TreeWAS – Variant ID: rs1943466

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
D12.5 Sigmoid colon	0.822	0.178	0.000
D12 Benign neoplasm of colon, rectum, anus and anal canal	0.786	0.214	0.000
D12.0 Caecum	0.757	0.243	0.000
D12.2 Ascending colon	0.741	0.259	0.000
D12.4 Descending colon	0.691	0.309	0.000
D12.3 Transverse colon	0.685	0.315	0.000
D12.7 Rectosigmoid junction	0.544	0.456	0.000
D12.9 Anus and anal canal	0.536	0.464	0.000
D12.8 Rectum	0.454	0.546	0.000
D12.1 Appendix	0.437	0.562	0.000
D12.6 Colon, unspecified	0.278	0.722	0.000
D11.0 Parotid gland	0.092	0.908	0.000
M79.60 Pain in limb (Multiple sites)	0.000	0.946	0.054
D11 Benign neoplasm of major salivary glands	0.025	0.975	0.000
D11.9 Major salivary gland, unspecified	0.017	0.983	0.000
D11.7 Other major salivary glands	0.013	0.986	0.000
C02.9 Tongue, unspecified	0.011	0.989	0.000
Z08.2 Follow-up examination after chemotherapy for malignant neoplasm	0.011	0.989	0.000
C02 Malignant neoplasm of other and unspecified parts of tongue	0.009	0.991	0.000
M19.17 Post-traumatic arthrosis of other joints (Ankle and foot)	0.008	0.992	0.000
C02.2 Ventral surface of tongue	0.008	0.992	0.000
H72.9 Perforation of tympanic membrane, unspecified	0.000	0.993	0.007
C02.4 Lingual tonsil	0.007	0.993	0.000
N83.1 Corpus luteum cyst	0.007	0.993	0.000
C02.8 Overlapping lesion of tongue	0.006	0.993	0.000
C02.3 Anterior two-thirds of tongue, part unspecified	0.006	0.993	0.000
C02.0 Dorsal surface of tongue	0.006	0.993	0.000
Z36.0 Antenatal screening for chromosomal anomalies	0.000	0.994	0.006
C83.3 Large cell (diffuse)	0.000	0.994	0.006
C00-C14 Malignant neoplasms of lip, oral cavity and pharynx	0.006	0.994	0.000
C02.1 Border of tongue	0.005	0.994	0.000
Z93.0 Tracheostomy status	0.000	0.994	0.006
C06 Malignant neoplasm of other and unspecified parts of mouth	0.005	0.994	0.000
R93.3 Abnormal findings on diagnostic imaging of other parts of digestive tract	0.005	0.995	0.000
K75.8 Other specified inflammatory liver diseases	0.005	0.995	0.000
D89.2 Hypergammaglobulinaemia, unspecified	0.000	0.995	0.005
M19.1 Posttraumatic arthrosis of other joints	0.005	0.995	0.000
L85.9 Epidermal thickening, unspecified	0.005	0.995	0.000
Z36.8 Other antenatal screening	0.000	0.995	0.005
C06.0 Cheek mucosa	0.005	0.995	0.000
C10 Malignant neoplasm of oropharynx	0.005	0.995	0.000
C05 Malignant neoplasm of palate	0.005	0.995	0.000
Q66.8 Other congenital deformities of feet	0.005	0.995	0.000
C06.2 Retromolar area	0.005	0.995	0.000
Q66 Congenital deformities of feet	0.005	0.995	0.000
Z36 Antenatal screening	0.000	0.995	0.005
C12 Malignant neoplasm of pyriform sinus	0.005	0.995	0.000
H54.4 Blindness, one eye	0.005	0.995	0.000
Z36.3 Antenatal screening for malformations using ultrasound and other physical methods	0.000	0.995	0.005
M19.14 Post-traumatic arthrosis of other joints (Hand)	0.005	0.995	0.000
Q66.3 Other congenital varus deformities of feet	0.005	0.995	0.000
C00 Malignant neoplasm of lip	0.005	0.995	0.000
Z36.1 Antenatal screening for raised alphafetoprotein level	0.000	0.995	0.005
M19.12 Post-traumatic arthrosis of other joints (Upper arm)	0.004	0.995	0.000
C10.9 Oropharynx, unspecified	0.004	0.995	0.000
M19.13 Post-traumatic arthrosis of other joints (Forearm)	0.004	0.996	0.000
Q66.7 Pes cavus	0.004	0.996	0.000
C13 Malignant neoplasm of hypopharynx	0.004	0.996	0.000
C11 Malignant neoplasm of nasopharynx	0.004	0.996	0.000
C03 Malignant neoplasm of gum	0.004	0.996	0.000
C83 Diffuse non-Hodgkin's lymphoma	0.000	0.996	0.004
C05.1 Soft palate	0.004	0.996	0.000
C04 Malignant neoplasm of floor of mouth	0.004	0.996	0.000
C06.8 Overlapping lesion of other and unspecified parts of mouth	0.004	0.996	0.000
C06.1 Vestibule of mouth	0.004	0.996	0.000
