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 GVH disease
CUI: C0856825
Disease: Acute GVH disease
49 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2012 2018
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 Hodgkin Lymphoma
CUI: C0220597
Disease: Adult Hodgkin Lymphoma
27 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2013 2018
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
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
176 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2014 2016
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.720 1.000 3 2012 2016
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
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.060 1.000 6 2007 2017
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
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.030 1.000 3 2009 2018
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