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)
Threonine Levels
Thrombocythemia 1
Thrombocytopenia 5
Thrombomodulin-related Bleeding Disorder
Tmprss15 Protein Levels
Tmprss3-related Disorder
Tnfsf14 Protein Levels
Toenail Selenium Levels
Total Bilirubin Levels (analysis Model with European Background)
Tp63-related Disorder
Triacylglycerol_52:6_[m+nh4]1+ Levels
Triacylglycerol_56:4_[m+nh4]1+ Levels
Triacylglycerol(50:2)_[m+nh4]1+ Levels
Trpm1-related Disorder
Urinary 3-aminoisobutyrate to Urinary Creatinine Ratio
Vaginal Microbiome Beta Diversity (unweighted Unifrac)
Vaginal Microbiome Metacyc Pathway (pwy-7315|dtdp-n-acetylthomosamine Biosynthesis)
Vaginal Microbiome Relative Abundance (s_finegoldia Magna)
Variant Ab
Vegetarianism
Venous Thromboembolism or Plasminogen Activator Inhibitor 1 Levels (pleiotropy)
Vesicoureteral Reflux 2
Visuospatial Ability
Von Willebrand Disease Type 2b
Waist Circumference Variance
Wechsler Memory Scale Iii Visual Reproduction (visrep) Test 1 Immediate (visrep Imd)
With Hypomyelinating Leukodystrophy
With Variable Ataxia and Seizures
X-21353 Levels
X-linked 104
X-linked 21
X-linked Complicated Corpus Callosum Dysgenesis
1-arachidonoyl-gpe (20:4n6) Levels
1-palmitoyl-2-arachidonoyl-gpe (16:0/20:4) Levels
1-stearoyl-2-oleoyl-gpe (18:0/18:1) Levels
3-hydroxydecanoylcarnitine Levels
3-hydroxyoctanoylcarnitine (1) Levels
5-acetylamino-6-formylamino-3-methyluracil Levels
5alpha-androstan-3alpha,17beta-diol Disulfate Levels
Achalasia
Acromesomelic Dysplasia 2b
Actn2-related Disorder
Adamts2-related Disorder
Ahi1-related Disorder
Alacrima
Albumin Levels (ukb Data Field 23479)
Albuminuria
Alcohol Use Disorder (total Score)
Aldob-related Disorder
Alg8-related Disorder
Alkenylphosphatidylethanolamine (p-18:1/20:3) (a) Levels
Amyotrophic Lateral Sclerosis Type 15
And Digital Anomalies with Developmental Delay
And Dysosteosclerosis
And Endocrine Dysfunction
And Intellectual Disability Syndrome
And Short Stature
And Spasticity
Ano5-related Disorder
App/hbegf Protein Level Ratio
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