probe-amp-tar
- 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 family history of genetic disorders, symptoms suggestive of a genetic condition, or if you’re at higher risk for certain inherited conditions. It can also be used to screen for conditions like cystic fibrosis, sickle cell disease, or other genetic markers before birth or in newborns.
How the Test Works
A small blood sample is taken, and the DNA is extracted. A specialized probe detects specific sequences of DNA in your sample. This method is highly sensitive and can identify genetic material even in small amounts.
Sample Collection and Preparation
Blood is drawn from a vein, typically in your arm. The sample is processed to isolate DNA, which is then analyzed using the probe-based technique. This process is usually painless and takes about 15–30 minutes.
What to Expect Before the Test
No special preparation is needed for this test. However, inform your healthcare provider about any medications, supplements, or recent illnesses that could affect results.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
This test can help diagnose or confirm genetic conditions, assess risks for inherited diseases, or guide prenatal testing. Early detection can lead to better management and treatment options. Results may also influence decisions about genetic counseling or family planning.
Short name
DNA Test (Qualitative)
Frequently asked questions
What Does a Positive Result Mean?
What Does a Negative Result Mean?
How Often Should This Test Be Repeated?
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