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.
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
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
Osteoarthritis of hip
CUI: C0029410
Disease: Osteoarthritis of hip
121 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2010 2010
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.030 1.000 3 2011 2018
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
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
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
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2011 2011
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
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.030 1.000 3 2012 2018
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
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
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
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
Dementia, Vascular
CUI: C0011269
Disease: Dementia, Vascular
32 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2012 2012
Drug Resistant Epilepsy
CUI: C1096063
Disease: Drug Resistant Epilepsy
35 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2012 2012
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1 2012 2012
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2012 2012
Seizures
CUI: C0036572
Disease: Seizures
553 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2012 2012
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2012 2012
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
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
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
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