Q66.6 Other congenital valgus deformities of feet	0.004	0.996	0.000
C05.0 Hard palate	0.004	0.996	0.000
Q66.0 Talipes equinovarus	0.004	0.996	0.000
C14 Malignant neoplasm of other and ill-defined sites in the lip, oral cavity and pharynx	0.004	0.996	0.000
M19.19 Post-traumatic arthrosis of other joints (Site unspecified)	0.004	0.996	0.000
M19.18 Post-traumatic arthrosis of other joints (Other)	0.004	0.996	0.000
M19.16 Post-traumatic arthrosis of other joints-Lower leg	0.004	0.996	0.000
M19.15 Post-traumatic arthrosis of other joints (Pelvic region and thigh)	0.004	0.996	0.000
M19.10 Post-traumatic arthrosis of other joints (Multiple sites)	0.004	0.996	0.000
B97.8 Other viral agents as the cause of diseases classified to other chapters	0.004	0.996	0.000
X78.0 Home	0.004	0.996	0.000
C00.0 External upper lip	0.004	0.996	0.000
C01 Malignant neoplasm of base of tongue	0.004	0.996	0.000
C05.9 Palate, unspecified	0.004	0.996	0.000
C05.8 Overlapping lesion of palate	0.004	0.996	0.000
C05.2 Uvula	0.004	0.996	0.000
C10.8 Overlapping lesion of oropharynx	0.004	0.996	0.000
C10.4 Branchial cleft	0.004	0.996	0.000
C10.3 Posterior wall of oropharynx	0.004	0.996	0.000
C10.2 Lateral wall of oropharynx	0.004	0.996	0.000
C10.1 Anterior surface of epiglottis	0.004	0.996	0.000
C10.0 Vallecula	0.004	0.996	0.000
Q66.5 Congenital pes planus	0.004	0.996	0.000
Q66.4 Talipes calcaneovalgus	0.004	0.996	0.000
Q66.2 Metatarsus varus	0.004	0.996	0.000
Q66.1 Talipes calcaneovarus	0.004	0.996	0.000
Z36.5 Antenatal screening for isoimmunisation	0.000	0.996	0.004
C83.8 Other types of diffuse non-Hodgkin's lymphoma	0.000	0.996	0.004
Z36.4 Antenatal screening for foetal growth retardation using ultrasound and other physical methods	0.000	0.996	0.004
C08 Malignant neoplasm of other and unspecified major salivary glands	0.004	0.996	0.000
S02.40 Fracture of malar and maxillary bones (closed)	0.004	0.996	0.000
K76.7 Hepatorenal syndrome	0.004	0.996	0.000
K91.3 Postoperative intestinal obstruction	0.004	0.996	0.000
C07 Malignant neoplasm of parotid gland	0.004	0.996	0.000
C06.9 Mouth, unspecified	0.003	0.996	0.000
C09 Malignant neoplasm of tonsil	0.004	0.996	0.000
C00.9 Lip, unspecified	0.003	0.996	0.000
C00.8 Overlapping lesion of lip	0.003	0.996	0.000
C00.6 Commissure of lip	0.003	0.996	0.000
C00.5 Lip, unspecified, inner aspect	0.003	0.996	0.000
C00.4 Lower lip, inner aspect	0.003	0.996	0.000
C00.3 Upper lip, inner aspect	0.003	0.996	0.000
C00.2 External lip, unspecified	0.003	0.996	0.000
C00.1 External lower lip	0.003	0.996	0.000
C83.1 Small cleaved cell (diffuse)	0.000	0.996	0.004
J38.0 Paralysis of vocal cords and larynx	0.000	0.996	0.004
Q66.9 Congenital deformity of feet, unspecified	0.003	0.996	0.000
K75 Other inflammatory liver diseases	0.004	0.996	0.000
C83.7 Burkitt's tumour	0.000	0.996	0.003
Z35.5 Supervision of elderly primigravida	0.000	0.997	0.003
C03.9 Gum, unspecified	0.003	0.997	0.000
C03.1 Lower gum	0.003	0.997	0.000
C03.0 Upper gum	0.003	0.997	0.000
C11.8 Overlapping lesion of nasopharynx	0.003	0.997	0.000
C11.3 Anterior wall of nasopharynx	0.003	0.997	0.000
C11.2 Lateral wall of nasopharynx	0.003	0.997	0.000
C11.1 Posterior wall of nasopharynx	0.003	0.997	0.000
C11.0 Superior wall of nasopharynx	0.003	0.997	0.000
C13.9 Hypopharynx, unspecified	0.003	0.997	0.000
C13.8 Overlapping lesion of hypopharynx	0.003	0.997	0.000
C13.2 Posterior wall of hypopharynx	0.003	0.997	0.000
C13.1 Aryepiglottic fold, hypopharyngeal aspect	0.003	0.997	0.000
C13.0 Postcricoid region	0.003	0.997	0.000
C11.9 Nasopharynx, unspecified	0.003	0.997	0.000
C83.9 Diffuse non-Hodgkin's lymphoma, unspecified	0.000	0.997	0.003
Z94.7 Corneal transplant status	0.003	0.997	0.000
C83.6 Undifferentiated (diffuse)	0.000	0.997	0.003
