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Variant clusters
Hospitalization Episode Statistics (HES)
Genetic variants: 36,212
Diagnostic terms: × 19,155
Association results: = 693,640,860
Self-Reported Statistics (SRS)
Genetic variants: 28,458
Diagnostic terms: × 474
Association results: = 13,489,092
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Variant-specific associations

rs4360309
log Bayes Factor = 7.7722
Chromosome 8   position 126,523,523  (GRCh37) Explore rs4360309 on Ensembl!
Variant rs4360309 is listed in the   GWAS Catalog   ⇪

Hospitalization Episode Statistics (HES)

Self-Reported Statistics (SRS)
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Results table
Term Risk
posterior probability
 No effect
posterior probability
 Protective
posterior probability
  
E78.0 Pure hypercholesterolaemia
1.000 0.000 0.000
E78 Disorders of lipoprotein metabolism and other lipidaemias
0.989 0.011 0.000
E78.5 Hyperlipidaemia, unspecified
0.905 0.095 0.000
E78.8 Other disorders of lipoprotein metabolism
0.902 0.098 0.000
E78.1 Pure hyperglyceridaemia
0.885 0.115 0.000
E78.4 Other hyperlipidaemia
0.878 0.122 0.000
E78.3 Hyperchylomicronaemia
0.810 0.190 0.000
E78.6 Lipoprotein deficiency
0.785 0.215 0.000
E78.2 Mixed hyperlipidaemia
0.721 0.279 0.000
E78.9 Disorder of lipoprotein metabolism, unspecified
0.599 0.400 0.000
F31 Bipolar affective disorder
0.000 0.797 0.203
F31.9 Bipolar affective disorder, unspecified
0.000 0.807 0.193
F31.2 Bipolar affective disorder, current episode manic with psychotic symptoms
0.000 0.810 0.190
F31.1 Bipolar affective disorder, current episode manic without psychotic symptoms
0.000 0.811 0.189
F31.3 Bipolar affective disorder, current episode mild or moderate depression
0.000 0.817 0.183
F31.0 Bipolar affective disorder, current episode hypomanic
0.000 0.821 0.179
F31.7 Bipolar affective disorder, currently in remission
0.000 0.830 0.170
F31.5 Bipolar affective disorder, current episode severe depression with psychotic symptoms
0.000 0.833 0.167
F31.8 Other bipolar affective disorders
0.000 0.844 0.156
F31.4 Bipolar affective disorder, current episode severe depression without psychotic symptoms
0.000 0.851 0.148
D70 Agranulocytosis
0.118 0.882 0.000
F31.6 Bipolar affective disorder, current episode mixed
0.000 0.888 0.111
D70-D77 Other diseases of blood and blood-forming organs
0.086 0.914 0.000
C22 Malignant neoplasm of liver and intrahepatic bile ducts
0.076 0.924 0.000
C15-C26 Malignant neoplasms of digestive organs
0.074 0.926 0.000
C25 Malignant neoplasm of pancreas
0.074 0.926 0.000
C25.9 Pancreas, unspecified
0.073 0.927 0.000
C21 Malignant neoplasm of anus and anal canal
0.073 0.927 0.000
D68 Other coagulation defects
0.073 0.927 0.000
Chapter III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
0.072 0.928 0.000
C24 Malignant neoplasm of other and unspecified parts of biliary tract
0.072 0.928 0.000
D65-D69 Coagulation defects, purpura and other haemorrhagic conditions
0.071 0.929 0.000
C22.9 Liver, unspecified
0.070 0.930 0.000
D73 Diseases of spleen
0.070 0.930 0.000
C21.0 Anus, unspecified
0.070 0.930 0.000
C22.1 Intrahepatic bile duct carcinoma
0.069 0.931 0.000
C22.0 Liver cell carcinoma
0.068 0.932 0.000
C24.9 Biliary tract, unspecified
0.067 0.933 0.000
D68.2 Hereditary deficiency of other clotting factors
0.067 0.933 0.000
D68.5 Primary Thrombophilia
0.066 0.934 0.000
C21.1 Anal canal
0.066 0.934 0.000
C17 Malignant neoplasm of small intestine
0.066 0.934 0.000
D80-D89 Certain disorders involving the immune mechanism
0.065 0.935 0.000
C24.0 Extrahepatic bile duct
0.062 0.938 0.000
D74 Methaemoglobinaemia
0.062 0.938 0.000
D77 Other disorders of blood and blood-forming organs in diseases classified elsewhere
0.062 0.938 0.000
D71 Functional disorders of polymorphonuclear neutrophils
0.062 0.938 0.000
D86 Sarcoidosis
0.062 0.938 0.000
C17.0 Duodenum
0.062 0.938 0.000
D55-D59 Haemolytic anaemias
0.062 0.938 0.000
D73.3 Abscess of spleen
0.059 0.941 0.000
