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)
Distal Spinal Muscular Atrophy
Dmd-related Disorder
Ectodermal Dysplasia 10a
Feeling Fed-up
Frailty (factor 5 - Poorer Cognition)
Geleophysic Dysplasia
Gut Microbial Network Clusters (blueviolet (at 3 Months) X Vaginal Birth Interaction
Gut Microbiota (beta Diversity)
Hdgf Protein Levels
Hereditary Spastic Paraplegia 2
Itgb7 Protein Levels
Lefty2 Protein Levels
Macrothrombocytopenia
Myo15a-related Disorder
Nuclear Type 2
Number of Puzzles Correctly Solved (baseline)
Phosphatidylcholine(36:3)_[m+oac]1-/phosphatidylserine(40:2)_[m-h]1- Levels
Phosphatidylinositol(40:6)_[m-h]1- Levels
Pm20d1 Protein Levels
Polyunsaturated Fatty Acids
Principal Component-derived Dietary Pattern 1
Rod-cone Dystrophy
Sparcl1 Protein Levels
Sphingomyelin(38:1)_[m+h]1+ Levels
Testosterone Levels in Postmenopausal Women
Trichothiodystrophy 1
Type C2
Znf469-related Disorder
Zp3 Protein Levels
Abo Protein Levels
Arthrogryposis Multiplex Congenita
Asah2 Protein Levels
Bartter Syndrome
Basophil (absolute Count, Maximum, Inv-norm Transformed)
Behcet's Disease
Breast Size
Childhood Onset Glut1 Deficiency Syndrome 2
Cholesteryl Esters in Vldl
Cigarette Consumption X Hours Spent Using Computers Interaction
Congenital Microcephaly - Severe Encephalopathy - Progressive Cerebral Atrophy Syndrome
Congenital Prothrombin Deficiency
Corneal Curvature
Cornelia De Lange Syndrome 5
Corpus Callosum Volume (mostest)
Ctrc Protein Levels
Diacylglycerol(34:1)_[m+h-h2o]1+ Levels
Dxa-bone Mineral Density (head) (ukb Data Field 23226)
Faslg Protein Levels
Fatal Mitochondrial Disease Due to Combined Oxidative Phosphorylation Defect Type 3
Fvc X Serum 25-hydroxyvitamin D Interaction in Ever Smokers (2df Test)
Gc Protein Levels
Hereditary Spastic Paraplegia 8
Hypohidrotic/hair/nail Type
Il1rap Protein Levels
Leber Congenital Amaurosis 9
Mean Volume of Bilateral Amygdala
Methylcrotonyl-coa Carboxylase Deficiency
Mitochondrial Complex V (atp Synthase) Deficiency
Mln Protein Levels
Motor Premotor Area
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