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Our Developmental Nutrigenomic Panel, targets 35 genes to be analyzed for SNPs (single nucleotide polymorphisms). The report algorithms, created by our medical experts, will take the patient’s genetic results and create nutritional and lifestyle recommendations along with recommended lab work and health precautions based upon your DNA and our clinical experience. The built-in proprietary software, takes out the guess work and allows the provider to recommend the proper nutrition and health advisements based on your DNA results.
Regular Price $399.00
VALUEThis product provides information about results for some health conditions that are mostly influenced by genetics, and for other health conditions where genetics, environment, and lifestyle all influence your disease risk.
LIMITATIONSThis Test, is NOT a diagnostic product. This product evaluates specific variants associated with different health conditions and medication response. It does NOT look at all possible genes or variants associated with each condition tested. This product does NOT evaluate for gene variants associated with conditions not included in the test.
Perfect marriage of Innovative DNA Testing and Proprietary Interpretation Software.
Our Nutrigenomics tests, are much more than your typical laboratory’s DNA Genomic Test. In fact, our system is the perfect marriage between forward thinking Interpretation Software and Innovative Nutrigenomics Testing. In addition to being the most comprehensive DNA Nutrigenomics test available, the real magic lies within our proprietary SNP Interpretation software.
Our innovative software, takes the guesswork out of the physician’s results interpretation, as it links any identified SNPs to the recommended nutritional support that lends the greatest potential for the most optimal patient outcome. This software provides a detail and a summary, showing highly recommended nutritional support therapeutics, the nutritional or pharmacological support best left to the provider’s discretion, lifestyle recommendations, as well as any suggested additional laboratory testing one should consider.
This saves the provider valuable time that could be better spent on patient care, rather than looking up specific SNPs and the associated supplemental support. Additionally, the concise format of our report provides an easy to understand outline to better ensure alignment between patient and provider.