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Health

Genetic Predispositions Test

Starting from $399

Anticipate possible health risks with your DNA. See how your genes can influence your susceptibility to common diseases with our Genetic Predispositions Test. More information

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Saliva Sample

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Processed within 30 to 60 days

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Covered by most health insurances

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Report is approx. 1000 pages

Choose 0 Additional Report

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Price with options $399

Testimonials

“Very professional service, simple and clear!
Well detailed reports, even including suggestions to improve our fitness, health and skincare!
I'm very happy with my experience, highly recommend.”

- Annabelle

Take advantage of your kit to save on additional reports
$50 for each additional report
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Additional information

Genetic Predispositions Test - Anticipate Possible Health Risks with Your DNA

This comprehensive test analyzes over 700,000 genetic markers to assess your predisposition to a wide range of health conditions and diseases, providing you with valuable insights to anticipate and manage your risks.

What You Will Discover:

  • Biometric Predispositions: Identify potential risks for health conditions such as type 1 diabetes and get an overview of your predisposition compared to the general population.
  • Complex Diseases: Receive information on genetically based diseases and complex conditions to better understand the risk factors relevant to you.
  • Biomarkers and Pharmacogenetics: Analyze important biomarkers and discover how your genetic profile may influence your response to medications for a more personalized approach to treatment.
  • Detection of Pathogenic Mutations: Obtain information on the potential presence of genetic mutations related to hundreds of diseases, allowing you to take appropriate preventive or follow-up measures.

What Do Genetic Predispositions Mean? Genetic predispositions refer to an increased risk for certain diseases or health conditions due to specific variations in your genes. These variations can influence the likelihood of developing conditions such as diabetes, cardiovascular diseases, or rare genetic disorders. By analyzing your genes, we can identify these predispositions and provide you with information on potential risks you may face. This knowledge allows for tailored preventive measures, better health management, and preparation to address these risks effectively.

What to Expect from Our Test: Our Genetic Predispositions test provides a detailed assessment of your vulnerability index for various genetic diseases. You will learn if you are more predisposed than the majority of the population to develop specific conditions, enabling you to make informed decisions about your health.

Adnà offers you a clear and in-depth view of your genetic predispositions, helping you to better understand and manage your long-term health. Order today for a comprehensive and personalized analysis of your genetic predispositions.

Process

The process for this test is simple:

  • After ordering your test and receiving your collection kit, follow the detailed instructions for collecting your saliva sample.
  • Register your kit and your personal information on the Adnà portal.
  • Return your sample to the laboratory, in its original envelope, for sequencing and analysis.
  • You will be notified by e-mail that your report has arrived in your customer portal on Adnà's website.

Warning

It is important to note that this test should not be used as a clinical diagnostic tool. The information in the report enables you to compare your genetic predisposition with that of the rest of the population. In no way does it indicate whether or not you will suffer from any particular disease. It's important to bear in mind that complex diseases are influenced by many factors: genetic factors are only part of it, lifestyle, diet, etc. also have an influence Any medical concerns or decisions concerning your health should be discussed with a qualified health professional.

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If my report shows a genetic predisposition to a disease, does that mean I'll definitely develop it?

A genetic predisposition to a disease does not guarantee you will develop it. It simply means you have a higher likelihood of developing the condition compared to others, but many people with such predispositions never experience the disease. Genetics is just one factor in your overall health, which is also influenced by lifestyle, environment, and other factors. For a full understanding of your health risks, it's important to consult with healthcare professionals.

Should I change my health habits based on this report?

Before making any health-related decisions or changes, it's crucial to discuss your report with a geneticist or a healthcare professional. They can provide guidance tailored to your genetic information and overall health context.

Do my genes determine everything about my health?

While genes play a significant role, they're just one piece of the puzzle. Lifestyle factors such as diet, exercise, and environmental exposures also significantly impact your health. The goal of this report is to give you more information to manage your health proactively.

What is the foundation of this report?

This report is grounded in globally recognized genetic studies and databases, reflecting a consensus within the scientific community. We apply these studies to your genetic data to provide personalized insights. Each section cites specific studies that support our analysis.

If the report finds genetic mutations associated with a disease, does that confirm I have the disease?

Detecting a mutation does not automatically mean you have the disease. Our report identifies both known pathogenic mutations and those that could potentially lead to disease. It's essential to discuss these findings with a healthcare professional for accurate interpretation.

If no mutations are found for a specific disease, am I completely risk-free?

Our analysis does not cover all possible genetic areas where mutations could occur, and we focus on markers reported as pathogenic. Not finding a mutation doesn't guarantee you're free from the disease, as our test doesn't provide full coverage of all markers. For comprehensive evaluation, consult with healthcare experts.

How does being a carrier of a hereditary disease mutation affect my children?

Being a carrier does not necessarily mean your child will inherit the disease, but it does increase the risk, depending on the inheritance pattern and whether the other parent is also a carrier or affected. Genetic counseling is recommended for carrier testing and to better understand the risks for your family.

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