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Genetic Predisposition Test

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

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

DEDICATED TO A LONGER AND HEALTHIER LIFE

Genome

Genetic Predisposition Order Now - $89

Genetic Predisposition and Ancestry* Order Now - $149

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

You will receive a clear and comprehensive describing the multiple single nucleotide polymorphism (SNP) markers that were tested, statistical level of risk, and potential stress level issues. All information is based on the latest scientific research.

Below is a list of genetic diseases, carrier status, drug response, wellness, traits and addictions we can identify:


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

Carrier Status
Hemochromatosis (HFE-related)
ARSACS
Agenesis of the Corpus Callosum with Peripheral Neuropathy (ACCPN)
Alpha-1 Antitrypsin Deficiency
Autosomal Recessive Polycystic Kidney
BRCA Cancer Mutations (Selected)
Beta Thalassemia
Bloom's Syndrome
Canavan
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
Glycogen Storage Type 1a
Glycogen Storage 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 Type 1B
Medium-Chain Acyl-CoA Dehydrogenase (MCAD)
Mucolipidosis IV
Neuronal Ceroid Lipofuscinosis (CLN5- related)
Neuronal Ceroid Lipofuscinosis (PPT1-related)
Niemann-Pick Type A
Nijmegen Breakage Syndrome
Pendred Syndrome
Phenylketonuria
Primary Hyperoxaluria Type 2 (PH2)
Rhizomelic Chondrodysplasia Punctata Type 1 (RCDP1)
Salla
Sickle Cell Anemia & Malaria Resistance
Sjögren-Larsson Syndrome
TTR-Related Cardiac Amyloidosis
TTR-Related Familial Amyloid Polyneuropathy
Tay-Sachs
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

Traits
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

Addiction
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) then returned to Viaguard. Complete instructions are enclosed in the kit.

Results in 7-10 days.

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

* This test is not available for sale in certain countries- Please click here for the list