Genetic mutation detection in whole blood (next-generation sequencing)
This test checks for specific genetic mutations in your blood using advanced sequencing technology to identify variations in DNA that may influence health risks or conditions.
["Helps identify inherited or potential disease-causing mutations for personalized medical guidance."]
Key facts at a glance
- LOINC
- 106870-9
- Short code
- NGR1 gene Mut Anl Bld/T
- Synonyms
- NGR1 gene Mut Anl 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
What This Test Measures
The test analyzes DNA extracted from your whole blood sample to detect known genetic mutations. It identifies changes in your genetic code that could be linked to conditions like cancer, metabolic disorders, or inherited diseases. Results may highlight mutations in genes associated with your specific health concerns or family history.
How the Test Works
Your blood sample is processed to isolate DNA. Next-generation sequencing technology reads the DNA sequence in high detail, comparing it against known reference sequences to pinpoint mutations. This process is highly sensitive and can detect even small genetic changes.
Preparation for the Test
No special preparation is needed. You may eat or drink as usual before your blood draw. The test uses a simple blood sample collected by a healthcare professional.
Common Uses and Indications
This test is often used for genetic screening, diagnosis of inherited conditions, or monitoring risks for certain diseases. It may also be part of a broader genetic evaluation if you have a family history of genetic disorders or if symptoms suggest a genetic basis for your health concerns.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
Clinical Significance
Short name
Genetic Mutation Test (blood)
Frequently asked questions
Why might my doctor order this test?
What does a positive result mean?
What if the test is negative?
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