C83.5 Lymphoblastic (diffuse)	0.000	0.997	0.003
C83.4 Immunoblastic (diffuse)	0.000	0.997	0.003
C83.2 Mixed small and large cell (diffuse)	0.000	0.997	0.003
C04.8 Overlapping lesion of floor of mouth	0.003	0.997	0.000
C04.1 Lateral floor of mouth	0.003	0.997	0.000
C04.0 Anterior floor of mouth	0.003	0.997	0.000
Z94.4 Liver transplant status	0.003	0.997	0.000
K76.6 Portal hypertension	0.003	0.997	0.000
C14.8 Overlapping lesion of lip, oral cavity and pharynx	0.003	0.997	0.000
C14.2 Waldeyer's ring	0.003	0.997	0.000
K75.3 Granulomatous hepatitis, not elsewhere classified	0.003	0.997	0.000
Z36.2 Other antenatal screening based on amniocentesis	0.000	0.997	0.003
C83.0 Small cell (diffuse)	0.000	0.997	0.003
I95.2 Hypotension due to drugs	0.000	0.997	0.003
C04.9 Floor of mouth, unspecified	0.003	0.997	0.000
C09.1 Tonsillar pillar (anterior) (posterior)	0.003	0.997	0.000
I61.5 Intracerebral haemorrhage, intraventricular	0.003	0.997	0.000
D89 Other disorders involving the immune mechanism, not elsewhere classified	0.000	0.997	0.003
H60.9 Otitis externa, unspecified	0.000	0.997	0.003
M19.11 Post-traumatic arthrosis of other joints (Shoulder region)	0.003	0.997	0.000
C08.8 Overlapping lesion of major salivary glands	0.003	0.997	0.000
C08.1 Sublingual gland	0.003	0.997	0.000
K70-K77 Diseases of liver	0.003	0.997	0.000
Q65.8 Other congenital deformities of hip	0.003	0.997	0.000
T83.8 Other complications of genito-urinary prosthetic devices, implants and grafts	0.000	0.997	0.003
C09.8 Overlapping lesion of tonsil	0.003	0.997	0.000
C09.0 Tonsillar fossa	0.003	0.997	0.000
C14.0 Pharynx, unspecified	0.003	0.997	0.000
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system	0.003	0.997	0.000
K72.1 Chronic hepatic failure	0.003	0.997	0.000
Q65 Congenital deformities of hip	0.003	0.997	0.000
K75.2 Nonspecific reactive hepatitis	0.003	0.997	0.000
K75.1 Phlebitis of portal vein	0.003	0.997	0.000
C08.0 Submandibular gland	0.003	0.997	0.000
K72 Hepatic failure, not elsewhere classified	0.003	0.997	0.000
Z94 Transplanted organ and tissue status	0.003	0.997	0.000
K75.0 Abscess of liver	0.003	0.997	0.000
K76 Other diseases of liver	0.003	0.997	0.000
D89.1 Cryoglobulinaemia	0.000	0.997	0.003
Z94.8 Other transplanted organ and tissue status	0.003	0.997	0.000
O03.4 Incomplete, without complication	0.003	0.997	0.000
N61 Inflammatory disorders of breast	0.003	0.997	0.000
K71 Toxic liver disease	0.003	0.997	0.000
K72.0 Acute and subacute hepatic failure	0.003	0.997	0.000
N49.2 Inflammatory disorders of scrotum	0.003	0.997	0.000
Q76 Congenital malformations of spine and bony thorax	0.002	0.997	0.000
Q76.4 Other congenital malformations of spine, not associated with scoliosis	0.002	0.997	0.000
C08.9 Major salivary gland, unspecified	0.002	0.997	0.000
I61.1 Intracerebral haemorrhage in hemisphere, cortical	0.003	0.997	0.000
H54.7 Unspecified visual loss	0.002	0.998	0.000
K70.1 Alcoholic hepatitis	0.002	0.998	0.000
Z94.3 Heart and lungs transplant status	0.002	0.998	0.000
D89.8 Other specified disorders involving the immune mechanism, not elsewhere classified	0.000	0.998	0.002
D89.3 Immune reconstitution syndrome	0.000	0.998	0.002
D89.0 Polyclonal hypergammaglobulinaemia	0.000	0.998	0.002
B98.0 Helicobacter pylori [H.pylori] as the cause of diseases classified to other chapters	0.000	0.998	0.002
K70.2 Alcoholic fibrosis and sclerosis of liver	0.002	0.998	0.000
K76.1 Chronic passive congestion of liver	0.002	0.998	0.000
Y42.7 Androgens and anabolic congeners	0.000	0.998	0.002
K77 Liver disorders in diseases classified elsewhere	0.002	0.998	0.000
K74 Fibrosis and cirrhosis of liver	0.002	0.998	0.000
M25.71 Osteophyte (Shoulder region)	0.002	0.998	0.000
K74.5 Biliary cirrhosis, unspecified	0.002	0.998	0.000
