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
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.070 0.714 7 2009 2019
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.070 0.714 7 2009 2019
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.060 0.833 6 2010 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.040 1.000 4 2014 2019
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
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
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
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
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
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
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
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2019 2019
Experimental Organism Basal Cell Carcinoma
CUI: C3811653
Disease: Experimental Organism Basal Cell Carcinoma
63 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2019 2019
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2019 2019
Optic Neuritis
CUI: C0029134
Disease: Optic Neuritis
4 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2019 2019
Osteoarthritis, Knee
CUI: C0409959
Disease: Osteoarthritis, Knee
150 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2019 2019
Post-Traumatic Stress Disorder
CUI: C0038436
Disease: Post-Traumatic Stress Disorder
117 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1 2019 2019
Proliferative vitreoretinopathy
CUI: C0242852
Disease: Proliferative vitreoretinopathy
14 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2019 2019
Stomach Diseases
CUI: C0038354
Disease: Stomach Diseases
3 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2019 2019
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.070 1.000 7 2006 2018
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.040 1.000 4 2017 2018