D86.0 Sarcoidosis of lung
0.059 0.941 0.000
C25.8 Overlapping lesion of pancreas
0.059 0.941 0.000
C25.4 Endocrine pancreas
0.059 0.941 0.000
C25.0 Head of pancreas
0.059 0.941 0.000
D73.0 Hyposplenism
0.058 0.942 0.000
D68.9 Coagulation defect, unspecified
0.058 0.942 0.000
D72 Other disorders of white blood cells
0.058 0.942 0.000
D68.4 Acquired coagulation factor deficiency
0.058 0.942 0.000
D73.9 Disease of spleen, unspecified
0.058 0.942 0.000
D68.3 Haemorrhagic disorder due to circulating anticoagulants
0.058 0.942 0.000
D67 Hereditary factor IX deficiency
0.057 0.943 0.000
C26 Malignant neoplasm of other and ill-defined digestive organs
0.056 0.944 0.000
C22.7 Other specified carcinomas of liver
0.055 0.945 0.000
C22.4 Other sarcomas of liver
0.055 0.945 0.000
C22.3 Angiosarcoma of liver
0.055 0.945 0.000
C22.2 Hepatoblastoma
0.055 0.945 0.000
D58 Other hereditary haemolytic anaemias
0.055 0.945 0.000
C24.1 Ampulla of Vater
0.053 0.946 0.000
D76 Certain diseases involving lymphoreticular tissue and reticulohistiocytic system
0.053 0.946 0.000
C23 Malignant neoplasm of gallbladder
0.053 0.946 0.000
D68.8 Other specified coagulation defects
0.053 0.947 0.000
D86.8 Sarcoidosis of other and combined sites
0.053 0.947 0.000
C21.2 Cloacogenic zone
0.053 0.947 0.000
D66 Hereditary factor VIII deficiency
0.053 0.947 0.000
D68.1 Hereditary factor XI deficiency
0.052 0.948 0.000
C24.8 Overlapping lesion of biliary tract
0.052 0.948 0.000
D68.6 Other Thrombophilia
0.051 0.948 0.000
C25.7 Other parts of pancreas
0.051 0.949 0.000
C25.1 Body of pancreas
0.051 0.949 0.000
D80 Immunodeficiency with predominantly antibody defects
0.051 0.949 0.000
D65 Disseminated intravascular coagulation [defibrination syndrome]
0.051 0.949 0.000
C25.3 Pancreatic duct
0.051 0.949 0.000
D73.2 Chronic congestive splenomegaly
0.050 0.949 0.000
D57 Sickle-cell disorders
0.050 0.950 0.000
C17.2 Ileum
0.049 0.951 0.000
C21.8 Overlapping lesion of rectum, anus and anal canal
0.048 0.952 0.000
C17.8 Overlapping lesion of small intestine
0.047 0.953 0.000
C17.3 Meckel's diverticulum
0.047 0.953 0.000
D58.9 Hereditary haemolytic anaemia, unspecified
0.047 0.953 0.000
D68.0 Von Willebrand's disease
0.047 0.953 0.000
C17.1 Jejunum
0.047 0.953 0.000
C16 Malignant neoplasm of stomach
0.047 0.953 0.000
D81 Combined immunodeficiencies
0.047 0.953 0.000
D75 Other diseases of blood and blood-forming organs
0.047 0.953 0.000
D73.5 Infarction of spleen
0.046 0.953 0.000
D73.8 Other diseases of spleen
0.046 0.954 0.000
D58.0 Hereditary spherocytosis
0.046 0.954 0.000
D73.1 Hypersplenism
0.046 0.954 0.000
D59 Acquired haemolytic anaemia
0.046 0.954 0.000
C19 Malignant neoplasm of rectosigmoid junction
0.046 0.954 0.000
D84 Other immunodeficiencies
0.045 0.955 0.000
D74.9 Methaemoglobinaemia, unspecified
0.044 0.955 0.000
D74.8 Other methaemoglobinaemias
0.044 0.955 0.000
D74.0 Congenital methaemoglobinaemia
0.044 0.955 0.000
C25.2 Tail of pancreas
0.044 0.955 0.000
D55 Anaemia due to enzyme disorders
0.044 0.955 0.000
D86.2 Sarcoidosis of lung with sarcoidosis of lymph nodes
0.044 0.955 0.000
D72.8 Other specified disorders of white blood cells
0.044 0.956 0.000
D82 Immunodeficiency associated with other major defects
0.044 0.956 0.000
D86.9 Sarcoidosis, unspecified
0.044 0.956 0.000
D80.9 Immunodeficiency with predominantly antibody defects, unspecified
0.043 0.957 0.000
C26.0 Intestinal tract, part unspecified
0.043 0.957 0.000
D89 Other disorders involving the immune mechanism, not elsewhere classified
0.043 0.957 0.000
C16.2 Body of stomach
0.043 0.957 0.000
D72.9 Disorder of white blood cells, unspecified
0.042 0.958 0.000
D72.0 Genetic anomalies of leukocytes
0.042 0.958 0.000
D83 Common variable immunodeficiency
0.041 0.958 0.000
D57.1 Sickle-cell anaemia without crisis
0.041 0.959 0.000
C26.9 Ill-defined sites within the digestive system
0.041 0.959 0.000
D86.3 Sarcoidosis of skin
0.041 0.959 0.000
D86.1 Sarcoidosis of lymph nodes
0.041 0.959 0.000
C26.8 Overlapping lesion of digestive system
