Genome It All
A Splice of Your Life!
Genome It All wants to ensure you have a thorough look into your genes to ensure you have enough information to make the right choices for YOU!
We do not just include information on a few important Single nucleotide polymorphisms (SNPs), but THOUSANDS of them, so you can see the whole picture. And we charge the same or less than our competitors who offer much less!
With Genome It All, You won't have to read to endless studies and try to interpret them, we have already done that for you! We personally have researched and narrowed down the studies of over 30,000 SNPs that are included on our genotype report.
We also provide natural suggestions based off the results, if applicable.
Order Your Genome It All Test Kit Now!
For only $349.00 you get 5 different files with your genetic testing:
We will mail you a testing kit that uses a simple swab system, which is easy to use on infants or adults.
Then return your kit to our certified lab and once your sample is completed, we will send:
You heard it right! Not only will you get a raw data file of your ~700,000 SNPs, you will also get a customized report on over 30,000 SNPs that have each been individually researched and broken down so that the results are easy to understand. We do not use a computer system to auto-generate results from a web based program that is available to the public. We have built our "Genome It All" report exclusively for our customers only!
Our service also includes a break down report on: Vitamin Metabolism, Methylation, Detoxification and Autoimmune Susceptibilities. This report will help to tell you which forms of certain vitamins should work best for you based on your genetic results. It can also tell you if you have reduced detoxification in your environment and lifestyle.
Heath Associations Report
We include an additional report that will highlight any carrier or pathogenic findings so that you can see any findings that might need immediate attention.
You can get a review of your Genome It All Testing for $269.00. With this service, we will ask that you fill out a health intake form. We will then review your concerns and narrow down your Genome It All results based on those concerns.
We provide a report that will show you the totals of results on each category and gene on your report.
You will receive a raw data file with ~700,000 SNPs included.
If you have been searching for answers to your health and lifestyle concerns and still need answers, then you have come to the right place!
We ensure your privacy and will not share or sell your data!
Purchases in the United States: Shipping is included in the purchase price, which also includes return shipping to get your samples back to our lab.
Purchases outside of the United States: Shipping is included in the purchase price to get our sample kit to you, however, return shipping to get your samples back to our lab is NOT included as this typically requires a customs form to be completed.
We are currently running the latest generation GSA v3 chip from Illumina.
Turn around time
Once we receive your results at our lab, there is a 3 to 4 (30 business days) week turn-around time.
You will receive all 5 files/reports at the same time via the email address you provided with your purchase.
If you have any problems or concerns, or you believe it has been past the 3-4 week time frame, please contact us.
COVID-19: Our lab is currently testing for COVID-19, which can delay reporting an additional week.
Use the checkout tool to securely pay, and order your kit today!
See a Full List along with Description Below.
What you can expect to see on your report:
Allergies- Susceptibilities, triggers
Bugs, Dust mites, Food, Gluten, Lactose, Seasonal
Aging- Susceptibilities, Traits on aging, Longevity
Amino Acids- Changes, Deficiencies, Breakdown abilities
2-aminobutyrate (AABA), Alanine (Ala), Arginine (Arg), Citrulline (Cit), Creatine (CK), Cysteine (Cys), Glutaric aciduria, Glutamine (Glu), Glycine (Gly), Isobutyryl-CoA dehydrogenase (IBD), Isoleucine (Ile), Acetyl L-Carnitine (LCT), Leucine (Leu), Lysine (Lys), Methionine (Met), Ornithine, Proline (Pro), Serine, Tryptophan, Tyrosine, Valine (Val).
Antibody- Response, Susceptibilities
Antineutrophil Cytoplasmic Antibodies (ANCA), Cytokines, Duffy, Insulin-like Growth Factor, Neutrophils, Immunoglobulin: A, D, E, G.
Antioxidant- Abilities, Cellular, Production, Recycling
COQ10, Glutathione, Indole propionic
Athletic Potential- Muscle types, Response to fitness, Aerobic capacity, Endurance, Strength.
Angiotensin, Metabolic Equivalent Task (MET), VO2 Max.
Glycogen storage disease.
