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)
Chronotype
466 variants Other
Smoking Initiation (ever Regular Vs Never Regular)
465 variants Other
Spinocerebellar Ataxia
465 variants Other
Usher Syndrome
460 variants Other
Venous Thromboembolism
460 variants Other
Multi-trait Sum Score
459 variants Other
Body Surface Area
456 variants Other
Classic or Attenuated Familial Adenomatous Polyposis
456 variants Other
Congenital Long Qt Syndrome
455 variants Other
Alagille Syndrome Due to A Jag1 Point Mutation
453 variants Other
Sotos Syndrome
453 variants Other
Hereditary Factor Viii Deficiency Disease
452 variants Other
Red Blood Cell Erythrocyte Count (ukb Data Field 30010)
451 variants Other
Werner Syndrome
450 variants Other
Autosomal Recessive Nonsyndromic Hearing Loss 3
448 variants Other
Hereditary
448 variants Other
Hypotonia
447 variants Other
Covid-19 (hospitalized Covid Vs Population)
443 variants Other
Fasting Blood Glucose
443 variants Other
Hematuria
440 variants Other
Monocyte Percentage (ukb Data Field 30190)
440 variants Other
Adrenoleukodystrophy
439 variants Other
Hospitalization Rate in Serious Mental Illnesses
439 variants Other
Mean Reticulocyte Volume (ukb Data Field 30260)
439 variants Other
Congenital
435 variants Other
Hereditary Hemorrhagic Telangiectasia
435 variants Other
Hereditary Spastic Paraplegia 30
435 variants Other
Hereditary Sensory
432 variants Other
Mean Sphered Cell Volume (ukb Data Field 30270)
432 variants Other
Charcot-marie-tooth Disease Axonal Type 2o
431 variants Other
Hand Grip Strength (baseline)
430 variants Other
Autosomal Dominant 9
429 variants Other
Telomere-related
429 variants Other
Attention Deficit Hyperactivity Disorder
427 variants Other
Childhood Body Mass Index
426 variants Other
Type 2a
423 variants Other
Multiple Acyl-coa Dehydrogenase Deficiency
421 variants Other
Peak Expiratory Flow
420 variants Other
Miyoshi Muscular Dystrophy 1
419 variants Other
Catecholaminergic Polymorphic Ventricular Tachycardia
417 variants Other
Red Blood Cell Erythrocyte Distribution Width (ukb Data Field 30070)
417 variants Other
Retinitis Pigmentosa 12
415 variants Other
Global Developmental Delay
414 variants Other
Primary Hyperoxaluria
414 variants Other
Dna Methylation Variation (age Effect)
413 variants Other
Eosinophill Percentage (ukb Data Field 30210)
413 variants Other
Hereditary Spastic Paraplegia 4
413 variants Other
Breast Dense Area
411 variants Other
Usher Syndrome Type 1d
408 variants Other
Autosomal Dominant Alport Syndrome
407 variants Other
Autosomal Recessive Nonsyndromic Hearing Loss 2
407 variants Other
Fev1
407 variants Other
Igf 1 (ukb Data Field 30770)
406 variants Other
Type 2c
406 variants Other
Von Hippel-lindau Syndrome
403 variants Other
Low-density Lipoprotein Levels
402 variants Other
Autosomal Dominant 5
397 variants Other
Glycated Haemoglobin Hba1c Levels (ukb Data Field 30750)
396 variants Other
Igg Glycosylation
395 variants Other
Lymphangiomyomatosis
394 variants Other
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