0.041 0.959 0.000
C26.1 Spleen
0.041 0.959 0.000
D73.4 Cyst of spleen
0.040 0.960 0.000
D80.6 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia
0.040 0.960 0.000
C15 Malignant neoplasm of oesophagus
0.039 0.960 0.000
D58.8 Other specified hereditary haemolytic anaemias
0.039 0.961 0.000
D58.1 Hereditary elliptocytosis
0.039 0.961 0.000
D80.1 Nonfamilial hypogammaglobulinaemia
0.039 0.961 0.000
D76.2 Haemophagocytic syndrome, infection-associated
0.038 0.961 0.000
D76.1 Haemophagocytic lymphohistiocytosis
0.038 0.961 0.000
D76.0 Langerhans' cell histiocytosis, not elsewhere classified
0.038 0.961 0.000
D75.8 Other specified diseases of blood and blood-forming organs
0.038 0.962 0.000
D80.3 Selective deficiency of immunoglobulin G [IgG] subclasses
0.038 0.962 0.000
D75.2 Essential thrombocytosis
0.038 0.962 0.000
D84.1 Defects in the complement system
0.037 0.962 0.000
D89.8 Other specified disorders involving the immune mechanism, not elsewhere classified
0.037 0.963 0.000
D59.0 Drug-induced autoimmune haemolytic anaemia
0.037 0.963 0.000
D80.8 Other immunodeficiencies with predominantly antibody defects
0.037 0.963 0.000
D80.7 Transient hypogammaglobulinaemia of infancy
0.037 0.963 0.000
D80.5 Immunodeficiency with increased immunoglobulin M [IgM]
0.037 0.963 0.000
D80.0 Hereditary hypogammaglobulinaemia
0.037 0.963 0.000
C16.6 Greater curvature of stomach, unspecified
0.036 0.964 0.000
D57.8 Other sickle-cell disorders
0.036 0.964 0.000
D57.3 Sickle-cell trait
0.036 0.964 0.000
D57.2 Double heterozygous sickling disorders
0.036 0.964 0.000
D57.0 Sickle-cell anaemia with crisis
0.036 0.964 0.000
D58.2 Other haemoglobinopathies
0.036 0.964 0.000
Z95.2 Presence of prosthetic heart valve
0.036 0.964 0.000
C17.9 Small intestine, unspecified
0.035 0.964 0.000
D72.1 Eosinophilia
0.035 0.965 0.000
D69 Purpura and other haemorrhagic conditions
0.034 0.966 0.000
D80.4 Selective deficiency of immunoglobulin M [IgM]
0.034 0.966 0.000
D81.9 Combined immunodeficiency, unspecified
0.034 0.966 0.000
D81.8 Other combined immunodeficiencies
0.034 0.966 0.000
D81.7 Major histocompatibility complex class II deficiency
0.034 0.966 0.000
D81.6 Major histocompatibility complex class I deficiency
0.034 0.966 0.000
D81.5 Purine nucleoside phosphorylase [PNP] deficiency
0.034 0.966 0.000
D81.4 Nezelof's syndrome
0.034 0.966 0.000
D81.3 Adenosine deaminase [ADA] deficiency
0.034 0.966 0.000
D81.2 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
0.034 0.966 0.000
D81.1 Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
0.034 0.966 0.000
D81.0 Severe combined immunodeficiency [SCID] with reticular dysgenesis
0.034 0.966 0.000
C16.8 Overlapping lesion of stomach
0.034 0.966 0.000
D56 Thalassaemia
0.033 0.966 0.000
C15.3 Upper third of oesophagus
0.034 0.966 0.000
D75.0 Familial erythrocytosis
0.033 0.967 0.000
D59.8 Other acquired haemolytic anaemias
0.033 0.967 0.000
D59.6 Haemoglobinuria due to haemolysis from other external causes
0.033 0.967 0.000
D59.5 Paroxysmal nocturnal haemoglobinuria [Marchiafava-Micheli]
0.033 0.967 0.000
D59.4 Other nonautoimmune haemolytic anaemias
0.033 0.967 0.000
D59.3 Haemolytic-uraemic syndrome
0.033 0.967 0.000
D59.2 Drug-induced nonautoimmune haemolytic anaemia
0.033 0.967 0.000
D84.0 Lymphocyte function antigen-1 [LFA-1] defect
0.033 0.967 0.000
C16.4 Pylorus
0.033 0.967 0.000
C16.3 Pyloric antrum
0.033 0.967 0.000
C16.5 Lesser curvature of stomach, unspecified
0.033 0.967 0.000
D55.9 Anaemia due to enzyme disorder, unspecified
0.032 0.968 0.000
D55.8 Other anaemias due to enzyme disorders
0.032 0.968 0.000
D55.3 Anaemia due to disorders of nucleotide metabolism
0.032 0.968 0.000
D55.2 Anaemia due to disorders of glycolytic enzymes
0.032 0.968 0.000
D55.1 Anaemia due to other disorders of glutathione metabolism
0.032 0.968 0.000
D55.0 Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
0.032 0.968 0.000
D59.9 Acquired haemolytic anaemia, unspecified
0.032 0.968 0.000
D59.1 Other autoimmune haemolytic anaemias
