Multigene panel for hereditary cardiovascular and metabolic conditions (serum/plasma)
This test evaluates genetic markers linked to conditions affecting your heart, blood vessels, and metabolism through a blood sample.
It helps identify inherited risks for serious health issues that may require early monitoring or treatment.
Key facts at a glance
- LOINC
- 98037-5
- Short code
- Jewish Carrier Multigene Anl Bld/T
- Synonyms
- Jewish Carrier Multigene Anl Bld/T
- Category
- coagulation
- 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 variants in multiple genes associated with hereditary cardiovascular diseases (e.g., hypertrophic cardiomyopathy, aortic aneurysms) and metabolic disorders (e.g., familial hypercholesterolemia, diabetes-related conditions). Specific genes may include those linked to lipid metabolism, blood pressure regulation, or cardiac function.
Why It Matters for Your Health
Detecting these genetic variations can help your healthcare provider assess your risk for conditions that may not yet show symptoms, allowing for proactive lifestyle adjustments, medications, or monitoring.
Sample Collection and Processing
A blood sample is drawn from a vein in your arm. The serum or plasma portion is then analyzed for specific genetic sequences. This process is typically done in a laboratory and may take several days to complete, depending on the number of genes tested.
Common Conditions Evaluated
This panel may screen for conditions such as inherited heart rhythm disorders, vascular diseases, or metabolic syndromes that can affect blood pressure, cholesterol levels, or blood sugar control.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
Positive results may indicate a higher genetic risk for cardiovascular or metabolic diseases. These findings should be discussed with your healthcare provider to determine if additional testing, lifestyle changes, or preventive treatments are needed. Negative results mean no obvious genetic variants were detected in the tested genes, but other risk factors (like lifestyle or family history) may still apply.
Frequently asked questions
What does a positive result mean?
Will this test show all possible genetic risks?
How often should I get this test?
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