Genetic Report Summary (Whole Blood)
This test provides a summary of genetic analysis performed on a sample of your blood to identify potential genetic variations that may influence health risks or conditions.
["A genetic report helps assess inherited traits or risks that may require further medical evaluation."]
Key facts at a glance
- LOINC
- 50399-5
- Short code
- Deprecated Clin genetic rpt sum Pnl Bld/
- Synonyms
- Deprecated Clin genetic rpt sum Pnl Bld/
- Category
- chemistry
- Sample
- whole-blood
- Container
- Lavender-top (EDTA)
- Units
- N/A
- Ref low
- 0.8
- Ref high
- 1.2
- Critical range
- — – 5 N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- molgen
- CPT
- 86140
- SNOMED
- 396252006
- 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 from your blood sample to detect specific genetic markers. These markers may relate to inherited conditions, metabolic functions, or other genetic traits. Results are interpreted by a healthcare provider to identify any relevant findings.
Sample Collection and Preparation
A blood sample is collected by a healthcare professional. The sample is processed to extract DNA for genetic analysis. Results are generated based on the detected genetic variations.
Common Uses and Considerations
Genetic reports are often used in prenatal testing, carrier screening, or assessing inherited risks for conditions like certain cancers, metabolic disorders, or cardiovascular diseases. They may also help guide personalized treatment plans.
How Results Are Interpreted
Results are reviewed by a genetic counselor or healthcare provider to determine clinical significance. Variations may be classified as normal, uncertain, or potentially concerning, depending on known medical associations.
Reference range
INR: 0.8-1.2 (warfarin: 2.0-3.0)N/A
Inform your healthcare provider if you are taking blood thinners. No special preparation required.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
Genetic variations identified in this test can influence health risks, including inherited disorders, drug metabolism, or predispositions to certain diseases. While some findings may be common in the population, others may require further medical evaluation or monitoring. Always discuss results with your healthcare provider to understand implications for your health.
Short name
Genetic Screening Report
Frequently asked questions
Why might I need this test?
What does a positive or abnormal result mean?
How long will it take to get my results?
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