Z94.2 Lung transplant status	0.002	0.998	0.000
Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine	0.002	0.998	0.000
Q75 Other congenital malformations of skull and face bones	0.002	0.998	0.000
Q73 Reduction defects of unspecified limb	0.002	0.998	0.000
Q72 Reduction defects of lower limb	0.002	0.998	0.000
Q71 Reduction defects of upper limb	0.002	0.998	0.000
Q70 Syndactyly	0.002	0.998	0.000
Q69 Polydactyly	0.002	0.998	0.000
Q68 Other congenital musculoskeletal deformities	0.002	0.998	0.000
D89.9 Disorder involving the immune mechanism, unspecified	0.000	0.998	0.002
Q65.9 Congenital deformity of hip, unspecified	0.002	0.998	0.000
Q65.6 Unstable hip	0.002	0.998	0.000
Q65.5 Congenital subluxation of hip, unspecified	0.002	0.998	0.000
Q65.4 Congenital subluxation of hip, bilateral	0.002	0.998	0.000
Q65.3 Congenital subluxation of hip, unilateral	0.002	0.998	0.000
Q65.2 Congenital dislocation of hip, unspecified	0.002	0.998	0.000
Q65.1 Congenital dislocation of hip, bilateral	0.002	0.998	0.000
Q65.0 Congenital dislocation of hip, unilateral	0.002	0.998	0.000
K71.0 Toxic liver disease with cholestasis	0.002	0.998	0.000
K70 Alcoholic liver disease	0.002	0.998	0.000
Z94.9 Transplanted organ and tissue status, unspecified	0.002	0.998	0.000
Z94.6 Bone transplant status	0.002	0.998	0.000
Z94.5 Skin transplant status	0.002	0.998	0.000
Q67 Congenital musculoskeletal deformities of head, face, spine and chest	0.002	0.998	0.000
K76.5 Hepatic veno-occlusive disease	0.002	0.998	0.000
K76.4 Peliosis hepatis	0.002	0.998	0.000
K76.3 Infarction of liver	0.002	0.998	0.000
K76.2 Central haemorrhagic necrosis of liver	0.002	0.998	0.000
Z92.4 Personal history of major surgery, not elsewhere classified	0.002	0.998	0.000
K73 Chronic hepatitis, not elsewhere classified	0.002	0.998	0.000
X78 Intentional self-harm by sharp object	0.002	0.998	0.000
K71.1 Toxic liver disease with hepatic necrosis	0.002	0.998	0.000
Q76.1 Klippel-Feil syndrome	0.002	0.998	0.000
Q98.4 Klinefelter's syndrome, unspecified	0.002	0.998	0.000
I61.0 Intracerebral haemorrhage in hemisphere, subcortical	0.002	0.998	0.000
J38.6 Stenosis of larynx	0.000	0.998	0.002
K71.9 Toxic liver disease, unspecified	0.002	0.998	0.000
K71.8 Toxic liver disease with other disorders of liver	0.002	0.998	0.000
K71.7 Toxic liver disease with fibrosis and cirrhosis of liver	0.002	0.998	0.000
K71.6 Toxic liver disease with hepatitis, not elsewhere classified	0.002	0.998	0.000
K71.5 Toxic liver disease with chronic active hepatitis	0.002	0.998	0.000
K71.4 Toxic liver disease with chronic lobular hepatitis	0.002	0.998	0.000
K71.3 Toxic liver disease with chronic persistent hepatitis	0.002	0.998	0.000
K71.2 Toxic liver disease with acute hepatitis	0.002	0.998	0.000
I61 Intracerebral haemorrhage	0.002	0.998	0.000
Q74 Other congenital malformations of limb(s)	0.002	0.998	0.000
Z94.1 Heart transplant status	0.002	0.998	0.000
K75.9 Inflammatory liver disease, unspecified	0.002	0.998	0.000
Q76.9 Congenital malformation of bony thorax, unspecified	0.002	0.998	0.000
Q76.8 Other congenital malformations of bony thorax	0.002	0.998	0.000
Q76.7 Congenital malformation of sternum	0.002	0.998	0.000
Q76.6 Other congenital malformations of ribs	0.002	0.998	0.000
Q76.5 Cervical rib	0.002	0.998	0.000
Q76.3 Congenital scoliosis due to congenital bony malformation	0.002	0.998	0.000
Q76.2 Congenital spondylolisthesis	0.002	0.998	0.000
K73.2 Chronic active hepatitis, not elsewhere classified	0.002	0.998	0.000
K70.4 Alcoholic hepatic failure	0.002	0.998	0.000
S50.9 Superficial injury of forearm, unspecified	0.002	0.998	0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.002	0.998	0.000
D14.1 Larynx	0.002	0.998	0.000
J38.2 Nodules of vocal cords	0.000	0.998	0.002
