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Genetic Predisposition Test

The most comprehensive genetic test on the market! We test for a total of 124 genetic traits!

31 Disease Conditions
53 Carrier Status Conditions
12 Drug Response genes
6 Wellness Tests
11 Traits
11 Addictions



Genetic Predisposition Order Now - $99

Genetic Predisposition and Ancestry* Order Now - $125

*To learn more about our Ancestral test, please click here

You will receive an extensive, understandable, report reviewing you results. The report shows the multiple single nucleotide polymorphisms (SNP) markers that were tested, the findings, and your logarithmic, statistical, relative, level of risk, as well as internal stress level potential problems. The information in the report is based on the latest scientific research.

Here are all the genetic diseases, carrier status, drug response, wellness, traits and addictions that we can identify:

Exfoliation Glaucoma
Chronic Kidney Disease
Multiple Sclerosis
Ulcerative Colitis
Esophageal Squamous Cell Carcinoma (ESCC)
Stomach Cancer (Gastric Cardia Adenocarcinoma)
Atrial Fibrillation
Bipolar Disorder
Breast Cancer
Celiac Disease
Colorectal Cancer
Coronary Heart Disease
Lung Cancer
Parkinson's Disease
Prostate Cancer
Scleroderma (Limited Cutaneous Type)
Type 2 Diabetes
Venous Thromboembolism
Age-related Macular Degeneration
Alzheimer's Disease
Crohn's Disease
Lupus (Systemic Lupus Erythematosus)
Primary Biliary Cirrhosis
Restless Legs Syndrome
Rheumatoid Arthritis
Type 1 Diabetes

Carrier Status
Hemochromatosis (HFE-related)
Agenesis of the Corpus Callosum with Peripheral Neuropathy (ACCPN)
Alpha-1 Antitrypsin Deficiency
Autosomal Recessive Polycystic Kidney Disease
BRCA Cancer Mutations (Selected)
Beta Thalassemia
Bloom's Syndrome
Canavan Disease
Congenital Disorder of Glycosylation Type 1a (PMM2-CDG)
Connexin 26-Related Sensorineural Hearing Loss
Cystic Fibrosis
D-Bifunctional Protein Deficiency
DPD Deficiency
Dihydrolipoamide Dehydrogenase Deficiency
Factor XI Deficiency
Familial Dysautonomia
Familial Hypercholesterolemia Type B
Familial Hyperinsulinism (ABCC8-related)
Familial Mediterranean Fever
Fanconi Anemia (FANCC-related)
G6PD Deficiency
GRACILE Syndrome
Gaucher Disease
Glycogen Storage Disease Type 1a
Glycogen Storage Disease Type 1b
Hereditary Fructose Intolerance
Hypertrophic Cardiomyopathy (MYBPC3 25bp-deletion)
LAMB3-related Junctional Epidermolysis Bullosa
Leigh Syndrome, French Canadian Type (LSFC)
Limb-girdle Muscular Dystrophy
Maple Syrup Urine Disease Type 1B
Medium-Chain Acyl-CoA Dehydrogenase (MCAD)
Mucolipidosis IV
Neuronal Ceroid Lipofuscinosis (CLN5- related)
Neuronal Ceroid Lipofuscinosis (PPT1-related)
Niemann-Pick Disease Type A
Nijmegen Breakage Syndrome
Pendred Syndrome
Primary Hyperoxaluria Type 2 (PH2)
Rhizomelic Chondrodysplasia Punctata Type 1 (RCDP1)
Salla Disease
Sickle Cell Anemia & Malaria Resistance
Sjögren-Larsson Syndrome
TTR-Related Cardiac Amyloidosis
TTR-Related Familial Amyloid Polyneuropathy
Tay-Sachs Disease
Torsion Dystonia
Tyrosinemia Type I
Usher Syndrome Type I (PCDH15-related)
Usher Syndrome Type III
Zellweger Syndrome Spectrum

Wellness Tests
Alcohol Flush
Caffeine Metabolism
Deep Sleep
Lactose Intolerance
Muscle Performance
Sleep Movement

Asparagus Odor Detection
Back Hair (available for men only)
Bald Spot (available for men only)
Digit Ratio
Earlobe Type
Earwax Type
Facial Features
Male Hair Loss (available for men only)
Newborn Hair Amount
Photic Sneeze Reflex
Taste Preference and Perception

Alcoholism (alcohol cravings)
Alcoholism (alcohol dependence)
Alcoholism (withdrawal seizures)
Cannabis dependence
Cocaine dependence
Cocaine-induced paranoia
Gambling addiction
Heroin addiction
Nicotine dependence (tobacco addiction)

Samples for DNA extraction are taken using buccal swabs (i.e. cheek swabs) and returning it to Viaguard. Complete instructions are enclosed in the kit.

Results in 7-10 days.

If you are a medical professional, please contact us on our partnering program.