Pharmacogenomics
Discuss reported genetic variants that may affect how certain medications are processed. Treatment decisions remain with your clinician.
Whole Genome Sequencing
More of your DNA.
More context for your care.
Your clinical team reviews your results alongside your health history and goals, then helps you understand what they mean for your care—including personalized supplement and peptide recommendations when appropriate.
Your test includes an at-home collection kit and a one-on-one results review, so you leave with greater understanding and clear next steps.
$899 GENETIC TESTING
What’s included
- 800+ biomarkers analyzed — methylation, MTHFR, vitamin and mineral deficiencies, hormone metabolism, detox pathways, and more
- Complete at-home test kit — blood sample collection, urinalysis, and cheek swab
- Results in 5–7 business days after the lab receives your sample
- Home delivery of your kit with prepaid return shipping to our partner laboratory
- One-on-one review of your report with our clinical team
- Personalized peptide and supplement recommendations based on your results, health history, and clinical review, when appropriate
Understand the findings.
Consider the full picture.
Genetic information is one part of your health story. A clinical review brings your report together with your history, current medications, symptoms, and any additional testing.
Inherited risk
Explore relevant findings and whether they warrant further assessment. A genetic risk does not mean a condition will develop.
Wellness insights
Review available nutrition, metabolic, and other wellness findings in context. Genetic results alone do not establish a vitamin deficiency or determine a hormone or peptide treatment.
A broader view of your genetic makeup.
Whole genome sequencing looks across both protein-coding and non-coding regions of your DNA. That broader scope can reveal genetic variation beyond the specific locations examined by a targeted test.
Targeted genetic testing
Examines selected genes or known variants to answer a particular question. Its value depends on what the test is designed to detect.
Whole genome sequencing
Uses sequencing technology to examine DNA across the genome, including regions outside protein-coding genes. It can identify a wider range of variants, although not every finding has a known health meaning.
Insights you can discuss
Your clinician helps distinguish findings that may influence your care from those that need more evidence or follow-up. The report is a starting point for informed decisions.
What your results can help you explore.
Your report opens a more focused conversation about your health. The insights available depend on the variants and biomarkers reported by the laboratory.
Methylation & nutrient status
Review findings related to methylation pathways, including MTHFR, alongside nutrient measurements and your health history. Genetic findings can add context; they do not, by themselves, establish a vitamin or mineral deficiency.
Hormone metabolism
Discuss reported hormone-related findings alongside symptoms and appropriate blood work. Your clinician uses the complete picture when considering hormone care.
Metabolic pathways
Explore reported findings related to how your body processes nutrients and other substances. Discuss which findings are relevant to your goals and whether additional evaluation would help.
Laboratory precision.
Clinical perspective.
Your sample is analyzed in a CLIA-certified laboratory using next-generation sequencing at an average of 30× coverage. This means DNA positions are read an average of 30 times, supporting a reported sequencing accuracy above 99.9%. Sequencing accuracy describes the laboratory measurement; it does not mean every genetic variant is detected or that health predictions are certain.
What your $899 includes.
An at-home testing experience, a detailed report, and a dedicated conversation about what to do next.
Testing from home
Your collection kit includes instructions for the required blood sample, urine sample, and cheek swab. Your kit ships directly to your door and includes prepaid return shipping to our partner laboratory.
A personal results review
Meet one-on-one with our clinical team to discuss your report, ask questions, and connect the findings with your symptoms, history, and priorities.
Recommendations for you
Your review can inform a personalized care plan, including supplement and peptide recommendations when clinically appropriate. Recommendations are physician-reviewed before your plan is finalized. Testing does not guarantee a prescription or a particular treatment.
Information to revisit over time.
As scientific understanding develops, the interpretation of genetic findings can change. Keep a copy of your report to share with your clinician as your health needs evolve. Future reanalysis and updated reports depend on the laboratory’s services and are not automatically included.
From kit to clarity.
We help you understand the testing process and where your results fit into your care.
Explore the test
Contact Vale to discuss the offering, cost, collection instructions, and consent before proceeding.
Collect and return
Follow the instructions supplied with your at-home kit and return the required sample materials to the laboratory.
Review your report
Discuss your results with the clinical team, including the meaning and limitations of reported findings.
Plan your next steps
Your clinician can consider whether follow-up testing, genetic counseling, or changes to your care are appropriate. Recommendations are individualized.
What to know. Sequencing does not detect every genetic change or predict every health outcome. Some results may be uncertain and may have implications for relatives. Review the laboratory’s consent and privacy information before testing.
Learn more about genome sequencing and genetic testing.
Whole Genome Sequencing
Your next step toward
more personalized care.
At-home testing, a one-on-one results review, and physician-reviewed recommendations tailored to you.
$899
Preview your order. Online purchasing opens soon.