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)
Body Fat Percentage
372 variants Other
Hepatocellular Carcinoma
372 variants Cancer
Osteoarthritis
370 variants Musculoskeletal
Corneal Resistance Factor (mtag)
369 variants Other
Glanzmann Thrombasthenia
369 variants Other
Parkinson's Disease
369 variants Neurological
Pseudo-hurler Polydystrophy
369 variants Other
Gamma Glutamyl Transpeptidase
368 variants Other
Hypertrophic Cardiomyopathy 4
368 variants Other
Telomere Length (principal Component 1)
368 variants Other
Type 7
368 variants Other
Cardiovascular Disease
367 variants Other
Blood Cell Traits Latent Factor 5 (platelet)
366 variants Hematologic
Familial Temporal Lobe Epilepsy 7
366 variants Neurological
Waist Circumference
366 variants Other
Bethlem Myopathy 2
365 variants Other
Diabetes Mellitus
364 variants Metabolic
Fluid Intelligence Score (baseline)
364 variants Other
Multiple Types
364 variants Other
Autosomal Dominant 2
363 variants Other
Deficiency of Alpha-mannosidase
363 variants Other
Free Testosterone Levels
363 variants Other
Mps-iv-a
363 variants Other
Concentration of Large Hdl Particles
362 variants Other
Haematocrit Percentage (ukb Data Field 30030)
361 variants Other
Ullrich Congenital Muscular Dystrophy 2
361 variants Other
Cigarettes Smoked Per Day
360 variants Other
Pr Interval
360 variants Other
Wolfram Syndrome 1
360 variants Other
Aplastic Anemia
359 variants Hematologic
Menkes Kinky-hair Syndrome
358 variants Other
Congenital Bilateral Aplasia of Vas Deferens From Cftr Mutation
357 variants Other
Galactosylceramide Beta-galactosidase Deficiency
357 variants Other
Autosomal Recessive 5
356 variants Other
Congenital Multicore Myopathy with External Ophthalmoplegia
356 variants Other
Restless Legs Syndrome
356 variants Other
Usher Syndrome Type 2c
353 variants Other
Depressive Symptoms
352 variants Other
Familial Spinal
352 variants Other
Hypertrophic Cardiomyopathy 1
350 variants Other
Rubinstein-taybi Syndrome Due to Crebbp Mutations
350 variants Other
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
Platelet Count (minimum, Inv-norm Transformed)
343 variants Hematologic
Chronic
342 variants Other
Pheochromocytoma/paraganglioma Syndrome 5
342 variants Cancer
Heart Failure
341 variants Cardiovascular
Congenital Myotonia
340 variants Other
Glycine Levels
340 variants Other
Lung Function (fev1)
340 variants Respiratory
Chronic Obstructive Pulmonary Disease Liability (machine Learning-based Score)
339 variants Respiratory
Platelet Count (maximum, Inv-norm Transformed)
339 variants Hematologic
Reticulocyte Percentage (ukb Data Field 30240)
339 variants Other
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