H54 Blindness and low vision	0.002	0.998	0.000
Q78 Other osteochondrodysplasias	0.002	0.998	0.000
Q39.6 Diverticulum of oesophagus	0.002	0.998	0.000
J38 Diseases of vocal cords and larynx, not elsewhere classified	0.000	0.998	0.002
N64.1 Fat necrosis of breast	0.002	0.998	0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.002	0.998	0.000
H54.6 Unqualified visual loss, one eye	0.002	0.998	0.000
K74.4 Secondary biliary cirrhosis	0.002	0.998	0.000
K74.2 Hepatic fibrosis with hepatic sclerosis	0.002	0.998	0.000
K74.1 Hepatic sclerosis	0.002	0.998	0.000
K75.4 Autoimmune hepatitis	0.002	0.998	0.000
K77.8 Liver disorders in other diseases classified elsewhere	0.002	0.998	0.000
K77.0 Liver disorders in infectious and parasitic diseases classified elsewhere	0.002	0.998	0.000
H72 Perforation of tympanic membrane	0.000	0.998	0.002
I83.1 Varicose veins of lower extremities with inflammation	0.002	0.998	0.000
Q68.8 Other specified congenital musculoskeletal deformities	0.002	0.998	0.000
Q68.5 Congenital bowing of long bones of leg, unspecified	0.002	0.998	0.000
Q68.4 Congenital bowing of tibia and fibula	0.002	0.998	0.000
Q68.3 Congenital bowing of femur	0.002	0.998	0.000
Q68.2 Congenital deformity of knee	0.002	0.998	0.000
Q68.1 Congenital deformity of hand	0.002	0.998	0.000
Q68.0 Congenital deformity of sternocleidomastoid muscle	0.002	0.998	0.000
Q69.9 Polydactyly, unspecified	0.002	0.998	0.000
Q69.2 Accessory toe(s)	0.002	0.998	0.000
Q69.1 Accessory thumb(s)	0.002	0.998	0.000
Q69.0 Accessory finger(s)	0.002	0.998	0.000
Q70.9 Syndactyly, unspecified	0.002	0.998	0.000
Q70.4 Polysyndactyly	0.002	0.998	0.000
Q70.3 Webbed toes	0.002	0.998	0.000
Q70.2 Fused toes	0.002	0.998	0.000
Q70.1 Webbed fingers	0.002	0.998	0.000
Q70.0 Fused fingers	0.002	0.998	0.000
Q71.9 Reduction defect of upper limb, unspecified	0.002	0.998	0.000
Q71.8 Other reduction defects of upper limb(s)	0.002	0.998	0.000
Q71.6 Lobster-claw hand	0.002	0.998	0.000
Q71.5 Longitudinal reduction defect of ulna	0.002	0.998	0.000
Q71.4 Longitudinal reduction defect of radius	0.002	0.998	0.000
Q71.3 Congenital absence of hand and finger(s)	0.002	0.998	0.000
Q71.2 Congenital absence of both forearm and hand	0.002	0.998	0.000
Q71.1 Congenital absence of upper arm and forearm with hand present	0.002	0.998	0.000
Q71.0 Congenital complete absence of upper limb(s)	0.002	0.998	0.000
Q72.9 Reduction defect of lower limb, unspecified	0.002	0.998	0.000
Q72.8 Other reduction defects of lower limb(s)	0.002	0.998	0.000
Q72.7 Split foot	0.002	0.998	0.000
Q72.6 Longitudinal reduction defect of fibula	0.002	0.998	0.000
Q72.5 Longitudinal reduction defect of tibia	0.002	0.998	0.000
Q72.4 Longitudinal reduction defect of femur	0.002	0.998	0.000
Q72.3 Congenital absence of foot and toe(s)	0.002	0.998	0.000
Q72.2 Congenital absence of both lower leg and foot	0.002	0.998	0.000
Q72.1 Congenital absence of thigh and lower leg with foot present	0.002	0.998	0.000
Q72.0 Congenital complete absence of lower limb(s)	0.002	0.998	0.000
Q73.8 Other reduction defects of unspecified limb(s)	0.002	0.998	0.000
Q73.1 Phocomelia, unspecified limb(s)	0.002	0.998	0.000
Q73.0 Congenital absence of unspecified limb(s)	0.002	0.998	0.000
Q75.9 Congenital malformation of skull and face bones, unspecified	0.002	0.998	0.000
Q75.8 Other specified congenital malformations of skull and face bones	0.002	0.998	0.000
Q75.5 Oculomandibular dysostosis	0.002	0.998	0.000
Q75.4 Mandibulofacial dysostosis	0.002	0.998	0.000
Q75.3 Macrocephaly	0.002	0.998	0.000
Q75.2 Hypertelorism	0.002	0.998	0.000
Q75.1 Craniofacial dysostosis	0.002	0.998	0.000
Q75.0 Craniosynostosis	0.002	0.998	0.000
Q77.9 Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified	0.002	0.998	0.000
