Source: ALL
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: C2676078
Disease: WHITE BLOOD CELL COUNT QUANTITATIVE TRAIT LOCUS 1
WHITE BLOOD CELL COUNT QUANTITATIVE TRAIT LOCUS 1 		2 1 2 0.13 1 6.2E-02
CUI: C3272797
Disease: Colon Serrated Polyposis
Colon Serrated Polyposis 		2 0 2 0.13 0 0
CUI: C4017326
Disease: DUFFY BLOOD GROUP SYSTEM, FY(a-b-) PHENOTYPE
DUFFY BLOOD GROUP SYSTEM, FY(a-b-) PHENOTYPE 		2 2 2 0.13 1 5.9E-02
CUI: C4017327
Disease: DUFFY BLOOD GROUP SYSTEM, FY(bwk) PHENOTYPE
DUFFY BLOOD GROUP SYSTEM, FY(bwk) PHENOTYPE 		2 0 2 0.13 0 0
CUI: C4310714
Disease: SESSILE SERRATED POLYPOSIS CANCER SYNDROME
SESSILE SERRATED POLYPOSIS CANCER SYNDROME 		2 0 2 0.13 0 0
CUI: C3150275
Disease: COMPLEMENT COMPONENT 2 DEFICIENCY
COMPLEMENT COMPONENT 2 DEFICIENCY 		11 0 3 0.13 0 0
CUI: C0268750
Disease: Necrotizing glomerulonephritis
Necrotizing glomerulonephritis 		3 0 2 0.12 0 0
CUI: C2697788
Disease: Interleukin 8 Measurement
Interleukin 8 Measurement 		5 0 2 0.11 0 0
CUI: C0038355
Disease: Stomach Diverticulum
Stomach Diverticulum 		1 0 1 6.7E-02 0 0
CUI: C0240709
Disease: Pericardial constriction
Pericardial constriction 		1 0 1 6.7E-02 0 0
CUI: C0266941
Disease: Derangement of temporomandibular joint
Derangement of temporomandibular joint 		1 0 1 6.7E-02 0 0
CUI: C0268288
Disease: Mild steroid 21-hydroxylase deficiency
Mild steroid 21-hydroxylase deficiency 		1 0 1 6.7E-02 0 0
CUI: C0272241
Disease: Complement abnormality
Complement abnormality 		1 0 1 6.7E-02 0 0
CUI: C0277526
Disease: Dysenteric diarrhea
Dysenteric diarrhea 		1 0 1 6.7E-02 0 0
CUI: C0343381
Disease: Verotoxigenic Escherichia coli gastrointestinal tract infection
Verotoxigenic Escherichia coli gastrointestinal tract infection 		1 0 1 6.7E-02 0 0
CUI: C0403411
Disease: Endocapillary glomerulonephritis
Endocapillary glomerulonephritis 		1 0 1 6.7E-02 0 0
CUI: C0523353
Disease: Complement factor H measurement
Complement factor H measurement 		1 0 1 6.7E-02 0 0
CUI: C0746351
Disease: Benign Lymphoproliferative Disorder
Benign Lymphoproliferative Disorder 		1 0 1 6.7E-02 0 0
CUI: C1268937
Disease: Diarrhea-negative hemolytic uremic syndrome
Diarrhea-negative hemolytic uremic syndrome 		1 0 1 6.7E-02 0 0
CUI: C1304408
Disease: Urticarial vasculitis
Urticarial vasculitis 		1 0 1 6.7E-02 0 0
CUI: C1444087
Disease: Disease due to Neisseria
Disease due to Neisseria 		1 0 1 6.7E-02 0 0
CUI: C1579873
Disease: Retinal thrombosis
Retinal thrombosis 		1 0 1 6.7E-02 0 0
CUI: C1853147
Disease: MACULAR DEGENERATION, AGE-RELATED, 4 (disorder)
MACULAR DEGENERATION, AGE-RELATED, 4 (disorder) 		1 0 1 6.7E-02 0 0
CUI: C1859995
Disease: Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency
Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency 		1 0 1 6.7E-02 0 0
CUI: C1859998
Disease: CARCINOMA, ADRENOCORTICAL, ANDROGEN-SECRETING
CARCINOMA, ADRENOCORTICAL, ANDROGEN-SECRETING 		1 0 1 6.7E-02 0 0