Autoimmune -Reactions, Risks, Susceptibilities
Interleukin-6 (ILG), Tumor Necrosis Factor (TNF)
Arteriosclerosis, Bechet's, Myasthenia Gravis, Multiple sclerosis, Pediatric, Rheumatoid arthritis, Sjogren's, Systemic lupus erythematosus, Systemic sclerosis
Birth defects- Risks, Carrier status
Conotruncal Heart Defects, Microcephaly, Neural tube defects (NTDs), Smith-Lemli-Opitz syndrome.
Blood- Types, Changes, Risks, Coagulation.
Albumin, Antithrombotic, Citrate, Complement C3, D-dimer, Ferritin, Fibrin, Hematocrit, Hemoglobin, Mean Corpuscular Hemoglobin (MCH), Mean corpuscular volume (MCV), Plasminogen, Platelet, Porphyrin, Pressure, Proteins, Prothrombin, Thromboplastin.
Beta thalassemia, Factor IX deficiency disease (Hemophilia B), Factor V, Upshaw-Schulman syndrome (USS), Von Willebrand factor (VWF), X-linked sideroblastic anemia.
Blood Pressure- Preeclampsia, Sensitivities, Risks, Heritable Traits
Diastolic, Mean Arterial, Systolic, Pulse/heart rate.
Brain- Activity, Changes, Development, Structure, Risks, Traits, Volume
Amygdala, Atrophy, Carotid intima media thickness, Cerebral cortex, Cerebrospinal fluid (CSF), Entorhinal cortex, Grey Matter, Hippocampus, White Matter.
Aicardi-goutieres syndrome, Aneurysm, Cerebral infarction, Congenital muscular dystrophy, Craniopharyngioma, Encephalopathy, Glioma, Heterotopia, Hereditary diffuse leukoencephalopathy with spheroids, Hippocampal sclerosis of aging, Holoprosencephaly, Intracerebral hemorrhage, Lissencephaly, Palsy, Pigmented nodular adrenocortical disease, Polymicrogyria, Scaphocephaly, Traumatic brain injury (TBI), X-linked adrenoleukodystrophy.
Cancer- Risks, Susceptibilities, Traits, Toxin exposure changes, Benefits
Basal, Bladder, Blood, Brain, Digestive, Kidney, Lung, Mouth, Neoplasm, Thyroid.
Adenoma, B-Cell Non-Hodgkin Lymphoma, Bloom syndrome, Breast, Chronic myelomonocytic leukemia (CMML), Endocrine, Endometrial, Esophageal squamous-cell carcinomas, Ewing sarcoma, Familial adenomatous polyposis, Follicular lymphoma, Gallbladder, Glioma, Glioblastoma, Hamartoma, Hereditary hemorrhagic telangiectasia, Juvenile polyposis syndrome, Leukemia, Lymphoma, Lynch Syndrome, Melanoma, Meningioma, Mesothelioma, Multiple endocrine neoplasia, Myeloma, Myeloproliferative Neoplasms, Nasopharyngeal carcinoma, Neuroblastoma, Neurofibromatosis, Non-hodgkins Lymphoma, Non-small cell lung cancer, Pancreatic cancer, Prostate cancer, Renal cell carcinoma, Retinoblastoma, Sarcoma, Squamous cell carcinoma, Squamous intraepithelial neoplasia.
Cardiovascular -Health, Risks, Traits, Susceptibilities
Arrhythmia, Atrial septal defect, Brain natriuretic peptide (BNP), Electrocardiogram (ECG), PR interval, QRS wave, QT interval, Rate, Rhythm.
Acute coronary syndrome, Acute myocardial infarction, Atrial fibrillation, Becker muscular dystrophy (BMD), Brugada syndrome (BS), Cantú syndrome, Cardiac arrest, Congestive heart failure, Coronary calcification, Duchenne muscular dystrophy, Hypertension, Hypertrophic cardiomyopathy, Long QT syndrome, Myocardial infarction, Tachycardia, Ventricular septal defect.
Cells -cellular damage by free radicals, cell traits/variations.
B lymphocyte, Fetal hemoglobin, Kupffer, Leydig, Macrophages, T lymphocytes, Red blood cells, White blood cells/ Eosinophil.
Graft-versus-host disease, Niemann Pick Disease C1, Sarcoidosis, Sickle, Stem.