Q77.8 Other osteochondrodysplasia with defects of growth of tubular bones and spine	0.002	0.998	0.000
Q77.7 Spondyloepiphyseal dysplasia	0.002	0.998	0.000
Q77.6 Chondroectodermal dysplasia	0.002	0.998	0.000
Q77.5 Diastrophic dysplasia	0.002	0.998	0.000
Q77.4 Achondroplasia	0.002	0.998	0.000
Q77.3 Chondrodysplasia punctata	0.002	0.998	0.000
Q77.2 Short rib syndrome	0.002	0.998	0.000
Q77.1 Thanatophoric short stature	0.002	0.998	0.000
Q77.0 Achondrogenesis	0.002	0.998	0.000
O03 Spontaneous abortion	0.002	0.998	0.000
J94.8 Other specified pleural conditions	0.000	0.998	0.002
M25.72 Osteophyte (Upper arm)	0.000	0.998	0.002
Q67.8 Other congenital deformities of chest	0.002	0.998	0.000
Q67.7 Pectus carinatum	0.002	0.998	0.000
Q67.6 Pectus excavatum	0.002	0.998	0.000
Q67.3 Plagiocephaly	0.002	0.998	0.000
Q67.2 Dolichocephaly	0.002	0.998	0.000
Q67.1 Compression facies	0.002	0.998	0.000
Q67.0 Facial asymmetry	0.002	0.998	0.000
Q96 Turner's syndrome	0.002	0.998	0.000
S82.81 Fractures of other parts of lower leg (open)	0.002	0.998	0.000
I61.8 Other intracerebral haemorrhage	0.002	0.998	0.000
I61.4 Intracerebral haemorrhage in cerebellum	0.002	0.998	0.000
K74.0 Hepatic fibrosis	0.002	0.998	0.000
Q67.5 Congenital deformity of spine	0.002	0.998	0.000
K73.1 Chronic lobular hepatitis, not elsewhere classified	0.002	0.998	0.000
K73.0 Chronic persistent hepatitis, not elsewhere classified	0.002	0.998	0.000
K76.9 Liver disease, unspecified	0.002	0.998	0.000
Q67.4 Other congenital deformities of skull, face and jaw	0.002	0.998	0.000
X78.9 Unspecified place	0.002	0.998	0.000
X78.8 Other specified place	0.002	0.998	0.000
X78.7 Farm	0.002	0.998	0.000
X78.6 Industrial and construction area	0.002	0.998	0.000
X78.5 Trade and service area	0.002	0.998	0.000
X78.4 Street and highway	0.002	0.998	0.000
X78.3 Sports and athletics area	0.002	0.998	0.000
X78.2 School, other institution and public administrative area	0.002	0.998	0.000
X78.1 Residential institution	0.002	0.998	0.000
Q39 Congenital malformations of oesophagus	0.002	0.998	0.000
Q99 Other chromosome abnormalities, not elsewhere classified	0.002	0.998	0.000
I61.2 Intracerebral haemorrhage in hemisphere, unspecified	0.002	0.998	0.000
K73.8 Other chronic hepatitis, not elsewhere classified	0.002	0.998	0.000
Q96.9 Turner's syndrome, unspecified	0.002	0.998	0.000
Q74.0 Other congenital malformations of upper limb(s), including shoulder girdle	0.002	0.998	0.000
K70.0 Alcoholic fatty liver	0.002	0.998	0.000
Q74.9 Unspecified congenital malformation of limb(s)	0.002	0.998	0.000
Q74.8 Other specified congenital malformations of limb(s)	0.002	0.998	0.000
Q74.3 Arthrogryposis multiplex congenita	0.002	0.998	0.000
I61.6 Intracerebral haemorrhage, multiple localised	0.002	0.998	0.000
J38.5 Laryngeal spasm	0.000	0.998	0.002
O03.9 Complete or unspecified, without complication	0.002	0.998	0.000
O03.6 Complete or unspecified, complicated by delayed or excessive haemorrhage	0.002	0.998	0.000
Q17.5 Prominent ear	0.002	0.998	0.000
Q90 Down's syndrome	0.002	0.998	0.000
K74.6 Other and unspecified cirrhosis of liver	0.002	0.998	0.000
Q79 Congenital malformations of musculoskeletal system, not elsewhere classified	0.001	0.998	0.000
J69.0 Pneumonitis due to food and vomit	0.000	0.998	0.002
L29.0 Pruritus ani	0.000	0.998	0.002
O02.0 Blighted ovum and nonhydatidiform mole	0.002	0.998	0.000
Q98.9 Sex chromosome abnormality, male phenotype, unspecified	0.002	0.998	0.000
Q98.8 Other specified sex chromosome abnormalities, male phenotype	0.002	0.998	0.000
Q98.7 Male with sex chromosome mosaicism	0.002	0.998	0.000
Q98.6 Male with structurally abnormal sex chromosome	0.002	0.998	0.000
Q98.5 Karyotype 47,XYY	0.002	0.998	0.000
Q98.3 Other male with 46,XX karyotype	0.002	0.998	0.000