0.032 0.968 0.000
D82.9 Immunodeficiency associated with major defect, unspecified
0.031 0.968 0.000
D82.8 Immunodeficiency associated with other specified major defects
0.031 0.968 0.000
D82.4 Hyperimmunoglobulin E [IgE] syndrome
0.031 0.968 0.000
D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus
0.031 0.968 0.000
D82.2 Immunodeficiency with short-limbed stature
0.031 0.968 0.000
D82.0 Wiskott-Aldrich syndrome
0.031 0.968 0.000
C16.1 Fundus of stomach
0.031 0.969 0.000
D89.3 Immune reconstitution syndrome
0.031 0.969 0.000
D76.3 Other histiocytosis syndromes
0.030 0.970 0.000
D83.8 Other common variable immunodeficiencies
0.030 0.970 0.000
D83.2 Common variable immunodeficiency with autoantibodies to B- or T-cells
0.030 0.970 0.000
D83.1 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
0.030 0.970 0.000
D83.0 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
0.030 0.970 0.000
D60-D64 Aplastic and other anaemias
0.030 0.970 0.000
C15.0 Cervical part of oesophagus
0.029 0.970 0.000
D69.5 Secondary thrombocytopenia
0.029 0.971 0.000
C16.9 Stomach, unspecified
0.029 0.971 0.000
D82.1 Di George's syndrome
0.029 0.971 0.000
D84.8 Other specified immunodeficiencies
0.028 0.971 0.000
D84.9 Immunodeficiency, unspecified
0.028 0.971 0.000
C15.8 Overlapping lesion of oesophagus
0.028 0.971 0.000
C15.2 Abdominal part of oesophagus
0.028 0.971 0.000
D89.1 Cryoglobulinaemia
0.028 0.972 0.000
D89.0 Polyclonal hypergammaglobulinaemia
0.028 0.972 0.000
D89.9 Disorder involving the immune mechanism, unspecified
0.028 0.972 0.000
D61 Other aplastic anaemias
0.028 0.972 0.000
C15.4 Middle third of oesophagus
0.028 0.972 0.000
D80.2 Selective deficiency of immunoglobulin A [IgA]
0.027 0.972 0.000
F30-F39 Mood [affective] disorders
0.000 0.973 0.027
D69.8 Other specified haemorrhagic conditions
0.026 0.974 0.000
D69.3 Idiopathic thrombocytopenic purpura
0.026 0.974 0.000
C15.9 Oesophagus, unspecified
0.026 0.974 0.000
C15.1 Thoracic part of oesophagus
0.025 0.975 0.000
D83.9 Common variable immunodeficiency, unspecified
0.025 0.975 0.000
D89.2 Hypergammaglobulinaemia, unspecified
0.025 0.975 0.000
D61.9 Aplastic anaemia, unspecified
0.025 0.975 0.000
D69.4 Other primary thrombocytopenia
0.024 0.975 0.000
D61.1 Drug-induced aplastic anaemia
0.024 0.976 0.000
D56.9 Thalassaemia, unspecified
0.024 0.976 0.000
D56.8 Other thalassaemias
0.024 0.976 0.000
D56.4 Hereditary persistence of foetal haemoglobin [HPFH]
0.024 0.976 0.000
D56.2 Delta-beta thalassaemia
0.024 0.976 0.000
D56.0 Alpha thalassaemia
0.024 0.976 0.000
D69.2 Other nonthrombocytopenic purpura
0.023 0.977 0.000
D69.1 Qualitative platelet defects
0.022 0.977 0.000
D75.9 Disease of blood and blood-forming organs, unspecified
0.022 0.978 0.000
D56.1 Beta thalassaemia
0.022 0.978 0.000
R50.9 Fever, unspecified
0.022 0.978 0.000
D60 Acquired pure red cell aplasia [erythroblastopenia]
0.020 0.980 0.000
D61.8 Other specified aplastic anaemias
0.020 0.980 0.000
D61.3 Idiopathic aplastic anaemia
0.020 0.980 0.000
D61.2 Aplastic anaemia due to other external agents
0.020 0.980 0.000
D69.9 Haemorrhagic condition, unspecified
0.020 0.980 0.000
D61.0 Constitutional aplastic anaemia
0.020 0.980 0.000
F38 Other mood [affective] disorders
0.000 0.980 0.020
F34 Persistent mood [affective] disorders
0.000 0.980 0.020
N64.1 Fat necrosis of breast
0.018 0.982 0.000
D69.0 Allergic purpura
0.017 0.982 0.000
F39 Unspecified mood [affective] disorder
0.000 0.983 0.017
D56.3 Thalassaemia trait
0.017 0.983 0.001
C16.0 Cardia
0.016 0.984 0.000
R50 Fever of unknown origin
0.016 0.984 0.000
F34.1 Dysthymia
0.000 0.984 0.016
F32 Depressive episode
0.000 0.984 0.016
F30 Manic episode
0.000 0.985 0.015
N64 Other disorders of breast
0.015 0.985 0.000
R50.0 Fever with chills
0.015 0.985 0.000
J15.1 Pneumonia due to Pseudomonas
0.015 0.985 0.000
N64.5 Other signs and symptoms in breast
0.015 0.985 0.000
D60.8 Other acquired pure red cell aplasias
0.015 0.985 0.000
D60.1 Transient acquired pure red cell aplasia
