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Personalized DNA
Reports

Our DNA reports are designed to do more than just flag gene variants- they walk you through the actual metabolic pathways affected and explain how each gene functions in your body. Every report is personalized using your raw genetic data to highlight where your pathways may be underperforming and why that matters. You’ll learn what each gene does, how it fits into the bigger picture of your health, and what evidence-based “rescue strategies” may help reroute or support those functions. Whether it’s nutrient co-factors, lifestyle modifications, or deeper testing recommendations, these reports are built to empower you with knowledge and actionable insights- not overwhelm you with jargon.
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Personalized Mental Health and
Wellness Genomic Report

Our expanded Mental Health and Wellness Genomic Report is now available!
 

This in-depth report spans over 300 pages, covering the 44 most influential genes involved in mental health. It includes detailed explanations of the biopterin, dopamine, norepinephrine, epinephrine, serotonin, melatonin, glutamate, and GABA pathways, helping you understand how your unique genetics may influence mood, focus, and resilience.
 

We analyze over 1,000 SNPs (genetic variants) across these pathways. Your personal report will display your individual genotypes for each SNP available in your data file. (Not every SNP will appear in every report—availability depends on which testing service you used.)
 

We currently support raw data files from AncestryDNA, 23andMe, and the Ultimate Compatibility file from Sequencing.com.
 

Before purchasing, please make sure you’ve already downloaded your raw DNA data file from your testing provider. You’ll need to upload it during checkout so we can generate your personalized report.
 

Valued at over $150, this comprehensive report is now available for just $40, our way of making advanced genetic insights accessible to everyone.

Bonus: When our simplified short report is released, you’ll automatically receive it at no additional cost. It’s our way of saying thank you for being an early adopter of the expanded edition.

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What do you get in the genomic report?

Each report contains:
  • Comprehensive Pathway Guide that walks you through the pathway, gene-by-gene, and explains what physical symptoms or diseases/ disorders/ conditions may arise from reduced pathway function. 
  • Gene Information Cards that explain each gene in detail
  • Personalized gene variant report that lists your exact genotype and any studies specific to that SNP.​
  • Functional Pathway Map to give you an overview of the genes and how they interact.

 

Comprehensive Pathway Guide

Our Comprehensive Pathway Guide is a detailed, science-based resource that helps you understand the function and relevance of a specific biological pathway in your body. Each guide is designed to bridge the gap between your genetics and your health by exploring:
  • Overview of the Pathway
    A clear explanation of what the pathway does and how it supports key physiological processes such as detoxification, neurotransmitter synthesis, immune balance, or energy metabolism.
  • Genes and Proteins Involved
    A broad gene-by-gene walkthrough of the major enzymes and transporters.
  • Core Functions of the Pathway
    An overview of the metabolic, neurological, or cellular processes this pathway influences and why it’s essential for maintaining optimal health.
  • Diseases and Conditions Associated with Impairment
    A list of medical conditions or syndromes that have been linked in scientific literature to reduced activity or dysfunction of this pathway.
  • Symptoms of Impaired Function
    Common early warning signs or chronic symptoms that may suggest the pathway is under-functioning, even in the absence of a formal diagnosis.
  • Common Lab Markers That Reflect Pathway Status
    A list of clinical and functional labs that can provide insight into how well this pathway is operating (e.g., homocysteine, methylmalonic acid, serum folate, organic acids, inflammatory markers).
  • Nutrients and Co-Factors Required by the Pathway
    An overview of essential vitamins, minerals, and compounds the pathway depends on to function correctly (e.g., B2, B6, B12, folate, magnesium, zinc, SAMe).
  • Medications and Toxins That May Impair the Pathway
    A curated list of pharmaceutical agents, chemicals, and environmental toxins known to interfere with the enzymes or transporters within the pathway (e.g., methotrexate, nitrous oxide, glyphosate, anticonvulsants).
  • System-Level Impact and Interconnected Pathways
    A broader view of how this pathway links to other critical systems in the body such as how methylation influences detoxification, hormone regulation, neurotransmitter production, and DNA repair.
 
This guide is designed to complement the Gene Information Cards and your Personalized Genetic Variant Report and is intended for use alongside a healthcare provider trained in functional or genomic medicine. It serves as both an educational reference and a clinical support tool, helping to translate complex genetic information into actionable, real-world insight.

Gene Information Cards

Our Gene Information Cards offer an in-depth, clinically relevant look at each gene featured in your report. These cards are designed to help you (and your practitioner) understand how specific genetic variants may influence your biology, how that influence can show up in symptoms or lab work, and what can be done to support optimal function.