Benzalkonium chloride, Ethanol, Phosphate, Polyvinyl chloride, Trimethylamine
Cholesterol- Build up potential, Traits, Risks
High-density lipoprotein (HDL), Lecithin-cholesterol acyltransferase (LCAT), Low-density lipoprotein (LDL), Total, Triglycerides.
Chromosomes- Abnormalities, Structure and Function
Telomeres, Y chromosome.
Nijmegen breakage syndrome (NBS).
Defects -Skeletal, Developmental, Risks, Carrier status
Cleft Lip Palate, Contruncal heart defects, Frontonasal dysplasia, Hypospadias, Morphology, Tetralogy of fallot, Ventricular septal defect (VSD)
Acetyl-CoA acetyltransferase, Adenylosuccinate lyase, Argininosuccinate lyase deficiency, Aromatase, Biotinidase, Tetrahydrobiopterin, Glutaric aciduria, Methylmalonyl-CoA epimerase deficiency, Phosphorylation, Short-chain acyl-CoA dehydrogenase.
Degeneration- Degenerative disc disease, Risks
Alzheimer’s Disease, Frontotemporal, Lewy body disease.
Dental- Susceptibilities, Deficiencies
Agenesis, Caries, Gums, Enamel.
Odontogenesis, Periodontitis, Temporomandibular joint dysfunction
Development- Growth, Height
Idiopathic short stature, Small for gestational age
Developmental disorder- Risks, Carrier status
Adolescent idiopathic scoliosis, Arthrogryposis multiplex congenita, Asperger's, Autism, Bardet-Biedl syndrome, Beckwith-Wiedemann syndrome, Cornelia de Lange syndrome, CHARGE syndrome, Charcot-Marie-Tooth disease, Chondrodysplasia, Cockayne syndrome, Coffin-Siris syndrome, Costello syndrome, Crouzon syndrome, Geleophysic dysplasia, Hemophagocytic lymphohistiocytosis, Kallmann syndrome, Lethal congenital contracture syndrome, Limb-girdle muscular dystrophy, Levy-Hollister syndrome, Multiple congenital anomalies-hypotonia-seizures syndrome, Metaphyseal dysplasia, Spahr type, McKusick Kaufman syndrome, Microcephaly, Microphthalmia, Mucolipidosis, Mucopolysaccharidosis, Mowat-Wilson, N-terminal acetyltransferase deficiency, Multiple congenital anomalies-hypotonia-seizures syndrome (MCAHS), Myhre syndrome, N-terminal acetyltransferase deficiency, Osteoglophonic dysplasia, Pfeiffer syndrome, Phosphoglycerate dehydrogenase deficiency, Pitt-Hopkins syndrome, Roberts-SC phocomelia syndrome, Rett syndrome, Rhizomelic chondrodysplasia punctata, Roberts-SC phocomelia syndrome, Rubinstein-Taybi syndrome, SHORT syndrome, Spondyloepimetaphyseal dysplasia Missouri type, Smith-Kingsmore syndrome, Seckel syndrome, Tatton-Brown-rahman syndrome, Tay-Sachs disease, Visceral heterotaxy.
Additives, Bitter, Carbs.
Asparagus, Sodium, Sugar, Vegetables.
Digestive- Food sensitivities, Digestive problems, Risks
Crohn’s disease, Dysbiosis, Gastroesophageal reflux disease, Gastritis, Helicobacter pylori, Hereditary fructosuria, Hypochlorhydria, Intestinal atresia, Irritable Bowel disease, Microbiota, Pancreatitis, Parasitic Infections, Slow transit constipation, Stomach acid, Ulcerative Colitis
Disorders- Developments, Mental, Growing, Aging, Risks, Carrier status
Dystonia, Eating, Hair, Migraine, Movement, Neuromuscular.
