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)
Hair Colour (natural, Before Greying): Red (ukb Data Field 1747_2)
89 variants Other
Hearing Difficulty
89 variants Other
Immature Platelet Count
89 variants Hematologic
Joubert Syndrome with Renal Defect
89 variants Renal
Juvenile Retinoschisis
89 variants Other
Kidney Sinus Volume
89 variants Renal
Kleefstra Syndrome 2
89 variants Other
Mitochondrial Dna Copy Number (adjusted)
89 variants Other
Neonatal Form
89 variants Other
Phospholipid Levels in Hdl
89 variants Metabolic
Phospholipid Levels in Small Vldl
89 variants Metabolic
Sick Sinus Syndrome 1
89 variants Other
Subcortical Volume (min-p)
89 variants Other
Sulfite Oxidase Deficiency
89 variants Other
Symmetrical Dyschromatosis of Extremities
89 variants Other
Syndromic X-linked Intellectual Disability Najm Type
89 variants Other
Total Lipid Levels in Large Vldl
89 variants Metabolic
Total Lipid Levels in Small Vldl
89 variants Metabolic
6-month Creatinine Clearance Change Response to Tenofovir Treatment in Hiv Infection (treatment Arm Interaction)
88 variants Other
Anophthalmia-microphthalmia Syndrome
88 variants Other
Ascending Aorta Maximum Area
88 variants Other
Autosomal Recessive Ataxia Due to Ubiquinone Deficiency
88 variants Other
Coronary Artery Disease or Von Willebrand Factor Levels (pleiotropy)
88 variants Cardiovascular
Fbn1-related Disorder
88 variants Other
Femoral Neck Bone Mineral Density
88 variants Other
Hematocrit (minimum, Inv-norm Transformed)
88 variants Other
Inflammatory Bowel Disease (tractor Method with European Ancestry)
88 variants Gastrointestinal
Inflammatory Skin Disease
88 variants Dermatologic
Keratinocyte Cancer (mtag)
88 variants Cancer
Nonalcoholic Fatty Liver Disease (imputed)
88 variants Gastrointestinal
Papillon-lefèvre Syndrome
88 variants Other
Phosphatidylcholine(38:3)_[m+h]1+/phosphatidylethanolamine(41:3)_[m+h]1+/phosphatidate(43:4)_[m+nh4]1+ Levels
88 variants Other
Phospholipid Levels in Medium Hdl
88 variants Metabolic
Piezo1-related Disorder
88 variants Other
Progressive Familial Intrahepatic Cholestasis Type 3
88 variants Gastrointestinal
Response to Amphetamines
88 variants Other
Retinal Arteriolar Tortuosity
88 variants Ophthalmic
Somatic
88 variants Other
Trail Levels
88 variants Other
Triglyceride Levels in Small Hdl
88 variants Other
1,5-anhydroglucitol (1,5-ag) Levels
87 variants Other
3m Syndrome 2
87 variants Other
Alg9 Congenital Disorder of Glycosylation
87 variants Other
Aneurysm-osteoarthritis Syndrome
87 variants Musculoskeletal
Bilirubin Levels
87 variants Other
Cholesterol to Total Lipids Ratio in Very Large Vldl
87 variants Metabolic
Coffin-lowry Syndrome
87 variants Other
Complement Component 3 Deficiency
87 variants Other
Congenital Microvillous Atrophy
87 variants Other
Cpvl Protein Levels
87 variants Other
Developmental and Epileptic Encephalopathy 6b
87 variants Other
Elevated Prostate Specific Antigen [psa] (phecode 796)
87 variants Other
Family History of Alzheimer's Disease
87 variants Neurological
Free Cholesterol to Total Lipids Ratio in Very Small Vldl
87 variants Metabolic
Gracile Syndrome
87 variants Other
Hereditary Mixed
87 variants Other
Hypercalcemia
87 variants Other
Inflammatory Bowel Disease 1
87 variants Gastrointestinal
Leber Congenital Amaurosis 4
87 variants Other
Major Depressive Disorder (mtag)
87 variants Other
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