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: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		9 0 3 0.14 0 0
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		10 0 3 0.14 0 0
CUI: C0029925
Disease: Ovarian Carcinoma
Ovarian Carcinoma 		2 2 2 0.13 2 6.5E-02
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial 		2 2 2 0.13 2 6.5E-02
CUI: C4048328
Disease: cervical cancer
cervical cancer 		3 0 2 0.12 0 0
CUI: C0025202
Disease: melanoma
melanoma 		13 0 3 0.12 0 0
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		7 0 2 1.0E-01 0 0
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		8 0 2 9.5E-02 0 0
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		11 24 2 8.3E-02 2 3.8E-02
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome 		1 0 1 6.7E-02 0 0
CUI: C0206692
Disease: Carcinoma, Lobular
Carcinoma, Lobular 		1 0 1 6.7E-02 0 0
CUI: C0206711
Disease: Pilomatrixoma
Pilomatrixoma 		1 6 1 6.7E-02 2 5.7E-02
CUI: C0265552
Disease: Congenital macrodactylia
Congenital macrodactylia 		1 2 1 6.7E-02 1 3.1E-02
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		1 0 1 6.7E-02 0 0
CUI: C0406709
Disease: Hay-Wells syndrome
Hay-Wells syndrome 		1 0 1 6.7E-02 0 0
CUI: C0746787
Disease: Cancer of Neck
Cancer of Neck 		1 0 1 6.7E-02 0 0
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
Cardio-facio-cutaneous syndrome 		1 0 1 6.7E-02 0 0
CUI: C1336076
Disease: Sporadic Breast Carcinoma
Sporadic Breast Carcinoma 		1 0 1 6.7E-02 0 0
CUI: C1708349
Disease: Hereditary Diffuse Gastric Cancer
Hereditary Diffuse Gastric Cancer 		1 0 1 6.7E-02 0 0
CUI: C1785148
Disease: RAPP-HODGKIN SYNDROME
RAPP-HODGKIN SYNDROME 		1 0 1 6.7E-02 0 0
CUI: C1836860
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP J
FANCONI ANEMIA, COMPLEMENTATION GROUP J 		1 0 1 6.7E-02 0 0
CUI: C1838457
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP D1
FANCONI ANEMIA, COMPLEMENTATION GROUP D1 		1 0 1 6.7E-02 0 0
CUI: C1851878
Disease: OROFACIAL CLEFT 8
OROFACIAL CLEFT 8 		1 0 1 6.7E-02 0 0
CUI: C1854442
Disease: SPLIT-HAND/FOOT MALFORMATION 4
SPLIT-HAND/FOOT MALFORMATION 4 		1 0 1 6.7E-02 0 0
CUI: C1858562
Disease: ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3 		1 0 1 6.7E-02 0 0