Bardet–Biedl syndrome, Brachydactyly, Congenital ichthyosis, Cutis laxa, Creutzfeldt-Jakob disease, Congenital adrenal hyperplasia, Congenital disorder of glycosylation, Congenital disorder of glycosylation type, Coffin-Siris syndrome, Costello syndrome, Diffuse mesangial sclerosis, Friedreich's ataxia, Familial dyskinesia with facial myokymia, Glutaric acidemia, Ghosal hematodiaphyseal, Huntington disease, Hermansky-Pudlak, Hirschsprung disease, Joubert syndrome, Limb-girdle muscular dystrophy, dystroglycanopathy, Lipodystrophy, Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome, Methylmalonic acidemia Noonan syndrome, Noonan- like syndrome with loose anagen hair, Papillon-Lefèvre syndrome, Pitt-Hopkins-like syndrome, Pseudoxanthoma elasticum, Reticulosis, Rhizomelic chondrodysplasia punctata, Rubinstein-Taybi syndrome, Spinocerebellar ataxia, Sjogren-Larsson syndrome, Telangiectasia, Tuberous Sclerosis Complex, Von Hippel-Lindau syndrome, Vogt-Koyanagi- Harada Disease, Wolfram.
Elements -Metals, Mineral levels or deficiencies
Copper, Iron, Lead, Mercury, Phosphorus, Sulfur
Environmental- Exposure, Reduced clearance or build up
3-phenylpropionate hydro cinnamate, Aflatoxin B1, Carbon Monoxide, Chemicals, Cigarette smoke, Dioxins, Heterocyclic amines, Levulinate, Pesticides, Phthalates, Pigments, Polychlorinated biphenyls (PCBs), Radiation, Reactive oxygen species
Enzymes- Breakdown, Deficiencies, Risks
Alkaline phosphatase, Arylsulfatase A, Aspartate aminotransferase, Butyrylcholinesterase, Gamma glutamyl transpeptidase, Guanidinoacetate methyltransferase, Lactate Dehydrogenase, Matrix Metalloproteinase, NADPH (nicotinamide adenine dinucleotide phosphate), Phenyllactate, Plasmin, Xanthine.
Exocrine pancreatic insufficiency, Hereditary coproporphyria, Isovaleryl-CoA dehydrogenase deficiency, Glycogen storage disease, Metachromatic leukodystrophy (MLD).
ENT (Ear, nose, throat)- Development, Risks, Carrier status, Smelling ability
Motion, Smell, Tonsil, Vertigo
Rhinosinusitis, Usher syndrome
Eyes -Vision changes/Loss, Carrier status
Axial, Eye dystrophy, Color, Cornea, Cup, Defects, Disc, Optic disc, Pressure, Eye Refraction, Retina, Vision.
Age related macular degeneration, Astigmatism, Bette crystalline corneoretinal dystrophy, Cataracts, Glaucoma, Ocular albinism, Optic atrophy, Nearsightedness (myopia), Retinopathy
Fatty Acids- Aromatic, Metabolism
2-hydroxyisobutyrate/ alpha-hydroxybutyrate, Arachidonic acid (Omega 6), Omega-3, Docosatrienoic acid, Eicosapentaenoic acid, Long-chain fatty acids, Palmitoleic acid, Phenyl acetate, Polyunsaturated fatty acids.
Female- Traits, Risks
Breasts, Disorders, Ovaries
Endometriosis, Fibroids, Ovarian dysgenesis, Ovarian hyperstimulation syndrome, Pelvic organ prolapse, Polycystic ovary syndrome (PCOS)
Genetic- Changes, Carrier status, Expression; DNA repair
Lethal arthrogryposis with anterior horn cell disease
General- Energy/Energy Production
Hearing- Loss, Risks, Carrier status
Hearing Impairment, Otosclerosis, Pili torti.
Hormones- Changes, Susceptibilities, Therapy
Adrenocorticotropic, Androgen, Cortisol, Dehydroepiandrosterone (DHEA), Epinephrine, Gonadotropin, Growth hormone, Leptin, Melatonin, Oestradiol, Oxytocin, Sex hormones.
Immune system- Ability, Reaction, Risks, Immunities
Ataxia, Autoimmune lymphoproliferative syndrome, Common variable immunodeficiency, Granulomas, Graves disease, Hyper IgM, Immunodeficiency, centromeric instability, and facial dysmorphism, Mannose-binding protein deficiency, Major histocompatibility complex, Severe Combined Immune Deficiency
Infant Disorders- Carrier status, Risks
Nervous system, Neurological, Respiratory.
