Reading results

How the heck do I interpret my raw data? I cannot afford to pay a practitioner $$$$$$$$$$ to have these interpreted. I just spent $20 for this and would like to know what is going on with my genetics.

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There are roughly 4 to 5 million SNPs in a person’s genome. Even though only some nominal percentage of that is covered in the processed DNA raw data, it’s an enormous number. Further, given the complexity of gene-gene interactions, you must understand that there isn’t a simple means of “interpreting” your data. The Livewello standard variance report is a good starting place for giving some hints, especially if you’re looking for genetic information related to some health condition; but it is ONLY a start.
I’m afraid that one must either “dig in” and read! There is a fair amount of information pertinent to …the genes and gene SNPs processed in your data. Livewello includes extracts from GWAS (Genome-Wide studies), and links to SNPedia, for example. is another place you can upload your raw data, and you can then download a pc-run program to report by disease condition, gene, etc. …and I often use Promethease side-by-side w. Livewello.
There is also a fair amount of information from research on both gene associations / risks, etc. that is readily accessible online.
But one must do the work or pay experts to do it for you.

It’s best to find a practitioner who is trained in interpreting your raw data for many reasons. When I first learned about mutations from my own 23andMe, I was fascinated and excited to learn more. That’s why a couple of years ago, I completed Ben Lynch’s courses to become certified in Nutrigenomics and add this service to my online Holistic Health practice. I continue to take more of his courses to this day because with genetics being a growing field, we are learning more and more as time goes on. It can be tricky and confusing trying to understand what everything means, and attempting to supplement yourself without proper knowledge can actually end up making some of your symptoms worse.

A good practitioner is someone who will explain your polymorphisms in an easily understandable way, look at your current state of health, (diagnosis’s/ symptoms) as well as your combination of mutations in order to ensure that the protocol they recommend to you contains the right forms and amounts.

Every body is different, which is why something that works for someone else may not work for you; hence the importance of an actual person taking into consideration the entire picture of your health before providing you with recommendations.

I understand your concern about not wanting to shell out a lot more money to have your results interpreted. I’m not sure what prices you’ve come across, but I invite you to check out Elevated Health Solutions. It’s online-based, so the price for Genetic Interpretation Reports & a Recommended Protocol is significantly lower than that of seeing a practitioner in their office.

Otherwise, as far as learning more about this yourself, I would definitely recommend taking Ben Lynch’s courses at Seeking Health Educational Institute.