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: C1335177
Disease: Ovarian Serous Adenocarcinoma
Ovarian Serous Adenocarcinoma 		23 0 5 0.10 0 0
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma 		41 0 5 7.5E-02 0 0
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		54 0 5 6.2E-02 0 0
CUI: C0278883
Disease: Metastatic melanoma
Metastatic melanoma 		54 0 5 6.2E-02 0 0
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		54 0 5 6.2E-02 0 0
CUI: C0345958
Disease: Large cell carcinoma of lung
Large cell carcinoma of lung 		32 0 3 5.0E-02 0 0
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		19 0 2 4.2E-02 0 0
CUI: C3165106
Disease: Infiltrating duct carcinoma of female breast
Infiltrating duct carcinoma of female breast 		21 0 2 4.0E-02 0 0
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme 		31 0 2 3.3E-02 0 0
CUI: C1334807
Disease: Mucinous carcinoma of breast
Mucinous carcinoma of breast 		1 0 1 3.2E-02 0 0
CUI: C1838244
Disease: TIBIAL MUSCULAR DYSTROPHY, TARDIVE
TIBIAL MUSCULAR DYSTROPHY, TARDIVE 		1 0 1 3.2E-02 0 0
CUI: C1840390
Disease: Pseudohypoaldosteronism, Type IIb
Pseudohypoaldosteronism, Type IIb 		1 0 1 3.2E-02 0 0
CUI: C1846862
Disease: PARKINSON DISEASE 8 (disorder)
PARKINSON DISEASE 8 (disorder) 		1 0 1 3.2E-02 0 0
CUI: C1858763
Disease: Cardiomyopathy, Dilated, 1g
Cardiomyopathy, Dilated, 1g 		1 0 1 3.2E-02 0 0
CUI: C1861065
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9 		1 0 1 3.2E-02 0 0
CUI: C1863599
Disease: Hereditary Myopathy with Early Respiratory Failure
Hereditary Myopathy with Early Respiratory Failure 		1 0 1 3.2E-02 0 0
CUI: C3151077
Disease: AORTIC ANEURYSM, FAMILIAL THORACIC 7
AORTIC ANEURYSM, FAMILIAL THORACIC 7 		1 0 1 3.2E-02 0 0
CUI: C4014814
Disease: MYOPATHY, CENTRONUCLEAR, 5
MYOPATHY, CENTRONUCLEAR, 5 		1 0 1 3.2E-02 0 0
CUI: C4225259
Disease: SMITH-KINGSMORE SYNDROME
SMITH-KINGSMORE SYNDROME 		1 0 1 3.2E-02 0 0
CUI: C4539997
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 108
DEAFNESS, AUTOSOMAL RECESSIVE 108 		1 0 1 3.2E-02 0 0
CUI: C4746575
Disease: ERYTHROLEUKEMIA, FAMILIAL, SUSCEPTIBILITY TO
ERYTHROLEUKEMIA, FAMILIAL, SUSCEPTIBILITY TO 		1 0 1 3.2E-02 0 0
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma 		3 0 1 3.0E-02 0 0
CUI: C1846385
Disease: FOCAL CORTICAL DYSPLASIA OF TAYLOR
FOCAL CORTICAL DYSPLASIA OF TAYLOR 		3 0 1 3.0E-02 0 0
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder 		4 0 1 2.9E-02 0 0
CUI: C0346163
Disease: Endometrioid carcinoma ovary
Endometrioid carcinoma ovary 		5 0 1 2.9E-02 0 0