Bifunctional peroxisomal enzyme deficiency, Canavan disease, Congenital amegakaryocytic thrombocytopenia, Ceroid lipofuscinosis neuronal, hypertrophic pyloric stenosis, Infantile hypertrophic pyloric stenosis, GM1-gangliosidosis, Mitochondrial complex III deficiency neonatal diabetes mellitus, NGLY1-congenital disorder of deglycosylation, Non-ketotic hyperglycinemia, Persistent hyperinsulinemic hypoglycemia of infancy, Sudden infant death syndrome, Tyrosinemia, Zellweger syndrome.
Bacteria, Herpes, Leprosy, Septic.
Inflammation- Response to stimuli, Sensitivities, Triggers
Eosinophilic esophagitis (EoE), Erythrocyte sedimentation rate (ESR), Gout, Tumor Necrosis Factor (TNF), TNF receptor-associated periodic fever syndrome.
Insulin- Diabetes, Blood Sugar & Cardiovascular Markers
Fasting, Glucose, Insulin Secretion Index, HOMA-IR (Homeostatic Model Assessment for Insulin Resistance), Resistance, Sensitivity.
Diabetes, Hypoglycemia, Metabolic syndrome, MITCHELL-RILEY SYNDROME (MTCHRS), Type 1 diabetes nephropathy.
Kidney- Disorders, Risks, Defects, Function
Dialysis, Disease, Dysplasia, Filtration, Hematuria, Renin, Renal, Stones, Transplant
Acute Kidney Injury, Aquaporin 1 deficiency, Autosomal recessive distal renal tubular acidosis, Factor H deficiency, End-stage renal disease, Glomerulocystic kidney, Idiopathic membraneous nephropathy, Nephrotic syndrome, Nephropathy, Polycystic kidney disease, Primary hyperoxaluria, Renal Hypomagnesemia
Learning- Abilities, Benefits, Deficiencies, Traits
Dyslexia, Education, Speech
Lifestyle - Preference, Risk
Alcohol, Caffeine, Cannabis, Drugs, Gambling, Smoking,
Lipids- Structure and Function, Traits, Risks/Susceptibilities, Defect, Metabolism
Apolipoprotein, Apolipoprotein A-I (apo A-I), Apolipoprotein A-II (apo A-II), Lipoprotein(a), Phospholipid, Sphingolipid, Sulfatides.
Hyperlipoproteinemia, Sitosterolemia, Very long chain acyl-CoA dehydrogenase deficiency.
Liver- Disorders, Risks, Defects, Function
Bile, Bilirubin, Cholestasis, Cirrhosis, Dysplasia, Hepatocyte growth factor, Hepatotoxicity.
Acute intermittent porphyria, Alkaline phosphatase, Aspartate transaminase, Dubin-Johnson syndrome, Gamma-glutamyl transpeptidase, Gallstones, Hepatitis, Nonalcoholic fatty liver disease, Primary biliary cirrhosis, Primary sclerosing cholangitis.
Male- Traits, Risks
Prostate, Sex steroid.
Mental Capacity- Mental abilities, Traits
Cognitive, IQ, Memory.
ATR-X syndrome, Mental retardation, Mental retardation-hypotonic facies syndrome, Poretti-boltshauser syndrome.
Mental Health - Risks/Susceptibilities
Aging, Neuroticism, Prion.
Attention deficit hyperactivity disorder (ADHD), Bipolar, Conduct Disorder, Obsessive compulsive disorder (OCD), Posttraumatic Stress Disorder (PTSD), Schizophrenia.
Metabolism- Fat & Carbohydrate Metabolism, Vitamins
Carnitine palmitoyltransferase, N-acetylcarnosine, X- 12095- -N1- methyl-3-pyridine-4- carboxamide.
Metabolic Syndrome, Maple syrup urine disease, Niemann-Pick disease.
Methylation- Pathways, Abilities, Deficiencies, Risks/Susceptibilities
CpG islands, Homocysteine.
Minerals- Levels, Absorption, Deficiencies, Reduced clearance, Build up
Calcium, Magnesium, Phosphorus, Potassium, Oxalic acid, Selenium
Mitochondria- Changes, Structure/Function, Risks/Susceptibilities
Adenosine triphosphate, Complex III.
