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.
Abnormal behavior
CUI: C0233514
Disease: Abnormal behavior
121 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2018 2018
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2012 2012
Acute pancreatitis
CUI: C0001339
Disease: Acute pancreatitis
51 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1 2013 2013
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2010 2010
Adolescent idiopathic scoliosis
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
1178 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2010 2010
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
Adult Liver Carcinoma
CUI: C0220630
Disease: Adult Liver Carcinoma
72 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2018 2018
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
Androgen-Insensitivity Syndrome
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
176 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1 2010 2010
Anthracosilicosis
CUI: C0003164
Disease: Anthracosilicosis
4 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2018 2018
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
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1 2018 2018
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
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2019 2019
Carcinoma, Basal Cell
CUI: C4721806
Disease: Carcinoma, Basal Cell
91 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2019 2019
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2019 2019
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
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2016 2016
Childhood asthma
CUI: C0264408
Disease: Childhood asthma
317 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2017 2017
Childhood Hodgkin Lymphoma
CUI: C0220644
Disease: Childhood Hodgkin Lymphoma
29 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2018 2018
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
CUI: C1302547
Disease: 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
Classical Hodgkin's Lymphoma
CUI: C1333064
Disease: Classical Hodgkin's Lymphoma
20 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2013 2013