One Test… a Lifetime of Health
Every GeneSavvy Starter Kit includes whole exome and whole mitochondrial genome data which provides information on over 20,000 genes and over 30,000,000 base pairs. This data set can be utilized in an endless amount of health analysis tools throughout your life.
Once we have your base set of genetic data from the GeneSavvy Starter Kit, we can run it through the analysis tools we’ve built so you can learn how the data plays into your health.
Because the GeneSavvy Starter Kit provides such a massive amount of genetic information, there is plenty of information to explore and research further.
The data provided by our GeneSavvy Testing becomes more valuable every day as new research comes out about the genetic information it contains. We will continue to build new reports and update our health association databases so you can continue to get value out of your GeneSavvy genetic testing data for many years to come!
How It Works?
Purchase your kit online.
Get started with us in just a few minutes! Purchase your GeneSavvy Starter Kit online, it’s fast, simple, and we’ll ship the kit right to your home.
Provide a saliva sample.
We will send a saliva collection kit straight to your house for an easy, comfortable collection process. Provide the sample and drop it back in the mail, it’s as simple as that! Your kit will go directly to our lab for processing after that.
Cant spit in a tube? We can provide options for assisted collection or alternative collection processes. Please contact us to get more information.
Receive your results online.
It takes about 10-14 weeks to process your genetic data. Once the data is in, we will provide online access to the results for you and your health team to get started.
Work with your provider to create a personalized plan of action.
We provide the tools necessary for easy sharing, communication and plan building by your health team. Create action, set goals, and move forward towards more vibrant health using your new GeneSavvy genetic data!
Why Get Tested?
- Percent of Clinically Relevant Mutations Covered by GeneSavvy - 99.9%
Coverage Of Clinically Relevant Gene Mutations (Listed in ClinVar Database)
Outstanding Amounts of Information!
GeneSavvy’s genetic sequencing process was designed to provide information on all possible genes that could be contributing to your health. Our testing produces a massive amount of genetic data that is processed by our own powerful bioinformatics tools to provide with the most actionable data in functional genetics!
Just to give you a visual example of how much data we look at through our testing process; If each base-pair was represented by a penny, we would have enough pennies to wrap around the Earth over 41 times! (Approx. 217,000 miles).
We’ve even gone beyond the standard human exome regions and boosted coverage in disease causing genetic regions to provide your physician an incredible amount of clinically relevant data for the development of targeted action protocols.
Massive Coverage for Better Gene Function Prediction
GeneSavvy testing is designed to provide more comprehensive coverage of the genes you want to know about. This provides the biggest picture possible on the most relevant genes to your current health concerns.
GeneSavvy Genetic Testing provides comprehensive coverage on all genes shown to be relevant in ALL health concerns! If something pops up down the road, we will already have the clinically relevant genetic data for you to take action with without the need for further genetic testing.
Base-Pair Coverage Comparison
Current Treatment Options Need Extreme Personalization!
There are no current FDA approved treatments for Chronic Fatigue Syndrome or Myalgic Encephalomyelitis. The CDC also acknowledges that the treatment of these diseases is extremely complex due to the unknown information about what causes the symptoms. These factors have created the need for extremely personalized treatment approaches that change often based on current and most prevalent symptoms.
When it comes to looking for cause of symptoms to create extremely personalized treatments, genetics are one of the most valuable tools you can use. Looking at genetics can help health professionals find abnormal gene products, biological pathway inefficiencies, and gene/environment actions that can greatly affect the severity of associated symptoms. These factors create a powerful tool for personalized treatments related to Chronic Fatigue and will also hugely contribute to our knowledge of the cause of these complex diseases and assist in diagnosis protocols.
- Amount of genetic research growth
- Investment value increases as fast as research grows
Value of Your Genetic Data
The GeneSavvy Bio-Informatic Process
Annotation Databases Used
We use a large amount of 3rd party databases along with our own databases to create useful data related to your variants! Here are some of the data sources you will find in our reports:
- 1000 Genome Project
- Plus More!
Results You Can Trust
Exome Region Coverage: 50x
Mitochondrial Genome coverage: 500x
GeneSavvy processes your genetic information using state-of-the-art lab equipment and advanced management protocols to ensure the best and most reliable results we can deliver. Our GeneSavvy Genetic testing sequences your genetic exome regions with an average coverage of 50x and your whole mitochondrial genome with an average coverage of 500x.
At GeneSavvy we have developed several proprietary tools that are incorporated in this process to create our full TriarKK™ bioinformatic pipeline.
Treatment Modalities Combined
At GeneSavvy our advisors, panel curators, and treatment option experts have come together from all different modalities of the health industry to provide well rounded treatment options without bias towards one or the other, its all about providing the best action for you. Specialties include:
- Medical Doctors
- Functional Medicine Practitioners
- Naturopathic Doctors
- Doctors of Osteopathic Medicine
- Genetic Counselors
- Nutritionists and Other Functional Health Professionals.