Alpers, Leigh syndrome (LS).
Mood Disorder- Risks/Susceptibilities
Depression, seasonal affective disorder (SAD).
Musculoskeletal- Changes, Structure/Function, Risks/Susceptibilities, Disorders
Anterior cruciate ligament, Adenosine monophosphate deaminase, Lactic acid, Motion, Pain, Tendon, Tissue.
Emery-Dreifuss muscular dystrophy, Ehlers-Danlos syndrome, Fibromyalgia, Intermediate muscular dystrophy, Limb-girdle muscular dystrophy, Muscular atrophy, Muscular dystrophy, Myopathy, Myotonia, Paralysis, Systemic sclerosis.
Nervous system- Nerves, Changes, Structure/Function, Risks/Susceptibilities
Central Nervous system, Myelin, Polyglucosan, Psychomotor, Tumor.
Angelman, Carpal tunnel syndrome, Ceroid lipofuscinosis neuronal, Charcot-Marie-Tooth Neuropathy, Dysautonomia, Encephalopathy, familial, with neuroserpin inclusion bodies, Neuroma, Parkinson's, Salla disease, Spastic paraplegia, Tourettes.
Neurocognition, Neurodegeneration, Neurodevelopmental, Neuropathy, Neuron Disease, Stroke, Tangles, Tremor, Tics.
Amyotrophic lateral sclerosis Acute hepatic porphyria, Alpha-methyl acyl-CoA racemase deficiency, Asparagine Synthetase Deficiency, Carbohydrate-deficient glycoprotein syndrome, Charcot-Marie-Tooth disease, Desmosterolosis, Dihydropyrimidine dehydrogenase deficiency, Epilepsy, Hereditary motor and sensory neuropathy, Mucolipidosis, Parkinson's, Restless legs syndrome (RLS), Seipinopathy, Silver spastic paraplegia syndrome, Temtamy
Neurotransmitter -Brain chemistry balance, Changes
3-Methoxy-4-hydroxyphenylglycol (MHPG), Dopamine, GABA (gamma-aminobutyric acid), Serotonin.
Osteo- Bone Health, Softening, Traits, Breakdown, Carrier Status
Bone Marrow, Bone mineral density (BMD), Broad-band ultrasound attenuation (BUA), Degeneration, Development, Fractures, Ossification, Osteolysis, Sclerosteosis, Scoliosis, Thoracic Spine.
Ankylosing spondylitis, Arthritis, Metachondromatosis, Osteogenesis imperfecta (OI), Osteonecrosis of the femoral head (ONFH), Osteoporosis, Ossification of the posterior longitudinal ligament, Paget’s disease of bone, Spondylometaphyseal dysplasia with cone-rod dystrophy.
Ammonia, Homovanillic acid (HVA).
Cytochrome c oxidase i deficiency.
Agreeableness, Creativity, Leadership, Novelty, Openness, Persistence, Political
Pharmacogenomics- Reactions to medicines, Metabolism, Deficiencies, Reduced breakdown, Build up, Risks
Proteins- Structure/Function, Traits, Changes
Amyloid, β2-glycoprotein I (β2GPI), Complement C4, C-reactive protein (CRP), Collagen, Cystastin C, Galectin-3 (gal3), Glycoprotein, ICAM-1 (Intercellular Adhesion Molecule 1), Monoclonal, myeloperoxidase, Peptides, Perforin, soluble P-selectin, Soluble ST2 (sST2).
monoclonal gammopathy of unknown significance.
Psychological- Traits, Risks, Carrier status, Response to Stress
Anger, Anxiety, Coping, Emotion, Stress, Suicide, Tendency.
Reproduction- Ability to reproduce, Carrier status, Risks
Follicle-stimulating hormone (FSH), Gestation, Persistent organic pollutants (POPs), Placenta, Sperm.
Hypogonadism, Infertility, Menarche, Menopause, Miscarriage, Preeclampsia.
Respiratory- Risks, function
Cilia, Fluid, Forced expiratory volume, Forced vital capacity, Function, Lung, Mucus, Nitric oxide, Obstruction.
