Health Conditions
52,757 conditions with known genetic associations in our database.
All(52,757)
Other(43,676)
Cardiovascular(1,793)
Metabolic(1,614)
Renal(1,319)
Cancer(1,257)
Neurological(750)
Ophthalmic(535)
Gastrointestinal(367)
Hematologic(345)
Respiratory(323)
Autoimmune(265)
Dermatologic(221)
Pharmacogenomic(163)
Musculoskeletal(129)
Dna Methylation-estimated Plasminogen Activator Inhibitor-1 Levels
Dominant Beta-thalassemia
Dpp7 Protein Levels
Dysphagia
Ease of Skin Tanning
Endou Protein Levels
Enpp6 Protein Levels
Esophageal Adenocarcinoma
F-fish Liking (derived Food-liking Factor)
F-seafood Liking (derived Food-liking Factor)
Facial Morphology (factor 21, Depth of Nasal Alae)
Familial Juvenile Hyperuricemic Nephropathy Type 2
Fanconi Renotubular Syndrome 4 with Maturity-onset Diabetes of the Young
Fev1 or Gastro-oesophageal Reflux Disease (pleiotropy)
Fev1/fvc or Inflammatory Bowel Disease (pleiotropy)
Generalized Hypotonia
Gestational Age At Birth (child Effect)
Glycerate Levels
Glycine Levels (ukb Data Field 23462)
Gut Microbiome Abundance (class Clostridium Sensu Stricto Sp. 17 (at 1 Year) X Household Furry Pet Dog (3 Months) Interaction
Hair/tooth Type with or Without Hypohidrosis
Height At Take-off
Hepatic Steatosis
Hexanoylcarnitine Levels
Hypercholanemia
Hyperinsulinism-hyperammonemia Syndrome
Hypertrophic Cardiomyopathy (sarcomere-negative)
Hypertrophic Cardiomyopathy 13
Igf1r Protein Levels
Immunodeficiency 18
Inherited Phaeochromocytoma and Paraganglioma Excluding Nf1
Insulin Resistance
Itga5 Protein Levels
Itgb1bp2/mitd1 Protein Level Ratio
Joubert Syndrome 13
Lama4 Protein Levels
Ldlr Protein Levels
Left Ventricular Global Radial Strain
Leopard Syndrome 2
Leukocyte Adhesion Deficiency Type Ii
Leukocyte Immunoglobulin-like Receptor Subfamily B Member 1 Levels
Lhpp Protein Levels
Lipid Traits (pleiotropy) (hipo Component 1)
Low Hdl-cholesterol Levels
Low-carbohydrate Diet (lcd) Score
Lpl Protein Levels
Ly96 Protein Levels
Lymphocytic Leukemia
Lymphoid Neoplasms (somatic Mutation Group 2 Phenocluster)
Lysophosphatidylcholine-o_16:1_[m+h]1+/lysophosphatidylcholine-p_16:0_[m+h]1+ Levels
Mep1a Protein Levels
Microcytic Anemia
Missouri Type
Mkb Type
Moderate-to-late Spontaneous Preterm Birth
Multiple Myeloma or Monoclonal Gammopathy of Undetermined Significance
Myasthenia Gravis
Myo5b-related Disorder
Myocardial Infarction (phecode 411.2)
Neurodevelopmental Disorder with or Without Autism or Seizures
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