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.
Abnormal behavior
CUI: C0233514
Disease: Abnormal behavior
121 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2019 2019
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
154 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2016 2016
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2017 2017
Cancer of Nasopharynx
CUI: C0238301
Disease: Cancer of Nasopharynx
12 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2014 2014
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2016 2016
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2016 2016
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2018 2018
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2014 2014
Childhood Renal Cell Carcinoma
CUI: C1333001
Disease: Childhood Renal Cell Carcinoma
10 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2014 2014
Cholangiocarcinoma
CUI: C0206698
Disease: Cholangiocarcinoma
43 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2019 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2019 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2019 2019
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2014 2014
Early gastric cancer
CUI: C0349530
Disease: Early gastric cancer
2 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2017 2017
Familial lichen amyloidosis
CUI: C0268398
Disease: Familial lichen amyloidosis
24 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2017 2017
Glaucoma, Primary Open Angle
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
222 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2019 2019
Glioma
CUI: C0017638
Disease: Glioma
353 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2018 2018
leukemia
CUI: C0023418
Disease: leukemia
144 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2018 2018
Malignant neoplasm of kidney
CUI: C0740457
Disease: Malignant neoplasm of kidney
22 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2014 2014
Malignant neoplasm of nasopharynx
CUI: C0153392
Disease: Malignant neoplasm of nasopharynx
10 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2014 2014
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2016 2016
Mental disorders
CUI: C0004936
Disease: Mental disorders
149 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1 2019 2019
Metabolic Diseases
CUI: C0025517
Disease: Metabolic Diseases
50 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2014 2014
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2016 2016
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
178 0.574 0.680 11 111511840 intron variant T/C snv 0.32 0.010 1.000 1 2014 2014