Acute respiratory distress syndrome, Asthma, Bronchopulmonary dysplasia, Bronchiectasis, Central hypoventilation, Chronic obstructive pulmonary disease, Cystic fibrosis (CF), Emphysema, Fibrosis, Hypertension, Invasive Pulmonary Aspergillosis, Pneumonia, Pulmonary Thromboembolism, Tuberculosis.
RNA -Structure/Function, Changes, Risks
Transfer ribonucleic acid (tRNA), Uracil.
Fear, Heat, Pain, Personality, Startle, Surgery, Temperature.
Skin- Traits, Risks/Susceptibilities, Disorders, Sensitivities, Quality
Acne, Advanced glycation end products, Cutis laxa, Elanocytic nevi (moles), Eczema, Melanin, Nevus, Psoriasis, Sun, Vitiligo.
Darier disease, Dermatitis, Dyskeratosis congenita, Ectodermal dysplasia, Epidermolysis bullosa, Fibrofolliculomas, Hypohidrotic X-linked ectodermal dysplasia, Palmoplantaris striata, Porphyria, Skin fragility woolly hair syndrome, Xeroderma pigmentosum.
Sleep- Sleeping patterns, Tendencies, Traits
Circadian Rhythm, Duration, Quality.
Thyroid- Risks/Susceptibilities, Function
Parathyroid, Free T3, Free T4, Thyroid peroxidase, Thyroid-stimulating hormone (TSH), Volume.
Generalized thyroid hormone resistance, Goiter, Hashimoto, Hyperthyroid, Hypothyroid, Thyroid Dyshormonogenesis,
Traits - Body Odor, Personality, Behavior, Features
Eyes, Facial, Hair, Pigment, Strength, Talent, Taste.
Toxins- Detoxification ability, sensitivities, hormones, heavy metals, environmental
Chemicals, Diet, Industrial; Phase I detoxification, Phase II detoxification.
Arsenic, Cyclic Carbonates, Esters, Free Radicals, Monomethylarsonic acid, Polycyclic Aromatic Hydrocarbons, Xenobiotics.
Urate- Levels, Ability to breakdown/Remove, Function, Risks
Beta-aminoisobutyric acid, Blood urea nitrogen (BUN), Uric.
Vaccine- Response, Risks
Anthrax, Hepatitis B, Herpes, Influenza, Meningococcal, Measles, Mumps, and Rubella (MMR), Smallpox.
Vascular- Deficiencies, Risks/Susceptibilities
Endothelium dependent vasodilation, Formation, Vasodilation, Vasculitis, Volume.
Aortic aneurysm, Aortopathy, Atherosclerosis, Deep vein thrombosis (DVT), Ischemic stroke, Kawasaki disease, Peripheral artery disease, Small vessel occlusion, Supravalvar aortic stenosis, Vascular calcification, Venous thromboembolism.
Vitamins- Deficiencies, Metabolism problems (absorption), Build up
Molybdenum, Riboflavin- B2, Pantothenate- B5, Pyridoxine (B6), Biotin- B7, Inositol- B8, Folate- B9, B12, C, Choline, D, E, K.
Virus- Immunity, Risks/Susceptibilities
Cytomegalovirus, COVID, Swine flu (H1N1), Hepatitis B, Human papillomavirus (HPV), Herpes Simplex virus (HSV), Epstein-Barr virus (EB), Malaria, SARS.
Weight- Risks, Abilities, Traits, Eating behavior, Fat loss in response to exercise
Adiponectin, Birth, BMI, Obesity & Weight Loss Markers, Waist size.
We Value Privacy
At Genome It All, we value your privacy! We will not sell or share your data. We also do not ask for any major identifiers, such as Social Security numbers.
If you would like 23andme Interpretation
To order a report on over 175 SNPs
You must already have 23andme raw data that can be emailed.
Please ensure your testing was completed before August 2017 to ensure all SNPs can be reported. 23andme's current Chip v5 lacks many SNPs that is needed.
Turn around time can be around one week, but typically sooner.
OPTION: RAW DATA ONLY!
We also offer an option for ordering genetic testing that provides raw data that includes your results on ~700,000 SNPs only! With this option, you will NOT receive any additional reporting such as: Genotype, health, totals, or summary reports.
You will only receive the raw data file in the form of a text document.
Any sales or specials do not apply to purchases of raw data only!