0.015 0.985 0.000
D60.0 Chronic acquired pure red cell aplasia
0.015 0.985 0.000
F38.8 Other specified mood [affective] disorders
0.000 0.985 0.015
F38.0 Other single mood [affective] disorders
0.000 0.985 0.014
J15 Bacterial pneumonia, not elsewhere classified
0.015 0.985 0.000
F38.1 Other recurrent mood [affective] disorders
0.000 0.986 0.014
F34.9 Persistent mood [affective] disorder, unspecified
0.000 0.986 0.014
F34.8 Other persistent mood [affective] disorders
0.000 0.986 0.014
D62 Acute posthaemorrhagic anaemia
0.014 0.986 0.000
F32.0 Mild depressive episode
0.000 0.986 0.014
D60.9 Acquired pure red cell aplasia, unspecified
0.014 0.986 0.000
J15.4 Pneumonia due to other streptococci
0.013 0.986 0.000
F34.0 Cyclothymia
0.000 0.987 0.013
R50.8 Other specified fever
0.013 0.987 0.000
F32.1 Moderate depressive episode
0.000 0.987 0.013
N64.9 Disorder of breast, unspecified
0.013 0.987 0.000
R50.2 Drug-induced fever
0.013 0.987 0.000
D50-D53 Nutritional anaemias
0.012 0.988 0.000
N64.4 Mastodynia
0.012 0.988 0.000
J15.2 Pneumonia due to staphylococcus
0.012 0.988 0.000
J15.9 Bacterial pneumonia, unspecified
0.012 0.988 0.000
D75.1 Secondary polycythaemia
0.012 0.988 0.000
S68.1 Traumatic amputation of other single finger (complete)(partial)
0.000 0.988 0.012
J15.7 Pneumonia due to Mycoplasma pneumoniae
0.012 0.988 0.000
D64 Other anaemias
0.012 0.988 0.000
F33 Recurrent depressive disorder
0.000 0.989 0.011
D69.6 Thrombocytopenia, unspecified
0.011 0.989 0.000
F30.8 Other manic episodes
0.000 0.989 0.011
F30.1 Mania without psychotic symptoms
0.000 0.989 0.011
N64.0 Fissure and fistula of nipple
0.011 0.989 0.000
J15.0 Pneumonia due to Klebsiella pneumoniae
0.011 0.989 0.000
J15.8 Other bacterial pneumonia
0.011 0.989 0.000
N64.2 Atrophy of breast
0.011 0.989 0.000
J15.5 Pneumonia due to Escherichia coli
0.011 0.989 0.000
F30.0 Hypomania
0.000 0.989 0.011
C15.5 Lower third of oesophagus
0.011 0.989 0.000
N64.3 Galactorrhoea not associated with childbirth
0.011 0.989 0.000
J15.3 Pneumonia due to streptococcus, group B
0.011 0.989 0.000
J15.6 Pneumonia due to other aerobic Gram-negative bacteria
0.011 0.989 0.000
F30.2 Mania with psychotic symptoms
0.000 0.989 0.010
F32.3 Severe depressive episode with psychotic symptoms
0.000 0.990 0.010
F32.8 Other depressive episodes
0.000 0.990 0.010
N64.8 Other specified disorders of breast
0.010 0.990 0.000
F33.1 Recurrent depressive disorder, current episode moderate
0.000 0.990 0.010
F32.2 Severe depressive episode without psychotic symptoms
0.000 0.990 0.010
F33.0 Recurrent depressive disorder, current episode mild
0.000 0.991 0.009
D64.3 Other sideroblastic anaemias
0.009 0.991 0.000
E88.0 Disorders of plasma-protein metabolism, not elsewhere classified
0.009 0.991 0.000
R50.1 Persistent fever
0.009 0.991 0.000
F33.4 Recurrent depressive disorder, currently in remission
0.000 0.991 0.009
F30.9 Manic episode, unspecified
0.000 0.991 0.009
S52.10 Fracture of upper end of radius (closed)
0.000 0.991 0.009
D64.4 Congenital dyserythropoietic anaemia
0.008 0.991 0.000
D64.2 Secondary sideroblastic anaemia due to drugs and toxins
0.008 0.991 0.000
D64.1 Secondary sideroblastic anaemia due to disease
0.008 0.991 0.000
D64.0 Hereditary sideroblastic anaemia
0.008 0.991 0.000
I49.8 Other specified cardiac arrhythmias
0.000 0.992 0.008
D52 Folate deficiency anaemia
0.008 0.992 0.000
F33.8 Other recurrent depressive disorders
0.000 0.992 0.008
Z41.1 Other plastic surgery for unacceptable cosmetic appearance
0.008 0.992 0.000
D53 Other nutritional anaemias
0.007 0.992 0.000
E88 Other metabolic disorders
0.007 0.992 0.000
D64.8 Other specified anaemias
0.007 0.993 0.000
D63 Anaemia in chronic diseases classified elsewhere
0.007 0.993 0.000
I49.9 Cardiac arrhythmia, unspecified
0.000 0.993 0.007
K75.0 Abscess of liver
0.007 0.993 0.000
J10 Influenza due to identified influenza virus
0.007 0.993 0.000
E70-E90 Metabolic disorders
0.007 0.993 0.000
J09-J18 Influenza and pneumonia
0.007 0.993 0.000
