MY DNA

Personalized Nutrigenomic Health Report

The MY DNA report includes 12 panels and analyzes over 1500 mutations from your entire genome, using whole genome sequencing, to give you the most comprehensive genetic test. The clinical significance of each mutation has been manually curated by our trained genetics team and is based on the latest peer-reviewed scientific literature. The invaluable information within the MY DNA report will allow you to learn more about your unique genetic makeup and how it can play a role in your overall well-being.

The MY DNA report offers insights into yourself that are unattainable through other methods. Through genetic testing, you gain valuable information to empower you in making immediate and long-term adjustments to support your wellness goals. While not all genetic predispositions can be prevented, awareness of your risks enables proactive monitoring for any worrisome symptoms, facilitating timely and effective treatment. Additionally, such awareness can help inform future generations of potential risks. Genetic testing also reveals predispositions that may be mitigated through appropriate nutrition, exercise, and other wellness habits. The MY DNA report serves as a gateway to achieving optimized health, wellness, and realizing your envisioned life.

What the MY DNA Report Includes: 12 Comprehensive Health Panels

Each panel delves into specific traits related to its area of focus. For instance, our Cardiometabolic panel uses the latest genetic research to assess your individual risk for ten known areas of concern, such as stroke, heart attack, and diabetes. We refer to these areas of concern as traits.

The MY DNA report evaluates your health risks by comparing your genetic data to pioneering genetic research. By analyzing the risk impact of each mutation, prioritizing traits based on your unique genome, and categorizing them as High, Medium, Low, or Superpower, the report guides you in identifying immediate priorities and potential strengths when it comes to your health. Traits ranked as high-priority indicate areas needing closer attention due to heightened genetic risk, empowering you to tailor a personalized supplement regimen based on your DNA. If any high-priority traits cause concern, seeking additional medical testing is recommended for further evaluation.

Key Elements and Features of MY DNA

Uncover Your Genetic Weaknesses: Genetic testing provides valuable insights into an individual's predisposition to illnesses. Given this information, healthcare professionals can create personalized care plans, including lifestyle adjustments and regular monitoring, to mitigate risks and improve outcomes. This proactive approach empowers individuals to take control of their health and potentially prevent disease onset or progression.
Personalized Nutrition Recommendations: Genetic testing reveals variations that affect how individuals respond to nutrients like carbohydrates, fats, vitamins, and minerals. Armed with this knowledge, people can customize their nutrition plans to meet their specific needs, supporting overall health. For example, someone with a gene variation that impacts vitamin D synthesis may need to adjust their diet or take supplements accordingly to reach healthy vitamin D levels. Tailoring nutrition to genetic makeup optimizes health and lowers the risk of developing certain conditions.
Discover Your Targeted Medication Regimen: Genetic testing can uncover drug-gene interactions by identifying variations in genes responsible for metabolizing medications. For individuals with such variations, drugs may be metabolized differently, affecting their effectiveness and potentially causing adverse reactions. With this information, healthcare providers can prescribe the most suitable medications for each individual, optimizing treatment outcomes and minimizing risks.
Achieve Your Health and Wellness Goals: This crucial information about your health can only be discovered through genetic testing. It enables you to make informed decisions about your health before problems arise, efficiently tackle current health concerns, and elevate your overall wellness to the next level.

How MY DNA Unlocks the Power of Your DNA

The Human Genome & You

The human genome is like your biological instruction manual, made up of four basic building blocks called nucleotides: adenine (A), thymine (T), guanine (G), and cytosine (C). These nucleotides pair up to form the famous double helix structure of DNA, which is organized into 23 pairs of chromosomes. Genes, found within chromosomes, contain instructions for making proteins that determine everything from your traits, like eye color and height, to your potential to develop chronic health conditions. You inherit one chromosome from each parent, explaining why you may resemble them. Despite having billions of nucleotides and thousands of genes, you actually have two copies of each part of your genome, making it incredibly complex. Scientists use the human reference genome as a guide to understand what's considered "normal" in human DNA.

The Genome is Unique

Each person's genome differs at around 84 million spots. To capture this wide variation, this test examines your entire genome, unlike other tests that just focus on select areas. When DNA is being copied, mutations in the genome can happen randomly. A single nucleotide, like a T, can be accidentally replaced with a G, creating a mutation. These mutations are called single nucleotide polymorphisms (SNPs), meaning a single nucleotide changed at that position in the genome. Within DNA, there are two general areas, one being actual genes and the other being large sections of DNA that support the expression of genes. SNPs that occur within genes can affect the actual protein function, while variations outside genes can lead to different biological outcomes, such as more, less or none of a protein being produced.

Your Genome Can Affect Your Health

SNPs can significantly affect vital body mechanisms, potentially influencing the likelihood of certain health conditions. In this report, each SNP is categorized as either a risk or beneficial SNP depending on its impact on the gene. With two copies of each gene, individuals may carry zero, one, or two variant alleles at each SNP site, collectively termed as their genotype. Your genotype shapes how the SNP affects your health.

Epigenetic Factors: Nature vs Nuture

The MY DNA test reports solely on your genome and should not be used as a clinical diagnostic tool. This is because epigenetic factors such as diet, lifestyle, activity level, microbiome diversity, and environment also influence health risks by affecting gene expression. While reports may highlight high-risk traits based on DNA, symptoms may not always manifest due to daily choices and environmental factors. Some traits are gender-specific, which are included for everyone to provide insights into potential risks for offspring. If any trait concerns you, it is advisable to consult a medical professional.

Steps to Complete the MY DNA Lab Test

You will receive your MY DNA kit and follows the directions on the instruction card provided to register your kit at nbresults.com.
Collect your DNA sample using a simple cheek swab, then send the DNA sample back using the prepaid envelope provided.
After mailing the DNA sample to the lab using the prepaid return envelope provided, the DNA sample is received, sequenced, and the data is analyzed.
Once processing is complete and the DNA sample has been fully sequenced and analyzed, your MY DNA report will be generated and available.

If you have any questions throughout the process, please contact our clinic for further assistance by calling (586) 703-0228, or emailing store@nuvisionhealthcenter.com

Disclaimer: This report has not been evaluated by the Food and Drug Administration. Therefore, this report is intended for informational use only. It is not intended to diagnose, treat, cure, or prevent any disease. Any treatment decisions based on these results should only be made after consulting a licensed medical professional, who can confirm any concerning results with additional clinical testing. Furthermore, before implementing any recommendations, be sure to inform your practitioner of all medical information, including relevant lifestyle choices, family medical history, pre-existing medical conditions, and any supplements or medications you are already taking, as they can influence your personal health needs.

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