Complete Blood Panel with Genetic Variant Screening (Full Blood Test with Genetic Analysis)
This test evaluates your blood components and checks for specific genetic variations that may influence how your body processes certain substances.
["Assesses blood health and genetic factors that could affect metabolism or disease risk."]
Key facts at a glance
- LOINC
- 64431-0
- Short code
- KIR3DP1 full variant Bld/T Ql
- Synonyms
- KIR3DP1 full variant Bld/T Ql
- 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 includes standard blood counts (red blood cells, white blood cells, platelets) and measures the concentration of various substances in your blood, such as electrolytes, proteins, and enzymes. It also includes a genetic screening component to identify specific DNA variations that may be relevant to your health.
Blood Components and Chemistry
Your blood sample is analyzed for red blood cell count, hemoglobin levels, white blood cell differential, platelet count, and other markers like sodium, potassium, glucose, and liver enzymes. These help assess overall health, hydration, organ function, and potential blood disorders.
Genetic Variant Screening
A portion of your blood is used to extract DNA for screening specific genetic variants. These variants may be associated with conditions like metabolic disorders, certain cancers, or drug responses. The results help identify potential hereditary risks or genetic predispositions.
How the Test Works
Blood is drawn from a vein in your arm. The sample is processed to separate components for standard blood testing and genetic analysis. Results are generated through automated laboratory equipment and genetic sequencing technology.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
Clinical Significance
Short name
Full Blood Test with Genetic Variant Check
Frequently asked questions
This test is useful for diagnosing blood-related conditions, monitoring chronic diseases, and identifying genetic risks that may influence treatment options or long-term health. Early detection of genetic variants can guide preventive care or targeted therapies.
How long will I need to prepare for this test? There are no special preparations needed. You may be asked to fast for certain blood chemistry tests, but the genetic portion does not require fasting.
Will the results affect my treatment plan? Results may influence your healthcare provider’s decisions regarding diagnosis, monitoring, or personalized treatment options based on blood chemistry and genetic findings.
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