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: C1708349
Disease: Hereditary Diffuse Gastric Cancer
Hereditary Diffuse Gastric Cancer 		1 0 1 6.7E-02 0 0
CUI: C3150971
Disease: LEOPARD SYNDROME 3
LEOPARD SYNDROME 3 		1 0 1 6.7E-02 0 0
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		11 24 2 8.3E-02 2 3.8E-02
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial 		2 0 1 6.2E-02 0 0
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		579 375 6 1.0E-02 9 2.3E-02
CUI: C0740457
Disease: Malignant neoplasm of kidney
Malignant neoplasm of kidney 		2 2 1 6.2E-02 1 3.1E-02
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		7 0 2 1.0E-01 0 0
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas 		3 0 1 5.9E-02 0 0
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		5 0 1 5.3E-02 0 0
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
Malignant neoplasm of urinary bladder 		3 0 1 5.9E-02 0 0
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		2 0 1 6.2E-02 0 0
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		8 0 2 9.5E-02 0 0
CUI: C0025149
Disease: Medulloblastoma
Medulloblastoma 		2 0 1 6.2E-02 0 0
CUI: C1865285
Disease: Megalencephaly cutis marmorata telangiectatica congenita
Megalencephaly cutis marmorata telangiectatica congenita 		1 0 1 6.7E-02 0 0
CUI: C0025202
Disease: melanoma
melanoma 		13 0 3 0.12 0 0
CUI: C3554449
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 19
MENTAL RETARDATION, AUTOSOMAL DOMINANT 19 		1 0 1 6.7E-02 0 0
CUI: C0278883
Disease: Metastatic melanoma
Metastatic melanoma 		54 0 1 1.5E-02 0 0
CUI: C3150970
Disease: NOONAN SYNDROME 7
NOONAN SYNDROME 7 		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: C0029925
Disease: Ovarian Carcinoma
Ovarian Carcinoma 		2 2 2 0.13 2 6.5E-02
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome 		1 0 1 6.7E-02 0 0
CUI: C0206711
Disease: Pilomatrixoma
Pilomatrixoma 		1 6 1 6.7E-02 2 5.7E-02
CUI: C1785148
Disease: RAPP-HODGKIN SYNDROME
RAPP-HODGKIN SYNDROME 		1 0 1 6.7E-02 0 0
CUI: C0022603
Disease: Seborrheic keratosis
Seborrheic keratosis 		2 11 1 6.2E-02 1 2.4E-02
CUI: C1854442
Disease: SPLIT-HAND/FOOT MALFORMATION 4
SPLIT-HAND/FOOT MALFORMATION 4 		1 0 1 6.7E-02 0 0