Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2012 2014
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2012 2014
African Burkitt's lymphoma
CUI: C0343640
Disease: African Burkitt's lymphoma
5 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2014 2014
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2014 2014
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2014 2014
Fever
CUI: C0015967
Disease: Fever
66 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2014 2014
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
28 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2014 2014
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2014 2014
Organ dysfunction syndrome
CUI: C0342953
Disease: Organ dysfunction syndrome
6 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2014 2014
Complications of Diabetes Mellitus
CUI: C0342257
Disease: Complications of Diabetes Mellitus
35 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2009 2015
Diabetes Mellitus, Insulin-Dependent
954 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2009 2015
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2014 2015
Adult Diffuse Large B-Cell Lymphoma
CUI: C1332201
Disease: Adult Diffuse Large B-Cell Lymphoma
46 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Bacteremia
CUI: C0004610
Disease: Bacteremia
7 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Cerebral arterial thrombosis
CUI: C0795687
Disease: Cerebral arterial thrombosis
9 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Cerebral Thrombosis
CUI: C0079102
Disease: Cerebral Thrombosis
7 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
14 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
127 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Metabolic Diseases
CUI: C0025517
Disease: Metabolic Diseases
50 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1 2015 2015
Necrotizing enterocolitis in fetus OR newborn
26 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Pneumonia
CUI: C0032285
Disease: Pneumonia
33 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Sepsis
CUI: C0243026
Disease: Sepsis
144 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Septicemia
CUI: C0036690
Disease: Septicemia
141 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015