Genetic Full Mutation Analysis via Whole Blood DNA Sequencing
This test analyzes your DNA from a blood sample to identify specific genetic mutations that may be linked to inherited conditions or cancer risks.
["It helps doctors understand your genetic makeup for personalized medical advice."]
Key facts at a glance
- LOINC
- 94237-5
- Short code
- F2 gene Full Mut Anl Bld/T Seq
- Synonyms
- F2 gene Full Mut Anl Bld/T Seq
- Category
- chemistry
- Sample
- whole-blood
- Container
- Lavender-top (EDTA)
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- sequencing
- 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 examines a comprehensive set of genes for known mutations that could affect how your body functions. It looks for changes in DNA sequences that might increase the risk of certain diseases, including cancer, metabolic disorders, or other genetic conditions.
How the Test Works
A small blood sample is taken to collect DNA. Advanced laboratory techniques, including next-generation sequencing, are used to analyze thousands of genes for mutations. Results are compared against known genetic databases to identify any concerning variations.
Why It Might Be Ordered
Your healthcare provider may recommend this test if you have a family history of genetic disorders, if you’re at higher risk for certain cancers, or if you’re considering genetic counseling or carrier testing.
What to Expect Before the Test
No special preparation is needed. You’ll have a simple blood draw, similar to a routine lab test. If you’re undergoing this test for cancer risk assessment, you may discuss how results could impact treatment options with your doctor.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
Clinical Significance
Short name
Genetic Mutation Screen
Frequently asked questions
Identifying a mutation may confirm a suspected genetic condition, guide treatment decisions, or help family members understand their risk. Some mutations are associated with increased cancer risk, while others may indicate inherited disorders requiring specialized care.
How long will it take to get results?
What does it mean if my test is positive for a mutation?
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