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)
Nasopharyngeal Carcinoma (snp X Snp Interaction)
81 variants Cancer
Neuroticism Conditioned On Educational Attainment (multi-trait Conditioning and Joint Analysis)
81 variants Other
Nightmare
81 variants Other
Phosphatidylcholine(38:4)_[m+h]1+/phosphatidylethanolamine(41:4)_[m+h]1+ Levels
81 variants Other
Phosphatidylinositol(34:2)_[m-h]1- Levels
81 variants Other
Primary Ciliary Dyskinesia 14
81 variants Dermatologic
Primary Ciliary Dyskinesia 15
81 variants Dermatologic
Prostate Cancer (snp X Snp Interaction)
81 variants Cancer
Ratio of Omega-6 Fatty Acids to Total Fatty Acids
81 variants Other
Time-dependent Creatinine Clearance Change Response to Tenofovir Treatment in Hiv Infection (time and Treatment Arm Interaction)
81 variants Other
Venous Thromboembolism Adjusted For Sickle Cell Variant Rs77121243-t
81 variants Hematologic
Vnn1 Protein Levels
81 variants Other
Youthful Appearance (self-reported)
81 variants Other
Zttk Syndrome
81 variants Other
3-methylglutaconic Aciduria Type 3
80 variants Other
Acute Intermittent Porphyria
80 variants Other
Anxiety Disorder
80 variants Other
Birth Size (multivariate Analysis)
80 variants Other
Cc2d2a-related Disorder
80 variants Other
Centronuclear
80 variants Other
Cfhr2 Protein Levels
80 variants Other
Cholesteryl Ester Levels in Large Vldl
80 variants Other
Congenital Anomaly of Kidney and Urinary Tract
80 variants Renal
Congenital Muscular Dystrophy Due to Integrin Alpha-7 Deficiency
80 variants Other
Coronary Artery Disease or Factor Vii Levels (pleiotropy)
80 variants Cardiovascular
Digenic
80 variants Other
Distal Arthrogryposis Type 2b1
80 variants Other
Epidermolysis Bullosa Dystrophica Inversa
80 variants Other
Essential Hypertension (phecode 401.1)
80 variants Cardiovascular
Familial Cold Autoinflammatory Syndrome 1
80 variants Other
Fucosidosis
80 variants Other
Haim-munk Syndrome
80 variants Other
Hdl Cholesterol Levels X Long Total Sleep Time Interaction (2df Test)
80 variants Metabolic
Hyper-igm Syndrome Type 1
80 variants Other
Hyperopia
80 variants Other
Intellectual Developmental Disorder with Dysmorphic Facies and Behavioral Abnormalities
80 variants Other
Knobloch Syndrome
80 variants Other
Mean Arterial Pressure X Alcohol Consumption Interaction (2df Test)
80 variants Other
Microcephaly 9
80 variants Other
Peroxisome Biogenesis Disorder 7a (zellweger)
80 variants Other
Perry Syndrome
80 variants Other
Phospholipids to Total Lipids Ratio in Idl
80 variants Metabolic
Pon2 Protein Levels
80 variants Other
Pontocerebellar Hypoplasia Type 1a
80 variants Other
Pursuit Maintenance Gain
80 variants Other
Total Bilirubin Levels X Insomnia Interaction
80 variants Other
Total Lipid Levels in Medium Hdl
80 variants Metabolic
Tpsab1 Protein Levels
80 variants Other
Triglyceride Levels in Large Ldl
80 variants Other
Trunk Fat Mass
80 variants Other
Uveal Melanoma
80 variants Cancer
Waardenburg Syndrome Type 1
80 variants Other
White Blood Cell Count (neutrophil)
80 variants Other
Acne Vulgaris
79 variants Other
Adgrb3 Protein Levels
79 variants Other
Bmi (adjusted For Smoking Behaviour)
79 variants Metabolic
Body Mass Index (joint Analysis Main Effects and Smoking Interaction)
79 variants Other
Bone Stiffness Index
79 variants Other
Brody Myopathy
79 variants Other
Cerebroretinal Microangiopathy with Calcifications and Cysts 1
79 variants Ophthalmic
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