NutraHacker FAQ

Question: Why do I sometimes see conflicting supplement recommendations and how should I interpret them?

Answer: It is common to see some supplements both recommended as well as cautioned against. Conflicts happen because our software looks at each rsID
individually and makes a recommendation just for that particular polymorphism. The human body is very complex and can have both positive and
negative reactions to different compounds. Each conflict needs to be assessed on a personal basis--possibly the correct course of action will be
apparent from the biochemistry of the genes involved, or you may need to rely on trial-and-error. Two examples that appear often are curcumin and methyl-B12.

Curcumin is a fascinating compound with many effects on the body. It has liver-protective effects, can be used to stimulate poorly functioning
detoxification genes, and is neuroprotective. However, it inhibits MAO-A which can have negative effects on brain biochemistry, especially if you have
a low-functioning form of MAO-A. In this case you might want to try curcumin for its health benefits but drop it if side-effects are noticeable.

If methyl-B12 is recommended as the optimal form of B12 but you have an adverse reaction to methyl donors, then hydroxy-B12 is probably a better
choice. Some polymorphisms in COMT cause the enzyme to function at a decreased rate, which allows methyl-donating compounds to accumulate.

In general, NutraHacker supplement recommendations are meant to serve as a guideline or starting point for pinpointed health supplementation using your
own genetics. Some conflicts are unavoidable, but that is because we are giving you the most in-depth look into your own personal genetics available to date!

Question: My report says to avoid methyl donors. Could you please tell me what a methyl donor is?

Answer: A methyl donor is a molecule that has an available methyl group (-CH3) for reaction in the body. Methyl groups might be used to
activate/inactivate compounds in the body, and affect things like liver detoxification, histamine, levels of brain neurotransmitters,
and DNA expression. A couple examples of methyl donors as supplements are trimethylglycine, SAM-e, and methylcobalamin.


Question: Why is dosage information for supplements not included in my report?

Answer: NutraHacker does not give dosage information for supplementation. This information is included on the supplement bottles which can vary depending on the form of the supplement and goals desired.

Question: Why don't you analyze mitochondrial snps like NDUFS8?

Answer: Due to the threshold effect, mitochondria don't typically show negative health effects until 25% of the mitochondrial genome is mutated (http://www.ncbi.nlm.nih.gov/pubmed/12467494). We have many mitochondria per cell and they have a high mutation rate so while snp analysis in mitochondria is useful for geographic and historical analysis, we feel analysis for overall health purposes has limited benefits.

Question: What do "RSID","Expected","Genotype", "Risk" and "Genotype Frequency" mean?

RSID: Rapid Stain Identification Series (this number denotes a unique polymorphism in the genome, think of it as the 'address' where you look up the alleles you are interested in).

EXPECTED: This is the more beneficial version of a polymorphism. Usually this is the more common type, but sometimes the less prevalent version actually has a better function.

GENOTYPE: Your actual alleles compared to the expected. Since we have two copies of genes, you get two alleles- unless you are a male and the gene is on the Y chromosome.

RISK: The deviation from expected. Yellow (1/2), also known as heterozygous, means you have one 'normal' copy of an allele and one altered version. Red (2/2 or 1/1) is homozygous meaning no 'normal' copy exists. These of course are more serious!

GENOTYPE FREQUENCY: The prevalence of your genotype, or combination of alleles, in the population. It's interesting to compare and see how many others are like you, isn't it?


Question: I don't quite understand what the Celiac report is saying. I believe it's telling me that I don't have the genes for Celiac disease. However, I am gluten sensitive as is my entire family. Is there anything in this report that alludes to that?

Answer: That is correct, this report is just for the chance of Celiac which in this case is unlikely. It doesn't cover other causes for gluten sensitivity. Please see Celiac.org for more info regarding gluten sensitivity.

Question: How do I use the Depression Report? What are the predictions?

Answer: Think of this report as more of a tool than something which spells out exactly what you should do. The first suggestion is to pull
up the dynamic graphs (the bar charts), select your ethnicity, and then select "All treatments with predictions." The predictions are
used to make a judgement call when your variant is heterozygous. From the formed chart, you look for meds which have the
highest green bar to lowest red bar (green is a gene with a positive response and red is a decreased response). You will have a
few that pop up as good options, and you can look overall at what classes those are in, and if they are in different classes you can
decide which class of antidepressant looks good.

If you want to get into the research, or are working with a doctor who wants to see it, you can bring up the dynamic table and
search by any variable you want, such as for the specific med. That will bring up the data, responses, and research so you can see
how the information was collected.


Question: How can I upload my data if I do not remember my 23andMe login, or if I have Ancestry data?

Answer: Please use the raw text file upload option.

Question: How do I download my Ancestry raw data?

Answer: For step-by-step instructions from Ancestry.com please click here.

Question: How do I purchase all available complete products?

Answer: Please get started by clicking either on the button below:


or upload your raw 23andMe file.

After filling out the questionnaire, you will be able to purchase all available products.


Question: I already uploaded my data and answered the questionnaire, but lost my report links. How do I access my reports?

Answer: Please use the report center.

Question: Do you process data from Genes for Good?

Answer: The data from Genes for Good does not have enough overlap with our system so we do not process this data source.

Question: What does it mean to "whitelist" sales at nutrahacker dot com?

Answer: To "whitelist" an email address is to specifiy explicitly that you want to receive email from that address.
See how to setup a "whitelist" in Gmail.




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