Source: UNIPROT ×
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		460 370 36 3.6E-02 4 5.4E-03
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary 		15 31 6 1.0E-02 9 2.3E-02
CUI: C0025202
Disease: melanoma
melanoma 		13 0 4 6.8E-03 0 0
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		54 0 4 6.4E-03 0 0
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		7 0 3 5.1E-03 0 0
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma 		2 0 2 3.5E-03 0 0
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		2 0 2 3.5E-03 0 0
CUI: C0740457
Disease: Malignant neoplasm of kidney
Malignant neoplasm of kidney 		2 0 2 3.5E-03 0 0
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas 		3 1 2 3.4E-03 1 2.7E-03
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		19 0 2 3.4E-03 0 0
CUI: C1335177
Disease: Ovarian Serous Adenocarcinoma
Ovarian Serous Adenocarcinoma 		23 0 2 3.3E-03 0 0
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		26 0 2 3.3E-03 0 0
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme 		31 0 2 3.3E-03 0 0
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma 		41 0 2 3.2E-03 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		1 0 1 1.7E-03 0 0
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms 		1 0 1 1.7E-03 0 0
CUI: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne 		1 0 1 1.7E-03 0 0
CUI: C0017636
Disease: Glioblastoma
Glioblastoma 		1 0 1 1.7E-03 0 0
CUI: C0017920
Disease: Glycogen Storage Disease Type I
Glycogen Storage Disease Type I 		1 0 1 1.7E-03 0 0
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple 		1 0 1 1.7E-03 0 0
CUI: C0020071
Disease: Hereditary Sensory Autonomic Neuropathy, Type 1
Hereditary Sensory Autonomic Neuropathy, Type 1 		1 0 1 1.7E-03 0 0
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
Childhood Acute Lymphoblastic Leukemia 		1 0 1 1.7E-03 0 0
CUI: C0023601
Disease: Leydig Cell Tumor
Leydig Cell Tumor 		1 0 1 1.7E-03 0 0
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1 		1 0 1 1.7E-03 0 0
CUI: C0027832
Disease: Neurofibromatosis 2
Neurofibromatosis 2 		1 0 1 1.7E-03 0 0