GeneSavvy Starter Kit


Get started on the most actionable genetics platform in functional medicine with our simple saliva collection kit that can be completed from the comfort of your own home!
Once we receive your sample, we utilize the massive clinical power of Next Generation Sequencing (NGS) technology to extract your unique genetic information. When the lab processing is complete, you will receive a GeneSavvy Variant Exploration report that can be shared with your functional medicine team to develop more personalized, more effective health and lifestyle recommendations.

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  • Description


    The GeneSavvy Starter Kit includes:

    • Saliva DNA collection kit (other collection methods can be requested)
    • Enhanced Human Whole-Exome Sequencing (WES)
    • Mitochondrial Whole-Genome Sequencing (mtWGS)
    • Genetic data harmonized specifically for use with GeneSavvy’s analysis, 
 reporting, and research tools
    • Downloadable raw genetic data files (By request, we can provide your raw 
 data in standard genetic file formats)
    • GeneSavvy Variant Exploration Report (see details below)


    The GeneSavvy Variant Exploration Report that comes with the starter kit includes:

    • All Genetic Variants found by our Enhanced Human Whole-Exome Sequencing (WES)
    • All Genetic Variants found by our Mitochondrial Whole-Genome Sequencing (mtWGS)
    • Genotyping data and SNPs curated for functional medicine practitioners
    • HLA Subtypes found (Human Leukocyte Antigens)
    • KIR Subtypes found (Killer-cell Immunoglobulin-like Receptors)
    • RCCX gene module information
    • And more**

    **We are continuously pioneering new analysis tools to help identify functional genetic patterns between disease associated rare variants, lifestyle changing polymorphisms, real-time protein/enzyme activity, and environmental factors which we use to provide actionable options for vibrant life longevity. Many of these tools can be used to enhance and add information to your GeneSavvy reports without the need for cellecting new saliva samples and re-testing.


    Technical Information:

    Our testing was designed to sequence the exons and canonical splice sites (+/1,2) of the whole exome including extra coverage on genes and intron locations associated with medical disorders and treatment options. GeneSavvy has developed highly advanced protocols to target and extract variants and genetic features in exon regions, intron regions of interest, splice sites, and untranslated gene regions of interest with the following technical specifications:

    • 50x Depth of coverage for target regions
    • 500x Depth of coverage for mitochondrial regions
    • Specificity >98%
    • Sensitivity >94%

  • Additional information

    Additional information

    Weight 7.0 oz
    Dimensions 6.75 × 5 × 1.25 in
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