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)
Gask1a Protein Levels
48 variants Other
Glucocorticoid Deficiency with Achalasia
48 variants Other
Headache
48 variants Other
Hepatocyte Growth Factor Levels
48 variants Other
Hepatocyte Growth Factor-like Protein Levels
48 variants Other
Hypertrophic Cardiomyopathy 10
48 variants Other
Hypertrophic Cardiomyopathy 11
48 variants Other
Inhbc Protein Levels
48 variants Other
Joubert Syndrome 14
48 variants Other
Joubert Syndrome 18
48 variants Other
Ldl (weighted Gwa)
48 variants Other
Leg1 Protein Levels
48 variants Other
Lilra3 Protein Levels
48 variants Other
Low Fluorescent Percentage of Reticulocytes
48 variants Other
Lztr1-related Disorder
48 variants Other
Magnesium (mg, Mean, Inv-norm Transformed)
48 variants Other
Mme Protein Levels
48 variants Other
Msln Protein Levels
48 variants Other
Ncam2 Protein Levels
48 variants Other
Nicotine Dependence
48 variants Other
Nystagmus
48 variants Other
Percent Mammographic Density
48 variants Other
Polycystic Ovary Syndrome
48 variants Other
Pontocerebellar Hypoplasia Type 1b
48 variants Other
Ryr1-related Myopathy
48 variants Other
Sjögren's Syndrome
48 variants Other
Spinocerebellar Ataxia Type 19/22
48 variants Other
Spinocerebellar Ataxia Type 5
48 variants Other
Torsion Dystonia 6
48 variants Other
Trichohepatoenteric Syndrome 1
48 variants Other
Triglycerides in Small Hdl (ukb Data Field 23578)
48 variants Other
Triglycerides in Very Small Vldl (ukb Data Field 23522)
48 variants Other
Type 8
48 variants Other
Vaginal Microbiome Metacyc Pathway (catechol-ortho-cleavage-pwy|catechol Degradation to β-ketoadipate)
48 variants Other
Warburg Micro Syndrome 2
48 variants Other
With Progressive Scoliosis 1
48 variants Other
Yeast Infection
48 variants Other
A Subunit
47 variants Other
And Brain Abnormalities
47 variants Other
Arid1b-related Bafopathy
47 variants Other
Ascending Aorta Maximum Area (mtag)
47 variants Other
Autosomal Recessive Spinocerebellar Ataxia 7
47 variants Other
Cardiofaciocutaneous Syndrome 1
47 variants Other
Carotid Intima Media Thickness
47 variants Other
Cd1c Protein Levels
47 variants Other
Ceramide(41:2)_[m-h]1- Levels
47 variants Other
Cfh-related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type Ii
47 variants Other
Cntn1 Protein Levels
47 variants Other
Coach Syndrome 1
47 variants Other
Concentration of Very Large Vldl Particles (ukb Data Field 23488)
47 variants Other
Congenital Myasthenic Syndrome 13
47 variants Other
Cpa1 Protein Levels
47 variants Other
Ctack Levels
47 variants Other
Cyp27a1-related Disorder
47 variants Other
Dilated Cardiomyopathy 1m
47 variants Other
Facial Dysmorphism
47 variants Other
Factor I Deficiency
47 variants Other
Finnish Type Amyloidosis
47 variants Other
Gaucher Disease Due to Saposin C Deficiency
47 variants Other
Gestational Thrombocytopenia
47 variants Other
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