Genetic Screening Panel
Type
Blood Testing
Duration
25 min
Results
21 days
Basic genetic screening for common hereditary conditions.
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.
- Category
- Diagnostic
- Sample Type
- Saliva sample or cheek swab (varies by provider)
- Duration
- 25 min
- Results
- 21 days