Each Gene Information Card includes:

  • Protein Name
    The name of the protein that the gene codes for, which may differ from the gene name itself. This helps connect your genetics to real biological function.

  • Alternative Gene or Protein Names
    A list of other names or abbreviations the gene/protein may be referred to in scientific or medical literature.

  • Chromosomal Location
    The precise region on your DNA where the gene is located, useful for deeper analysis or integration with genomic databases.

  • Protein Function
    A clear summary of what the protein does in the body, including its biological role and key functions in relevant pathways.

  • Protein Location and Tissue-Specific Activity
    Where the protein is most active (e.g., brain, liver, mitochondria, cell membrane), and how its function may differ based on tissue or cellular location.

  • Possible Symptoms of Reduced Protein Function
    Common symptoms, syndromes, or physiological signs that may occur when the protein is under-functioning or impaired due to genetic variation, nutrient deficiency, or environmental stressors.

  • Additional Conditions That May Further Reduce Protein Function
    Medical conditions, chronic stressors, or lifestyle factors that can compound the effects of a gene variant and further reduce protein efficiency.

  • Relevant Lab Markers
    Bloodwork or functional testing that may reflect protein dysfunction or downstream effects (e.g., elevated homocysteine, abnormal metabolites, nutrient depletion).

  • Rescue Strategies for Supporting Protein Function
    Evidence-based strategies to support or “rescue” the function of the protein. These may include nutrient cofactors, lifestyle interventions, targeted supplements, or clinical considerations.

 

These cards are designed to be both educational and actionable, helping bridge the gap between raw genetic data and personalized health decisions. They can be used as stand-alone references or in combination with your Pathway Guide and Variant Report for a full-spectrum view of your genomic health.

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Personalized Genetic Variant Report

Our Personalized Genetic Variant Report provides a detailed, science-backed summary of your individual genetic variants related to specific health pathways. This report is not just a list of SNPs—it integrates advanced validation methods to ensure that the data presented is both relevant and reliable.

Each report includes:

  • Gene Identifiers and Variant Details
    For each gene, the report lists relevant SNP identifiers (rsIDs), your personal genotype at that site, and your zygosity (homozygous ancestral, heterozygous, or homozygous variant).

  • Functional Context and Interpretation
    Where applicable, the report explains how your specific genotype may affect protein structure or function, including changes to enzyme activity, transport efficiency, or pathway dynamics.

  • Advanced Scientific Validation
    Each variant is supported by a combination of trusted data sources, including:

    • AlphaFold Missense Pathogenicity Predictions

    • ClinVar Classifications

    • Post-Translational Modification Site Analysis

    • Protein Domain and Structural Location

    • PolyPhen Predictions

    • Primary Literature References (PubMed, PMCID)

  • Clinical and Functional Insights
    When a variant has documented or suspected effects, the report provides information on associated symptoms, medical conditions, altered drug or nutrient interactions, or environmental risk factors.

  • Focus on Actionable Findings
    Rather than overwhelming you with rare or uncertain SNPs, the report highlights sites with functional significance, supported by strong scientific or clinical evidence.

 

This report is intended for use with a healthcare provider trained in functional medicine or clinical genomics. It is designed to support more informed decision-making and serve as a foundation for targeted nutritional, lifestyle, or therapeutic strategies.

Functional Pathway Map

Our Functional Pathway Map is a powerful visual tool included with your genomic report that brings your biology to life. Rather than presenting isolated gene variants, this map shows how your genes work together in the context of real biochemical pathways and where dysfunction may occur based on your unique genetic profile.

Each map is tailored to your data and includes:

  • Clear, easy-to-follow visuals of core metabolic, detoxification, methylation, or neurotransmitter pathways

  • Supplementation points to support or bypass impaired enzymes or transporters

  • Medication interactions and where certain drugs may inhibit or alter pathway function

  • Clinical context for how pathway disruptions can contribute to symptoms, conditions, or treatment resistance

  • Integrated systems view, showing how one pathway connects to others in your body

 

Our goal is to give you and your healthcare provider a functional, systems-based view of your genetics that helps you move from raw data to real, actionable insight. Whether you're looking to optimize wellness or manage complex conditions, our Functional Pathway Map empowers you to see the full picture.

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Join our mailing list and be the first to know when our Personalized DNA Reports are released!

Contact us:
geneticsforthepeople@gmail.com

 

© 2025 Genetics for the People. All rights reserved.

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