Detox and Methylation Mutation Report for Customer: a-97dd-6604ce662da3

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NutraHacker Detox and Methylation Mutation Report for Customer: 71666422-3218-464a-97dd-6604ce662da3 Instructions: This FREE NutraHacker report contains detox and methylation mutations (single nucleotide polymorphisms) in this uploaded genome. Genes not reported in this report are either normal, not actionable, available only in the paid service offered by NutraHacker, or are not currently detected by NutraHacker. The expected allele is the one seen in a normally functioning gene. The high risk alleles reported are the ones measured from the uploaded genome. NutraHacker reports the effects of these mutations as discovered by published empirical data and suggests nutritional supplements that can mitigate potential issues caused by these mutations. This report is meant to serve as a guide for nutritional supplementation for the owner of the genome and is not applicable to any other individual. Supplement quantities and dosages are not included as they are indicated on the purchased product. Multiple recommendations for the same supplement does not mean that the dosage should be multiplied. In the case of a conflict (such as a particular vitamin being both encouraged and discouraged), the owner of the genome should assess his/her own personal biology to decide whether to include or discard that particular supplement. NOTICE: State law allows any person to provide nutritional advice or give advice concerning proper nutrition--which is the giving of advice as to the role of food and food ingredients, including dietary supplements. This state law does NOT confer authority to practice medicine or to undertake the diagnosis, prevention, treatment, or cure of any disease, pain, deformity, injury, or physical or mental condition and specifically does not authorize any person other than one who is a licensed health practitioner to state that any product might cure any disease, disorder, or condition. NutraHacker reports are for scientific, educational and nutritional information only and are not intended to diagnose, cure, treat or prevent any disease, disorder or condition. Thank you for using NutraHacker. To your health! Gender of customer: Female A total of 18 mutations were detected at this time for your genome out of the 58 polymorphisms assessed. There were 8 homozygous mutations.

There were 10 heterozygous mutations. Please continue to the next page to begin your discovery process.

Detoxification rs1799814 CYP1A1 G GT: 1/2 7.19400% Phase I xenobiotic metabolism, Reduced function of enzyme Diindolylmethane PAH's, metabolize E2 to 2-hydroxyestradiol Detoxification rs762551 CYP1A2 A AC: 1/2 46.8902% Hydroxylation or dealkylation of xenobiotics, Phase I, metabolize E2 to 2-hydroxyestradiol Slow to metabolize caffeine, Main liver pathway Induce with broccoli, Cabbage, Diindolylmethane, Glucarate, NAC, Cardamom, Sulforaphane Detoxification rs1800440 CYP1B1 A CT: 1/2 21.5369% 4-hydroxylation of estrogen Probable increased enzyme Diindolylmethane function, increased deleterious estrogen metabolism and activation of pro-carcinogens Detoxification rs1065852 CYP2D6 C AG: 1/2 30.2957% Detoxifies 20% of prescription Poor metabolizer drugs Detoxification rs1695 GSTP1 G AG: 1/2 42.4696% Conjugation toxins to glutathione Persons having the alleles AA or NAC, Whey AG had an increase in inflammatory interleukin-6 (IL-6) upon supplementing alpha-tocopherol (the most common form of Vitamin E in a North American diet) while those with GG saw a decrease. Detoxification rs1208 NAT2 A GG: 2/2 14.6514% This gene encodes an enzyme Fast metabolizer NAC, Vitamin B2, that functions to both activate and Vitamin B3, Vitamin deactivate arylamine and B5, Molybdenum hydrazine drugs and carcinogens. Detoxification rs1801280 NAT2 T CC: 2/2 13.1072% This gene encodes an enzyme Decreased activity NAC, Vitamin B2, that functions to both activate and Vitamin B3, Vitamin deactivate arylamine and B5, Molybdenum hydrazine drugs and carcinogens. Neurotransmitter rs4633 COMT C CT: 1/2 48.7173% Degrades catecholamines, Phase Same amino acid sequence, Hydroxy B12 II, inactivates hydroxy-estrogens lower expression of gene, less (hydroxycobalamin) breakdown of catecholamines Curcumin, Cumin, Grapefruit Substrates of this enzyme Vitamin E Methyl B12, Methyl donors

Neurotransmitter Neurotransmitter rs4680 COMT G AG: 1/2 48.2074% Degrades catecholamines, Phase II, inactivates hydroxy-estrogens rs6323 MAO-A G TT: 2/2 N/A Oxidizes serotonin, dopamine, epinephrine, norepinephrine rs651852 BHMT08 T CT: 1/2 48.0752% Methylates homocysteine to methionine rs234706 CBS G AG: 1/2 39.9436% Adds l-serine to homocysteine to produce l-cystathionine rs1805087 MTR A GG: 2/2 4.79560% Converts homocysteine into methionine Slower breakdown dopamine, Hydroxy B12 oestrogen, worrier, prone to (hydroxycobalamin) anxiety, more sensitive to green tea Methyl B12, Methyl donors, Cannabis Lower expression of MAO A Progesterone Curcumin, Estrogens, Androgens Downregulation Phosphatidylcholine, TMG, Phosphatidylserine, Zinc Increased responsiveness to Vitamin B6 homocysteine-lowering effects of folic acid. Marginally increased disposal of homocysteine. Upregulation that can deplete Methyl b12, methyl-b12. L-methylfolate, Lithium orotate, Grapeseed extract rs1802059 MTRR G AA: 2/2 9.58110% Methylates, recycles vitamin b12 Less active enzyme Methyl B12 rs1801394 MTRR A AG: 1/2 49.3785% Methylates, recycles vitamin b12 Poor methylation of Vitamin B12 Methyl B12, leading to higher homocysteine L-methylfolate levels. HPA axis / Endocrine rs1544410 VDR G TT: 2/2 9.58600% Vitamin D Receptor Downregulated Vitamin D Vitamin D3, Sage, Methyl donors receptor Rosemary HPA axis / Endocrine rs731236 VDR A GG: 2/2 10.0873% Vitamin D Receptor Downregulated Vitamin D receptor, can affect dopamine levels Vitamin D3, Sage, Rosemary Methyl donors

Energy / Oxidation rs4880 SOD2 A GG: 2/2 18.1693% Mitochondrial Superoxide Decreased gene function. Noise Manganese, Vitamin Alcohol, Noise Dismutase 2 induced hearing loss, rs10370 E in tocotrienol form (greater chance for 'TT', rs4880 'GG' diplo-genotype hearing loss) (diplotype) was associated with more gray matter shrinkage in 76 individuals who report chronic high levels of alcohol consumption.