Conditions
351 conditions with linked SNPs, from common traits to rare inherited disorders.
#
A
- Abdominal aortic aneurysm9
- ABO blood group5
- Achondroplasia13
- Acute intermittent porphyria2
- Acute lymphoblastic leukemia7
- Addiction2
- Addison's disease2
- Age related macular degeneration21
- Age-related hearing impairment1
- Agenesis of the corpus callosum with peripheral neuropathy2
- AIDS6
- Alcoholism10
- Allergies4
- Allograft rejection4
- Alopecia areata1
- Alpha thalassemia68
- Alpha-1 antitrypsin deficiency2
- Alport syndrome2
- Alzheimer's disease177
- Amyloidosis3
- Amyotrophic lateral sclerosis5
- Aneurysm6
- Angioedema18
- Ankylosing spondylitis20
- Anorexia nervosa1
- Antithrombin III deficiency1
- Argininosuccinate lyase deficiency30
- Arthritis4
- Asian flush1
- Asthma37
- Ataxia4
- Atherosclerosis4
- Atopic dermatitis7
- Atrial fibrillation12
- Attention deficit hyperactivity disorder6
- Autism29
- Autoimmune disease2
- Autoimmune thyroiditis2
- Autosomal recessive polycystic kidney disease7
B
- Baldness12
- BAP1 tumor predisposition syndrome2
- Barth syndrome6
- Bartter syndrome1
- Basal cell carcinoma5
- Behçet's disease1
- Benign familial neonatal-infantile seizures4
- Beta thalassemia4
- Bicuspid aortic valve1
- Bipolar disorder45
- Birt-hogg-dube syndrome2
- Bladder cancer13
- Blindness1
- Blood1
- Blood pressure19
- Bloom syndrome1
- Bowen-conradi syndrome1
- Breast cancer1,727
- Brown-vialetto-van laere syndrome51
- Brugada syndrome3
C
- Canavan disease34
- Cancer30
- Cataracts2
- Celiac disease8
- Central core disease3
- Cerebral amyloid angiopathy5
- Cerebral cavernous malformation2
- Cervical cancer2
- Charcot-marie-tooth3
- Charcot-marie-tooth disease2
- Cholesterol16
- Chorionic plate inflammation2
- Choroideremia6
- Chronic kidney disease5
- Chronic obstructive pulmonary disease13
- Cleft palate3
- Cluster headaches1
- Coenzyme Q10 deficiency20
- Colon cancer12
- Colorblind2
- Colorectal cancer61
- Conduct disorder2
- Congenital adrenal hyperplasia29
- Congenital disorder of glycosylation2
- Congenital erythropoietic porphyria1
- Congenital myasthenic syndrome1
- Coronary artery disease158
- Crigler-najjar syndrome1
- Crohn's disease65
- Cystic fibrosis532
D
E
F
- Fabry disease2
- Familial dysautonomia3
- Familial hypercholesterolemia138
- Familial hyperlipoproteinemia3
- Familial hypertrophic cardiomyopathy141
- Familial mediterranean fever28
- Fanconi anemia9
- Fatal familial insomnia2
- Fetal alcohol syndrome1
- Fibrodysplasia ossificans progressiva7
- Fibromyalgia5
- Focal segmental glomerulosclerosis22
- Friedreich's ataxia36
- Frontotemporal dementia12
- Fuchs' dystrophy4
G
H
- Hashimoto's thyroiditis1
- HDL cholesterol11
- Hearing loss14
- Heart disease54
- Height13
- Hemochromatosis6
- Hemophagocytic lymphohistiocytosis25
- Hemophilia56
- Hepatitis c3
- Hereditary diffuse gastric cancer22
- Hereditary factor IX deficiency disease1
- Hereditary fructosuria3
- Hereditary hemorrhagic telangiectasia25
- Hereditary leiomyomatosis and renal cell cancer6
- Hereditary pancreatitis12
- Herpes4
- High blood pressure13
- Hirschsprung disease3
