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.
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
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
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
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1 2012 2012
Metabolic Diseases
CUI: C0025517
Disease: Metabolic Diseases
50 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1 2015 2015
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1 2016 2016
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
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
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
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
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
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.040 0.750 4 2007 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.040 0.750 4 2007 2018
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
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
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
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.060 1.000 6 2007 2017
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.050 1.000 5 2009 2017
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
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.040 1.000 4 2017 2018
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
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.040 1.000 4 2017 2018