Type
Blood Testing
Biomarkers
9
Duration
30 min
Results
21 days
Comprehensive genetic testing for hereditary cardiac conditions and heart disease risk factors. Identifies genetic variants associated with cardiovascular disease for personalized prevention strategies.
Genetic health tests analyze your DNA to identify inherited variants that may affect your health risks, medication responses, and nutritional needs. Unlike standard blood tests that measure your current state, genetic tests reveal your underlying predispositions — information that doesn't change over time and only needs to be tested once. Common panels examine variants related to cardiovascular risk (APOE, Factor V Leiden), medication metabolism (pharmacogenomics), methylation (MTHFR), nutrient processing, and disease susceptibility. This information can help personalize your preventive health strategy and medication choices.
Key Details
- Type
- DNA analysis (one-time test)
- Sample
- Saliva or cheek swab
- Turnaround
- 2–4 weeks
- Results
- Lifetime relevance — DNA doesn't change
- Common Use
- Risk assessment, pharmacogenomics
Who Is This For?
Anyone interested in personalized health insights based on their genetic makeup. People with a family history of genetic conditions who want to know their carrier status. Those wanting to optimize nutrition and supplementation based on genetic variants (e.g., MTHFR for folate metabolism). Patients who have experienced adverse medication reactions and want pharmacogenomic guidance.
What's Included
Preparation Required
No fasting required. Sample collection is typically a saliva sample or cheek swab — no blood draw needed for most genetic tests. Results take longer than standard blood tests because DNA analysis requires specialized laboratory processing.
Panel Categories
Biomarkers Tested
9The primary protein on LDL and VLDL particles. Each atherogenic lipoprotein particle carries exactly one ApoB molecule, making it a direct measure of the number of particles that can enter artery walls. Considered a superior predictor of cardiovascular risk compared to LDL cholesterol.
A protein produced by the liver in response to inflammation. CRP rises rapidly during infection, injury, or inflammatory conditions. It's a general marker — elevated CRP signals inflammation but doesn't pinpoint the source.
A protein essential for blood clotting that also serves as an inflammation marker. Elevated fibrinogen increases blood viscosity and clot risk, contributing to cardiovascular disease independent of cholesterol levels.
An amino acid produced during protein metabolism. Elevated homocysteine is an independent risk factor for cardiovascular disease, stroke, and cognitive decline. Levels are lowered by adequate B12, folate, and B6 intake.
A highly sensitive test for low-grade chronic inflammation linked to cardiovascular disease risk. Lower hs-CRP values are associated with better cardiovascular outcomes.
Often called 'bad' cholesterol, LDL deposits cholesterol in artery walls, contributing to plaque buildup and atherosclerosis. LDL is the primary target for cardiovascular risk reduction through diet, exercise, and medication.
Lp(a) is a cholesterol-carrying particle linked to genetic risk for heart disease. High levels increase cardiovascular risk.
Marker of heart stress and function
Troponin is a protein involved in heart muscle contraction. Elevated levels are a marker of heart damage, often used to diagnose heart attacks.
- Category
- Diagnostic
- Sample Type
- Saliva sample or cheek swab (varies by provider)
- Duration
- 30 min
- Results
- 21 days