F33.2 Recurrent depressive disorder, current episode severe without psychotic symptoms
0.000 0.993 0.006
E88.3 Tumour lysis syndrome
0.006 0.994 0.000
J10.1 Influenza with other respiratory manifestations, influenza virus identified
0.006 0.994 0.000
I49 Other cardiac arrhythmias
0.000 0.994 0.006
N85.1 Endometrial adenomatous hyperplasia
0.006 0.994 0.000
I49.5 Sick sinus syndrome
0.000 0.994 0.006
D52.8 Other folate deficiency anaemias
0.006 0.994 0.000
D52.1 Drug-induced folate deficiency anaemia
0.006 0.994 0.000
D52.0 Dietary folate deficiency anaemia
0.006 0.994 0.000
J17 Pneumonia in diseases classified elsewhere
0.006 0.994 0.000
E88.2 Lipomatosis, not elsewhere classified
0.006 0.994 0.000
F33.3 Recurrent depressive disorder, current episode severe with psychotic symptoms
0.000 0.994 0.006
J10.0 Influenza with pneumonia, influenza virus identified
0.006 0.994 0.000
D53.8 Other specified nutritional anaemias
0.005 0.994 0.000
D53.2 Scorbutic anaemia
0.005 0.994 0.000
D53.0 Protein deficiency anaemia
0.005 0.994 0.000
M77.02 Medial epicondylitis (Upper arm)
0.006 0.994 0.000
E70 Disorders of aromatic amino-acid metabolism
0.005 0.994 0.000
D63.1 Anaemia in other chronic diseases classified elsewhere
0.005 0.995 0.000
D53.1 Other megaloblastic anaemias, not elsewhere classified
0.005 0.995 0.000
E88.8 Other specified metabolic disorders
0.005 0.995 0.000
D51 Vitamin B12 deficiency anaemia
0.005 0.995 0.000
J12 Viral pneumonia, not elsewhere classified
0.005 0.995 0.000
E79 Disorders of purine and pyrimidine metabolism
0.005 0.995 0.000
J17.1 Pneumonia in viral diseases classified elsewhere
0.005 0.995 0.000
J10.8 Influenza with other manifestations, influenza virus identified
0.005 0.995 0.000
E77 Disorders of glycoprotein metabolism
0.005 0.995 0.000
E76 Disorders of glycosaminoglycan metabolism
0.005 0.995 0.000
E71 Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
0.005 0.995 0.000
E90 Nutritional and metabolic disorders in diseases classified elsewhere
0.005 0.995 0.000
J16 Pneumonia due to other infectious organisms, not elsewhere classified
0.005 0.995 0.000
J09 Influenza due to certain identified influenza virus
0.005 0.995 0.000
E72 Other disorders of amino-acid metabolism
0.005 0.995 0.000
E88.1 Lipodystrophy, not elsewhere classified
0.005 0.995 0.000
D52.9 Folate deficiency anaemia, unspecified
0.005 0.995 0.000
J17.2 Pneumonia in mycoses
0.005 0.995 0.000
I49.2 Junctional premature depolarisation
0.000 0.995 0.005
E74 Other disorders of carbohydrate metabolism
0.005 0.995 0.000
E70.3 Albinism
0.005 0.995 0.000
I49.3 Ventricular premature depolarisation
0.000 0.995 0.005
E84 Cystic fibrosis
0.005 0.995 0.000
E75 Disorders of sphingolipid metabolism and other lipid storage disorders
0.004 0.995 0.000
D53.9 Nutritional anaemia, unspecified
0.004 0.995 0.000
E88.9 Metabolic disorder, unspecified
0.004 0.995 0.000
J13 Pneumonia due to Streptococcus pneumoniae
0.005 0.995 0.000
I61.0 Intracerebral haemorrhage in hemisphere, subcortical
0.005 0.995 0.000
J17.8 Pneumonia in other diseases classified elsewhere
0.004 0.996 0.000
J11 Influenza, virus not identified
0.004 0.996 0.000
S68 Traumatic amputation of wrist and hand
0.000 0.996 0.004
J17.3 Pneumonia in parasitic diseases
0.004 0.996 0.000
J17.0 Pneumonia in bacterial diseases classified elsewhere
0.004 0.996 0.000
J12.1 Respiratory syncytial virus pneumonia
0.004 0.996 0.000
E70.9 Disorder of aromatic amino-acid metabolism, unspecified
0.004 0.996 0.000
E70.8 Other disorders of aromatic amino-acid metabolism
0.004 0.996 0.000
E70.2 Disorders of tyrosine metabolism
0.004 0.996 0.000
E70.1 Other hyperphenylalaninaemias
0.004 0.996 0.000
E70.0 Classical phenylketonuria
0.004 0.996 0.000
I61.9 Intracerebral haemorrhage, unspecified
0.004 0.996 0.000
I61 Intracerebral haemorrhage
0.004 0.996 0.000
E73 Lactose intolerance
0.004 0.996 0.000
D51.8 Other vitamin B12 deficiency anaemias
0.004 0.996 0.000
D51.3 Other dietary vitamin B12 deficiency anaemia
0.004 0.996 0.000