- HIV14
- Hodgkin lymphoma1
- Homocystinuria1
- Hurler syndrome2
- Hypercholesterolemia10
- Hyperphenylalaninemia15
- Hyperthyroidism1
- Hypertriglyceridemia10
- Hypochondroplasia1
- Hypokalemic periodic paralysis2
- Hypophosphatasia195
- Hypothyroidism2
I
J
K
L
- Lactose intolerance4
- Late-onset spinal motor neuronopathy1
- LDL cholesterol4
- Leber congenital amaurosis2
- Leber's optic atrophy3
- Left1
- Leigh syndrome2
- Leprosy1
- Leukemia8
- Li-fraumeni syndrome12
- Lipoyltransferase 1 deficiency4
- Liver cancer5
- Long QT syndrome16
- Longevity14
- Lumbar disc disease4
- Lung cancer40
- Lupus25
- Lyme disease1
- Lymphoma6
- Lynch syndrome51
M
- Malaria15
- Male infertility4
- Malignant hyperthermia28
- Malignant melanoma5
- Maple syrup urine disease9
- Marfan syndrome5
- Mauriac syndrome1
- Mcardle disease1
- Medium-chain acyl-coa dehydrogenase deficiency5
- Medium-chain acyl-coenzyme a dehydrogenase deficiency1
- Medulloblastoma1
- Meier-gorlin syndrome1
- Melanoma24
- Meningioma4
- Mesothelioma1
- Metabolic syndrome2
- Metachromatic leukodystrophy3
- Migraines6
- Mitochondrial depletion syndrome31
- Mitral valve prolapse2
- MMAF4
- MNS blood group1
- Mucolipidosis type IV1
- Mucopolysaccharidosis6
- Multiple cutaneous and mucosal venous malformations3
- Multiple myeloma4
- Multiple sclerosis47
- Muscular dystrophy2
- Myasthenia gravis3
- Myelofibrosis3
- Myocardial infarction24
- Myopia4
- Myotonia congenita29
N
O
P
- Pachyonychia congenita type i9
- Pancreatic cancer13
- Panic disorder3
- Parkinson's disease77
- Pelvic organ prolapse1
- Pendred syndrome14
- Periodontitis5
- Peripheral arterial disease2
- Peripheral neuropathy1
- Peroxisome biogenesis disorder2
- Peutz-jeghers syndrome2
- Phenylketonuria256
- Photic sneeze reflex1
- Pick's disease1
- Pityriasis rubra pilaris1
- Polycystic kidney disease64
- Polycystic ovary syndrome2
- Pontocerebellar hypoplasia type 2D3
- Porphyria2
- Post-traumatic stress disorder3
- Potassium aggravated myotonia1
- Pre-eclampsia9
- Premature birth3
- Primary biliary cirrhosis4
- Primary ciliary dyskinesia1
- Primary hyperoxaluria3
- Primary sclerosing cholangitis2
- Progressive familial heart block type 1B6
- Progressive supranuclear palsy2
- Prostate cancer73
- Psoriasis23
- Psoriatic arthritis4
- PTEN hamartoma tumor syndrome2
- Pulmonary fibrosis3
R
S
- Salla disease2
- Sarcoidosis5
- Schizophrenia64
- Schwartz jampel syndrome type 12
- Sciatica1
- Scoliosis1
- Seasonal affective disorder1
- Severe combined immunodeficiency1
- Severe myoclonic epilepsy in infancy1
- Sickle cell anemia6
- Sjogren-larsson syndrome1
- Sjögren's syndrome1
- Skin cancer6
- Sleep disorder6
- Smell2
- Smith-lemli-opitz syndrome48
- Smoking12
- Social anxiety disorder3
- Spastic paraplegia7
- Speech7
- Spinal muscular atrophy22
- Spinocerebellar ataxia3
- Split hand1
- Stargardt disease3
- Stroke27
- Stuttering9
- Sudden infant death syndrome8
- Suicide5
- Sun sensitivity3
- Systemic sclerosis5
T
U
V
W
No matches.
Numbers count linked SNPs with their own page.
Source and license
Adapted from SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.