Q98.2 Klinefelter's syndrome, male with 46,XX karyotype	0.002	0.998	0.000
Q98.1 Klinefelter's syndrome, male with more than two X chromosomes	0.002	0.998	0.000
Q98.0 Klinefelter's syndrome karyotype 47,XXY	0.002	0.998	0.000
Q99.8 Other specified chromosome abnormalities	0.002	0.998	0.000
H54.3 Unqualified visual loss, both eyes	0.002	0.998	0.000
Q78.9 Osteochondrodysplasia, unspecified	0.001	0.998	0.000
Q78.8 Other specified osteochondrodysplasias	0.001	0.998	0.000
Q78.6 Multiple congenital exostoses	0.001	0.998	0.000
Q78.5 Metaphyseal dysplasia	0.001	0.998	0.000
Q78.4 Enchondromatosis	0.001	0.998	0.000
Q78.3 Progressive diaphyseal dysplasia	0.001	0.998	0.000
Q78.2 Osteopetrosis	0.001	0.998	0.000
Q78.1 Polyostotic fibrous dysplasia	0.001	0.998	0.000
S02.4 Fracture of malar and maxillary bones	0.002	0.998	0.000
F60.3 Emotionally unstable personality disorder	0.002	0.998	0.000
Q74.1 Congenital malformation of knee	0.001	0.998	0.000
M00.96 Pyogenic arthritis, unspecified (Lower leg)	0.002	0.998	0.000
H54.1 Blindness, one eye, low vision, other eye	0.002	0.998	0.000
K11.5 Sialolithiasis	0.000	0.998	0.002
K11.1 Hypertrophy of salivary gland	0.000	0.998	0.002
Q39.4 Oesophageal web	0.002	0.998	0.000
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified	0.002	0.998	0.000
Q95 Balanced rearrangements and structural markers, not elsewhere classified	0.002	0.998	0.000
Q93 Monosomies and deletions from the autosomes, not elsewhere classified	0.002	0.998	0.000
Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified	0.002	0.998	0.000
Q91 Edwards' syndrome and Patau's syndrome	0.002	0.998	0.000
K72.9 Hepatic failure, unspecified	0.002	0.998	0.000
O03.8 Complete or unspecified, with other and unspecified complications	0.002	0.998	0.000
Q76.0 Spina bifida occulta	0.001	0.998	0.000
M00.94 Pyogenic arthritis, unspecified (Hand)	0.002	0.998	0.000
M54.46 Lumbago with sciatica (Lumbar region)	0.000	0.998	0.002
C09.9 Tonsil, unspecified	0.001	0.998	0.000
H33.3 Retinal breaks without detachment	0.000	0.998	0.002
O03.7 Complete or unspecified, complicated by embolism	0.002	0.998	0.000
O03.5 Complete or unspecified, complicated by genital tract and pelvic infection	0.002	0.998	0.000
O03.3 Incomplete, with other and unspecified complications	0.002	0.998	0.000
O03.2 Incomplete, complicated by embolism	0.002	0.998	0.000
O03.0 Incomplete, complicated by genital tract and pelvic infection	0.002	0.998	0.000
I61.3 Intracerebral haemorrhage in brain stem	0.002	0.998	0.000
J38.7 Other diseases of larynx	0.000	0.998	0.002
N83.3 Acquired atrophy of ovary and Fallopian tube	0.002	0.998	0.000
Q74.2 Other congenital malformations of lower limb(s), including pelvic girdle	0.001	0.998	0.000
H54.2 Low vision, both eyes	0.002	0.998	0.000
Q96.8 Other variants of Turner's syndrome	0.001	0.998	0.000
Q96.4 Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome	0.001	0.998	0.000
Q96.3 Mosaicism, 45,X/46,XX or XY	0.001	0.998	0.000
Q96.2 Karyotype 46,X with abnormal sex chromosome, except iso (Xq)	0.001	0.998	0.000
Q96.1 Karyotype 46,X iso (Xq)	0.001	0.998	0.000
Q96.0 Karyotype 45,X	0.001	0.998	0.000
Q38-Q45 Other congenital malformations of the digestive system	0.002	0.998	0.000
M41.99 Scoliosis, unspecified (Site unspecified)	0.000	0.998	0.002
H33.5 Other retinal detachments	0.000	0.998	0.002
H72.8 Other perforations of tympanic membrane	0.000	0.998	0.002
Q23.1 Congenital insufficiency of aortic valve	0.000	0.998	0.002
Q39.9 Congenital malformation of oesophagus, unspecified	0.001	0.998	0.000
Q39.8 Other congenital malformations of oesophagus	0.001	0.998	0.000
Q39.5 Congenital dilatation of oesophagus	0.001	0.998	0.000
Q39.3 Congenital stenosis and stricture of oesophagus	0.001	0.998	0.000