J12.2 Parainfluenza virus pneumonia
0.004 0.996 0.000
E79.0 Hyperuricaemia without signs of inflammatory arthritis and tophaceous disease
0.004 0.996 0.000
T90.2 Sequelae of fracture of skull and facial bones
0.004 0.996 0.000
I49.0 Ventricular fibrillation and flutter
0.000 0.996 0.004
D25.1 Intramural leiomyoma of uterus
0.004 0.996 0.000
D51.2 Transcobalamin II deficiency
0.004 0.996 0.000
D51.1 Vitamin B12 deficiency anaemia due to selective vitamin B12 malabsorption with proteinuria
0.004 0.996 0.000
E79.9 Disorder of purine and pyrimidine metabolism, unspecified
0.004 0.996 0.000
E79.8 Other disorders of purine and pyrimidine metabolism
0.004 0.996 0.000
E79.1 Lesch-Nyhan syndrome
0.004 0.996 0.000
J12.8 Other viral pneumonia
0.004 0.996 0.000
J12.3 Human metapneumovirus pneumonia
0.004 0.996 0.000
J12.0 Adenoviral pneumonia
0.004 0.996 0.000
E71.3 Disorders of fatty-acid metabolism
0.004 0.996 0.000
E71.2 Disorder of branched-chain amino-acid metabolism, unspecified
0.004 0.996 0.000
E71.1 Other disorders of branched-chain amino-acid metabolism
0.004 0.996 0.000
E71.0 Maple-syrup-urine disease
0.004 0.996 0.000
E76.9 Disorder of glucosaminoglycan metabolism, unspecified
0.004 0.996 0.000
E76.8 Other disorders of glucosaminoglycan metabolism
0.004 0.996 0.000
E76.3 Mucopolysaccharidosis, unspecified
0.004 0.996 0.000
E76.2 Other mucopolysaccharidoses
0.004 0.996 0.000
E76.1 Mucopolysaccharidosis, type II
0.004 0.996 0.000
E76.0 Mucopolysaccharidosis, type I
0.004 0.996 0.000
E77.9 Disorder of glycoprotein metabolism, unspecified
0.004 0.996 0.000
E77.8 Other disorders of glycoprotein metabolism
0.004 0.996 0.000
E77.1 Defects in glycoprotein degradation
0.004 0.996 0.000
E77.0 Defects in posttranslational modification of lysosomal enzymes
0.004 0.996 0.000
J16.8 Pneumonia due to other specified infectious organisms
0.004 0.996 0.000
J16.0 Chlamydial pneumonia
0.004 0.996 0.000
E72.9 Disorder of amino-acid metabolism, unspecified
0.004 0.996 0.000
E72.8 Other specified disorders of amino-acid metabolism
0.004 0.996 0.000
E72.5 Disorders of glycine metabolism
0.004 0.996 0.000
E72.4 Disorders of ornithine metabolism
0.004 0.996 0.000
E72.3 Disorders of lysine and hydroxylysine metabolism
0.004 0.996 0.000
E72.2 Disorders of urea cycle metabolism
0.004 0.996 0.000
B99 Other and unspecified infectious diseases
0.004 0.996 0.000
E72.1 Disorders of sulphur-bearing amino-acid metabolism
0.004 0.996 0.000
E72.0 Disorders of amino-acid transport
0.004 0.996 0.000
I49.4 Other and unspecified premature depolarisation
0.000 0.996 0.004
J11.8 Influenza with other manifestations, virus not identified
0.004 0.996 0.000
I61.2 Intracerebral haemorrhage in hemisphere, unspecified
0.004 0.996 0.000
I61.1 Intracerebral haemorrhage in hemisphere, cortical
0.004 0.996 0.000
M77.0 Medial epicondylitis
0.004 0.996 0.000
E85 Amyloidosis
0.004 0.996 0.000
E74.9 Disorder of carbohydrate metabolism, unspecified
0.004 0.996 0.000
E74.8 Other specified disorders of carbohydrate metabolism
0.004 0.996 0.000
E74.4 Disorders of pyruvate metabolism and gluconeogenesis
0.004 0.996 0.000
E74.2 Disorders of galactose metabolism
0.004 0.996 0.000
E74.1 Disorders of fructose metabolism
0.004 0.996 0.000
E74.0 Glycogen storage disease
0.004 0.996 0.000
I61.6 Intracerebral haemorrhage, multiple localised
0.004 0.996 0.000
I61.4 Intracerebral haemorrhage in cerebellum
0.004 0.996 0.000
I33.0 Acute and subacute infective endocarditis
0.004 0.996 0.000
I49.1 Atrial premature depolarisation
0.000 0.996 0.004
G35 Multiple sclerosis
0.000 0.996 0.004
J12.9 Viral pneumonia, unspecified
0.003 0.996 0.000
E84.8 Cystic fibrosis with other manifestations
0.003 0.996 0.000
E84.1 Cystic fibrosis with intestinal manifestations
0.003 0.996 0.000
E84.0 Cystic fibrosis with pulmonary manifestations
0.003 0.996 0.000
E75.6 Lipid storage disorder, unspecified
0.003 0.996 0.000
E75.4 Neuronal ceroid lipofuscinosis
0.003 0.996 0.000
E75.3 Sphingolipidosis, unspecified
0.003 0.996 0.000
E75.1 Other gangliosidosis
