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.
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
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2015 2019
Cerebral Palsy
CUI: C0007789
Disease: Cerebral Palsy
69 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2011 2013
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
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 0.500 2 2018 2019
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: 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
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 0.500 2 2015 2019
Fatigue
CUI: C0015672
Disease: Fatigue
67 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2011 2012
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2012 2019
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
148 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 0.500 2 2013 2018
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2009 2012
Idiopathic scoliosis
CUI: C0595995
Disease: Idiopathic scoliosis
17 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2015 2016
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2016 2016
Intervertebral Disc Degeneration
CUI: C0158266
Disease: Intervertebral Disc Degeneration
47 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2011 2017
Irritable Bowel Syndrome
CUI: C0022104
Disease: Irritable Bowel Syndrome
52 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2017 2019
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
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2016 2018
Obesity
CUI: C0028754
Disease: Obesity
1111 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 0.500 2 2017 2019
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 0.500 2 2014 2019
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
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2017 2018
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
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