Q39.2 Congenital tracheooesophageal fistula without atresia	0.001	0.998	0.000
Q39.1 Atresia of oesophagus with tracheooesophageal fistula	0.001	0.998	0.000
Q39.0 Atresia of oesophagus without fistula	0.001	0.998	0.000
Q90.9 Down's syndrome, unspecified	0.001	0.998	0.000
Q17 Other congenital malformations of ear	0.002	0.998	0.000
X78.99 Intentional self-harm by sharp object: Unspecified place: During unspecified activity	0.001	0.998	0.000
H72.1 Attic perforation of tympanic membrane	0.000	0.998	0.001
K65.9 Peritonitis, unspecified	0.000	0.998	0.002
Q99.9 Chromosomal abnormality, unspecified	0.001	0.998	0.000
Q99.2 Fragile X chromosome	0.001	0.998	0.000
Q99.1 46,XX true hermaphrodite	0.001	0.998	0.000
Q99.0 Chimera 46,XX/46,XY	0.001	0.998	0.000
C85.1 B-cell lymphoma, unspecified	0.000	0.998	0.002
N88.8 Other specified noninflammatory disorders of cervix uteri	0.002	0.998	0.000
H72.2 Other marginal perforations of tympanic membrane	0.000	0.998	0.001
Q24.8 Other specified congenital malformations of heart	0.002	0.998	0.000
F29 Unspecified nonorganic psychosis	0.002	0.998	0.000
N83 Noninflammatory disorders of ovary, Fallopian tube and broad ligament	0.002	0.998	0.000
I70.00 Atherosclerosis of aorta (without gangrene)	0.000	0.998	0.002
M15.1 Heberden's nodes (with arthropathy)	0.002	0.998	0.000
Q90.2 Trisomy 21, translocation	0.001	0.998	0.000
Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)	0.001	0.998	0.000
Q90.0 Trisomy 21, meiotic nondisjunction	0.001	0.998	0.000
Y87.2 Sequelae of events of undetermined intent	0.002	0.998	0.000
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.002	0.998	0.000
M89.88 Other specified disorders of bone (Other)	0.002	0.998	0.000
K74.3 Primary biliary cirrhosis	0.002	0.998	0.000
Q28.3 Other malformations of cerebral vessels	0.001	0.998	0.000
Q79.9 Congenital malformation of musculoskeletal system, unspecified	0.001	0.998	0.000
Q79.5 Other congenital malformations of abdominal wall	0.001	0.998	0.000
Q79.4 Prune belly syndrome	0.001	0.998	0.000
Q79.3 Gastroschisis	0.001	0.998	0.000
Q79.2 Exomphalos	0.001	0.998	0.000
Q79.1 Other congenital malformations of diaphragm	0.001	0.998	0.000
Q79.0 Congenital diaphragmatic hernia	0.001	0.998	0.000
Q43.8 Other specified congenital malformations of intestine	0.001	0.998	0.000
S86.8 Injury of other muscles and tendons at lower leg level	0.002	0.998	0.000
Q43 Other congenital malformations of intestine	0.001	0.998	0.000
M79.57 Residual foreign body in soft tissue (Ankle and foot)	0.001	0.998	0.000
S02.41 Fracture of malar and maxillary bones (open)	0.001	0.998	0.000
Q78.0 Osteogenesis imperfecta	0.001	0.998	0.001
M54.49 Lumbago with sciatica (Site unspecified)	0.000	0.998	0.001
Q91.7 Patau's syndrome, unspecified	0.001	0.998	0.000
Q91.6 Trisomy 13, translocation	0.001	0.998	0.000
Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)	0.001	0.998	0.000
Q91.4 Trisomy 13, meiotic nondisjunction	0.001	0.998	0.000
Q91.3 Edwards' syndrome, unspecified	0.001	0.998	0.000
Q91.2 Trisomy 18, translocation	0.001	0.998	0.000
Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)	0.001	0.998	0.000
Q91.0 Trisomy 18, meiotic nondisjunction	0.001	0.998	0.000
Q92.9 Trisomy and partial trisomy of autosomes, unspecified	0.001	0.998	0.000
Q92.8 Other specified trisomies and partial trisomies of autosomes	0.001	0.998	0.000
Q92.7 Triploidy and polyploidy	0.001	0.998	0.000
Q92.6 Extra marker chromosomes	0.001	0.998	0.000
Q92.5 Duplications with other complex rearrangements	0.001	0.998	0.000
Q92.4 Duplications seen only at prometaphase	0.001	0.998	0.000
Q92.3 Minor partial trisomy	0.001	0.998	0.000
Q92.2 Major partial trisomy	0.001	0.998	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.

Variant-specific associations