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Within every patient’s genome are opportunities to optimize health and wellness. Genetic
testing can empower practitioners with information that can enhance patient management
and clinical outcomes. But the translation of genetic testing to effective clinical decisions
can be challenging.
PureGenomics® is a platform combining educational tools, protocols and core
products with our dynamic, practitioner-exclusive website application designed to help
identify common genetic variations known as Single Nucleotide Polymorphisms (SNPs) that
are clinically relevant and nutritionally actionable. This unique platform makes it easy to TEST,
TRANSLATE and TARGET SNPs with the right nutritional support, empowering practitioners with precision
and confidence in the pursuit of optimal health for every patient.*
Testing for common genetic variations enables practitioners to more effectively treat patients and their individual needs.
Single Nucleotide Polymorphisms (SNPs) are common genetic variations that explain many of the differences between individuals.
Knowing which SNPs a patient carries allows for greater precision in nutritional recommendations.*
Select from the recommended products that provide specialized support with ingredients at clinically relevant doses,
and in clinically relevant forms.*
Discover a new level of precision in everyday practice with PureGenomics®.