Comprehensive Genetic Panel for Cardiovascular Disease Risk Markers (Blood)
This test evaluates genetic markers linked to increased risk for heart disease, stroke, or other cardiovascular conditions through blood analysis.
["Assessing your genetic predisposition to heart-related health risks with a simple blood draw."]
Key facts at a glance
- LOINC
- 93201-2
- Short code
- CHD-DNA
- Synonyms
- CHD Multigene Anl Bld/T
- Category
- chemistry
- Sample
- whole-blood
- Container
- EDTA (lavender-top) tube for whole blood; sterile container for tissue specimens
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- ≥ 0 years
- Method
- molgen
- CPT
- 81405
- SNOMED
- 443968002
- Specimen volume
- 5-10 mL whole blood; 5-10 mg tissue
- Stability
- Whole blood: Ambient 24 hours; Refrigerated (2-8°C) up to 7 days; Frozen (-20°C or lower) for long-term storage. Tissue: Frozen at -80°C preferred; refrigerated acceptable for short term.
- Hemolysis max
- 0
- Lipemia max
- 0
- Icterus max
- 0
- TAT
- 168–720 hours
- Order
- routine
What Does This Test Measure?
The test analyzes multiple genetic variants associated with cardiovascular health, including those linked to cholesterol metabolism, blood pressure regulation, and inflammation. Some components may also assess inherited traits affecting blood lipids or blood vessel function.
Why Might You Need This Test?
Your healthcare provider may recommend this test if you have a family history of heart disease, high cholesterol, hypertension, or other cardiovascular conditions. It can also help identify genetic risks in individuals with unexplained cardiovascular symptoms or those at high risk for developing these conditions.
How Is the Test Performed?
A small blood sample is drawn from your arm by a healthcare professional. The sample is then processed in a lab to detect specific genetic markers. Results are typically available within 1–2 weeks, depending on laboratory processing times.
What Are the Possible Findings?
Results may indicate whether you carry genetic variants that could influence your risk for cardiovascular disease. Some findings may suggest higher or lower risk compared to the general population, but they are not definitive diagnoses. Your provider will discuss these results in the context of your overall health.
Reference range
Interpretation provided as presence or absence of pathogenic variants, variants of uncertain significance (VUS), or benign variants in genes associated with coronary heart disease (e.g., LDLR, APOB, PCSK9, LPA, 9p21 locus). No quantitative reference range applies; results reported as genetic variant classification.N/A
No fasting required. Patient should be informed about genetic testing implications. Informed consent recommended due to hereditary nature of results. Pre-test genetic counseling is advised. Provide relevant family history of coronary heart disease, hyperlipidemia, or sudden cardiac death.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
◆Associated findings1
Short name
CardioGenetic Blood Test
Frequently asked questions
How long will it take to get my results?
This test focuses on genetic markers that may increase your risk for cardiovascular disease, not on diagnosing existing conditions. If you have symptoms or a confirmed diagnosis of heart disease, additional tests (like standard blood work or imaging) would be needed to assess current health status.
Genetic test results should be interpreted by your healthcare provider in combination with lifestyle factors, medical history, and other health data. While some genetic variants may suggest higher risk, lifestyle modifications (such as diet, exercise, and stress management) can still significantly reduce cardiovascular risk regardless of genetics.
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