Health Conditions
43,676 conditions with known genetic associations in our database.
All(43,676)
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)
Reaction Time
Fabry Disease
Hearing Loss
Whole Body Water Mass (ukb Data Field 23102)
Diffuse Plaques (snp X Snp Interaction)
Merosin Deficient Congenital Muscular Dystrophy
Bronchiectasis with or Without Elevated Sweat Chloride 1
Mean Arterial Pressure
Low-density Lipoprotein Levels (mtag)
Bioavailable Testosterone Levels
Forced Vital Capacity (fvc)
Height (maximum, Inv-normal Transformed)
Resistance to Covid-19 Infection (exposed Negative Vs Positive)
Qt Interval
Adiposity (multivariate Analysis)
Childhood Absence
Forced Expiratory Volume in 1 Second (fev1)
Height (minimum, Inv-normal Transformed)
Brugada Syndrome
Basophil Count
Baseline Memory in Impaired Cognition
Connective Tissue Disorder
Progressive Sclerosing Poliodystrophy
Alkaline Phosphatase (ukb Data Field 30610)
Cutis Laxa
Gut Microbial Network Clusters (pink (at 1 Year) X Household Furry Pet Dog (3 Months) Interaction
Walker-warburg Congenital Muscular Dystrophy
7 Conditions
Rett Syndrome
Very Long Chain Acyl-coa Dehydrogenase Deficiency
Distal Hereditary Motor
Neuronopathy
Leber Congenital Amaurosis
Peutz-jeghers Syndrome
Bardet-biedl Syndrome 14
Blood Cell Traits Latent Factor 22 (white Cell)
Maple Syrup Urine Disease
Monocyte Count (ukb Data Field 30130)
Arrhythmogenic Right Ventricular Cardiomyopathy
Serum Creatinine Levels
Hyperaldosteronism
Baller-gerold Syndrome
Immature Fraction of Reticulocytes
Color Vision Defects (deutan-protan)
Leber Congenital Amaurosis 8
Hair Color
Birt-hogg-dube Syndrome
Refractive Error
Cowden Syndrome 1
Kbg Syndrome
Polyunsaturated Fatty Acids to Saturated Fatty Acids Ratio
Leigh Syndrome
Hereditary Sensory and Autonomic
Congenital Contractural Arachnodactyly
Xeroderma Pigmentosum
Autosomal Recessive Limb-girdle Muscular Dystrophy Type 2a
Gut Microbial Network Clusters (salmon (at 1 Year) X Any Breastfeeding (3 Months) Interaction
Seizure
Serum Albumin Levels
Fev1/fvc Ratio
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