0.003 0.996 0.000
E75.0 GM2 gangliosidosis
0.003 0.996 0.000
Y46.6 Other and unspecified antiepileptics
0.004 0.996 0.000
Y46 Antiepileptics and anti-Parkinsonism drugs
0.003 0.996 0.000
E74.3 Other disorders of intestinal carbohydrate absorption
0.003 0.997 0.000
S68.9 Traumatic amputation of wrist and hand, level unspecified
0.000 0.997 0.003
S68.8 Traumatic amputation of other parts of wrist and hand
0.000 0.997 0.003
S68.4 Traumatic amputation of hand at wrist level
0.000 0.997 0.003
S68.3 Combined traumatic amputation of (part of) finger(s) with other parts of wrist and hand
0.000 0.997 0.003
S52.1 Fracture of upper end of radius
0.000 0.997 0.003
E75.2 Other sphingolipidosis
0.003 0.997 0.000
S68.2 Traumatic amputation of two or more fingers alone (complete)(partial)
0.000 0.997 0.003
Y46.4 Iminostilbenes
0.003 0.997 0.000
F33.9 Recurrent depressive disorder, unspecified
0.000 0.997 0.003
I31.9 Disease of pericardium, unspecified
0.003 0.997 0.000
J11.0 Influenza with pneumonia, virus not identified
0.003 0.997 0.000
N48.1 Balanoposthitis
0.000 0.997 0.003
E75.5 Other lipid storage disorders
0.003 0.997 0.000
W02.9 Unspecified place
0.000 0.997 0.003
Y46.2 Hydantoin derivatives
0.003 0.997 0.000
E73.8 Other lactose intolerance
0.003 0.997 0.000
E73.1 Secondary lactase deficiency
0.003 0.997 0.000
E73.0 Congenital lactase deficiency
0.003 0.997 0.000
J18 Pneumonia, organism unspecified
0.003 0.997 0.000
Z41 Procedures for purposes other than remedying health state
0.003 0.997 0.000
E84.9 Cystic fibrosis, unspecified
0.003 0.997 0.000
D51.9 Vitamin B12 deficiency anaemia, unspecified
0.003 0.997 0.000
S68.0 Traumatic amputation of thumb (complete)(partial)
0.000 0.997 0.003
Y46.5 Valproic acid
0.003 0.997 0.000
I61.8 Other intracerebral haemorrhage
0.003 0.997 0.000
M77.09 Medial epicondylitis (Site unspecified)
0.003 0.997 0.000
M77.08 Medial epicondylitis-Other
0.003 0.997 0.000
M77.07 Medial epicondylitis-Ankle/Foot
0.003 0.997 0.000
M77.06 Medial epicondylitis (Lower leg)
0.003 0.997 0.000
M77.05 Medial epicondylitis (Pelvic region and thigh)
0.003 0.997 0.000
M77.04 Medial epicondylitis-Hand
0.003 0.997 0.000
M77.03 Medial epicondylitis-Forearm
0.003 0.997 0.000
M77.01 Medial epicondylitis-Shldr region
0.003 0.997 0.000
M77.00 Medial epicondylitis (Multiple sites)
0.003 0.997 0.000
R25.2 Cramp and spasm
0.003 0.997 0.000
R29.6 Tendency to fall, not elsewhere classified
0.003 0.997 0.000
J14 Pneumonia due to Haemophilus influenzae
0.003 0.997 0.000
E85.2 Heredofamilial amyloidosis, unspecified
0.003 0.997 0.000
E85.1 Neuropathic heredofamilial amyloidosis
0.003 0.997 0.000
E85.0 Nonneuropathic heredofamilial amyloidosis
0.003 0.997 0.000
E85.8 Other amyloidosis
0.003 0.997 0.000
K75 Other inflammatory liver diseases
0.003 0.997 0.000
M48.02 Spinal stenosis (Cervical region)
0.003 0.997 0.000
E85.9 Amyloidosis, unspecified
0.003 0.997 0.000
N13.1 Hydronephrosis with ureteral stricture, not elsewhere classified
0.003 0.997 0.000
Z41.9 Procedures for purposes other than remedying health state, unspecified
0.003 0.997 0.000

This table lists the top 500 terms ordered by p(effect).

The full results table can be downloaded from this page.

 

The TreeWAS Database is the result of research conducted at the Oxford Big Data Institute at the University of Oxford.

This research has been conducted using the UK Biobank Resource (application number 10625). This work uses data provided by patients and collected by the NHS as part of their care and support.

This research has been conducted with the support of the Wellcome Trust (100956/Z/13/Z and 090532/Z/09/Z and 100308/Z/12/Z), the Danish National Research Foundation, Takeda, the Medical Research Council (MC_UU_12010/3), the Oak Foundation (OCAY-15-520), the National Institute for Health Research (NIHR) Oxford Biomedical Research Centre (BRC), the Wellcome Trust/Royal Society (204290/Z/16/Z) and the Li Ka Shing Foundation.

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