Full List of Conditions

Drug Response (Medication)

Identify how your genes may affect your response to medications such as cancer treatments, cholesterol lowering drugs and more. See the complete list below:

  • Abacavir Hypersensitivity
  • Aminoglycoside Induced Antibiotics Hearing Loss
  • Caffeine Metabolism
  • Carbamazepine Hypersensitivity
  • Clopidrogel Metabolism
  • Methotrexate Toxicity
  • Estrogen supplementation (HRT, birth control): risk of venous thrombosis (females only)
  • Statin Induced Myopathy
  • Statin protection against myocardial infarction
  • Tamoxifen Response
  • Warfarin Metabolism

Pre-Pregnancy Planning

Reveal disease traits potentially passed to your children like cystic fibrosis, Gaucher disease, Tay-Sachs and hearing loss. See the complete list below:

  • 3-Methylcrotonyl-CoA carboxylase deficiency
  • Acrodermatitis enteropathica
  • Alpha-1 antitrypsin deficiency
  • Amyotrophic lateral sclerosis
  • Argininosuccinate lyase deficiency
  • Autoimmune polyglandular syndrome, type I
  • Bartter syndrome type 4A
  • Beta-ketothiolase deficiency
  • Beta-thalassemia
  • Biotinidase deficiency
  • Bloom syndrome
  • Canavan disease
  • Carnitine deficiency, primary systemic
  • Cerebrotendinous xanthomatosis
  • Citrullinemia type I
  • Corticosterone methyl oxidase deficiency
  • Crigler-Najjar syndrome
  • Cystic fibrosis
  • Diabetes, permanent neonatal
  • Dihydropyrimidine dehydrogenase deficiency
  • Dubin-Johnson syndrome
  • Ehlers-Danlos syndrome, dermatosparaxis
  • Ehlers-Danlos syndrome, hypermobility
  • Ehlers-Danlos syndrome, kyphoscoliotic
  • Ethylmalonic aciduria
  • Factor XI deficiency
  • Familial dysautonomia
  • Familial Mediterranean fever
  • Fanconi anemia
  • Galactokinase deficiency
  • Galactosemia
  • Gaucher disease
  • Glutaric acidemia, type 1
  • Glycogen storage disease, type 1A
  • GM1-gangliosidosis
  • Hearing loss, DFNB1 and DFNB9 nonsyndromic
  • Hearing loss, DFNB59 nonsyndromic
  • Hemochromatosis
  • Hemoglobin C
  • Hemoglobin E
  • HMG-CoA lyase deficiency
  • Homocystinuria, cblE type
  • Homocystinuria, classic
  • Hurler syndrome
  • Krabbe disease
  • Lipoprotein lipase deficiency, familial
  • Maple syrup urine disease
  • Medium-chain acyl-CoA dehydrogenase deficiency
  • Methylmalonic acidemia
  • MTHFR deficiency
  • Mucolipidosis II
  • Mucolipidosis III
  • Mucolipidosis IV
  • Multiple carboxylase deficiency
  • Nephrotic syndrome, steroid-resistant
  • Niemann-Pick disease
  • Phenylketonuria
  • Polycystic kidney disease
  • Pompe disease
  • Prekallikrein deficiency
  • Propionic acidemia
  • Prothrombin deficiency
  • Rh-null syndrome
  • Rickets, pseudovitamin D-deficiency
  • Sandhoff disease
  • Short-chain acyl-CoA dehydrogenase deficiency
  • Sick sinus syndrome
  • Sickle cell disease
  • Spherocytosis, hereditary
  • Tay-Sachs disease
  • Tay-Sachs pseudodeficiency
  • Thrombocytopenia, congenital amegakaryocytic
  • Tyrosinemia
  • Very long-chain acyl-CoA dehydrogenase deficiency
  • Von Willebrand disease type 2 Normandy
  • Von Willebrand disease type 3

Health Conditions

Learn if you might have an increased propensity for obesity, cancers, diabetes, heart disease and more. See the complete list below:

Condition African Asian Caucasian Hispanic
Age-related macular degeneration X X
Alzheimer’s disease, late onset X X X X
Amyotrophic lateral sclerosis (sporadic) X
Asthma X X
Atrial fibrillation X X
Breast cancer (females only) X X X X
Colorectal cancer X X
Coronary artery disease X X
Diabetes, Type 1 X X
Diabetes, Type 2 X X X
Exfoliation Glaucoma X
Hypertension X X
Leukemia, chronic lymphocytic X
Lung cancer X X
Melanoma X
Multiple sclerosis X
Myocardial infarction X X
Obesity X X
Osteoarthritis X X
Parkinson’s disease X
Peripheral arterial disease X
Prostate cancer (males only) X X X X
Psoriasis X
Rheumatoid arthritis X X
Systemic lupus erythematosus X X X X
Ulcerative colitis X X
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