Health Conditions

43,676 conditions with known genetic associations in our database.

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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)
Infantile
349 variants Other
Triglyceride to Phosphoglyceride Ratio
349 variants Other
Balding Type 1
348 variants Other
Multiple Congenital Exostosis
346 variants Other
Collagen 6-related Myopathy
345 variants Other
Morning Person
345 variants Other
Gut Microbial Network Clusters (pink (at 1 Year) X Any Breastfeeding (3 Months) Interaction
343 variants Other
Household Income (mtag)
343 variants Other
Mowat-wilson Syndrome
343 variants Other
Chronic
342 variants Other
Congenital Myotonia
340 variants Other
Glycine Levels
340 variants Other
Reticulocyte Percentage (ukb Data Field 30240)
339 variants Other
Leukocyte Telomere Length
338 variants Other
Muir-torré Syndrome
337 variants Other
Cognitive Performance
336 variants Other
Epidermolysis Bullosa Dystrophica
336 variants Other
Birth Weight
335 variants Other
Highest Math Class Taken
335 variants Other
Mitochondrial Complex Ii Deficiency
335 variants Other
Autosomal Recessive Form
333 variants Other
Reticulocyte Count (ukb Data Field 30250)
333 variants Other
Chédiak-higashi Syndrome
331 variants Other
Creatinine Levels in Bottom 99% of Individuals By Creatinine Levels
331 variants Other
Metachromatic Leukodystrophy
331 variants Other
Blood Cell Traits Latent Factor 2 (red Cell)
330 variants Other
Multiple
330 variants Other
Saldino-mainzer Syndrome
330 variants Other
Autosomal Dominant Form
328 variants Other
Autosomal Dominant Hypocalcemia 1
328 variants Other
Autosomal Recessive 23
326 variants Other
Phosphatidylinositol(36:2)_[m-h]1- Levels
326 variants Other
Weight (ukb Data Field 21002)
326 variants Other
Asphyxiating Thoracic Dystrophy 3
325 variants Other
Weight (mean, Inv-normal Transformed)
325 variants Other
Weight (maximum, Inv-normal Transformed)
323 variants Other
Chuvash Polycythemia
322 variants Other
Familial Hypocalciuric Hypercalcemia
322 variants Other
Eosinophill Count (ukb Data Field 30150)
320 variants Other
Medium-chain Acyl-coenzyme A Dehydrogenase Deficiency
320 variants Other
Smoking Cessation
320 variants Other
Emery-dreifuss Muscular Dystrophy 5
319 variants Other
Granulomatous Disease
319 variants Other
Interferon-related Traits
319 variants Other
Achondrogenesis
318 variants Other
Neurodevelopmental Delay
318 variants Other
Autosomal Dominant 16
317 variants Other
Concentration of Very Large Hdl Particles
317 variants Other
Glycoprotein Acetyls Levels
317 variants Other
Average Diameter For Hdl Particles
316 variants Other
Developmental and Epileptic Encephalopathy 94
313 variants Other
General Risk Tolerance (mtag)
312 variants Other
Mps-ii
312 variants Other
Lipoprotein (a) Levels
311 variants Other
Post-traumatic Stress Disorder
310 variants Other
Transient Neonatal
310 variants Other
Central Core Myopathy
309 variants Other
Familial Adenomatous Polyposis 4
309 variants Other
Mean Corpuscular Volume (mcv, Mean, Inv-norm Transformed)
309 variants Other
Type V
309 variants Other
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