Have you extracted any actionable, effective and yet counter-intuitive (to conventional wisdom and general paleo knowledge) conclusions from 23andme or other genetic testing companies?
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I found out I'm supposedly a "slow metabolizer" of caffeine from 23andme (and so is my father) which means it might increase my risk for heart disease and that generally I don't tolerate it so well. I love coffee, but have known for years that it's problematic for me, so now instead of trying to live with it and drink it for its various purported health benefits, I am careful about avoiding it or carefully controlling the amounts I allow. |
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You probably are not looking for grounds upon which to sue 23andme, but... The word "actionable" means "affording grounds for legal action" and "violating principles of justice." I get that you mean something closer to: "Based on one's genome, what behaviors should one adopt." One thought. If your genetic tests reveal you are a carrier for genes related to, say, cystic fibrosis, you may want to avoid procreating with another human who is likewise a carrier, because two parents with that gene create a far greater chance of producing a child with cystic fibrosis. Otherwise, the main fact remains: Genetic testing reveals risk percentage. Follow a low inflammation lifestyle, eat real food and work up a sweat several times per week. Do what you love. |
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I found out that I am homozygous for the defective form of the MTHFR enzyme, meaning that my body is a very poor metabolizer of folate. I've read some studies that have linked this to mental health issues. I've had schizophrenia since I was 13. Most mental health professionals give very little focus to diet in the treatment of mental illness. I wonder how well I would have responded to diet changes when I was 13 instead of riding the psychiatric medication merry-go-round. I am not criticizing mental health professioanals by any means because there is very little research into the relationship between diet and mental health. Still, it would be nice if I didn't have to deal with the side effects of the medications I've been on. |
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I have found out that I'm a little bit more neanderthal than John Durant ;). I also supposedly have a low risk of obesity (as if). So for me, not so much in the area of actionable findings (yet). |
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I found out I have the genes for "hemochromatosis". Yet I have been severely anemic my whole life. I guess those genes just haven't been expressed. |
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I don't know, I work a lot in the field of breast cancer, and I know that the BRCA tests on the 23andme or similar home genetics test are not done with proper scientific process (this is per the oncologists I work with). So I probably wouldn't trust these results in general much. |
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Woah, I just got my results and there's one that has me stumped. It seems I may respond poorly to high levels of saturated fat in my diet. Does anyone else have this in their report (for the APOA2 gene)? http://www.snpedia.com/index.php/Rs5082(C;C) I'm not quite sure what to make of this. I guess I'll try a lower-fat diet for a while and see if I notice any fat loss? I haven't been losing weight on paleo, so maybe that's why? Edited to add: Actually, 23andMe has turned out to be super important. Despite a gluten free diet for over a year, I'm still suffering symptoms from celiac disease, especially mood, energy, and mental problems. I found out I am heterozygous for a MTHFR mutation, as well as homozygous for a COMT mutation. Taking folate, methylcobalamin, and SAM-e has been very helpful. I also have a Leiden factor II mutation, which further complicates homocysteine blood clotting problems. It continues to be a scavenger hunt to piece things together, but the SNP analysis has been invaluable. |
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I highly recommend checking out Promethease: http://www.snpedia.com/index.php/Promethease It takes your raw 23andme data and gives you much more info with useful suggestions. |
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The only information I found relevant to my diet is that I have a genetic predisposition towards lactose intolerance. I emphasize 'predisposition' because they mention that certain environmental factors can affect this. Sadly, they don't list them or refer to any clinical studies though. |
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