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.
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
328 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.040 1.000 4 2018 2020
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
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
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.030 1.000 3 2009 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.030 1.000 3 2007 2016
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.030 1.000 3 2008 2014
Depressive Symptoms
CUI: C0086132
Disease: Depressive Symptoms
120 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.030 1.000 3 2010 2016
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
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
386 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.030 1.000 3 2009 2018
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
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
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
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
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
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