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.
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
Anthracosilicosis
CUI: C0003164
Disease: Anthracosilicosis
4 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2018 2018
High-Risk Neuroblastoma
CUI: C4725671
Disease: High-Risk Neuroblastoma
4 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2009 2009
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
African Burkitt's lymphoma
CUI: C0343640
Disease: African Burkitt's lymphoma
5 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2014 2014
Organ dysfunction syndrome
CUI: C0342953
Disease: Organ dysfunction syndrome
6 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2014 2014
Bacteremia
CUI: C0004610
Disease: Bacteremia
7 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Cerebral Thrombosis
CUI: C0079102
Disease: Cerebral Thrombosis
7 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Cerebral arterial thrombosis
CUI: C0795687
Disease: Cerebral arterial thrombosis
9 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Heart Failure, Diastolic
CUI: C1135196
Disease: Heart Failure, Diastolic
9 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2017 2017
Lesion of brain
CUI: C0221505
Disease: Lesion of brain
9 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2013 2013
Uveitis, Intermediate
CUI: C0042166
Disease: Uveitis, Intermediate
10 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Thrombosis of cerebral veins
CUI: C0151945
Disease: Thrombosis of cerebral veins
11 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
CUI: C1302547
Disease: Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
14 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
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
Tinnitus
CUI: C0040264
Disease: Tinnitus
14 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2016 2016
Urinary tract infection
CUI: C0042029
Disease: Urinary tract infection
14 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
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
Diabetic foot ulcer
CUI: C1456868
Disease: Diabetic foot ulcer
17 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2018 2018
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
Congenital arteriovenous malformation
CUI: C0003857
Disease: Congenital arteriovenous malformation
23 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2018 2018
Graft-vs-Host Disease
CUI: C0018133
Disease: Graft-vs-Host Disease
25 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2018 2018
Necrotizing enterocolitis in fetus OR newborn
CUI: C4082937
Disease: Necrotizing enterocolitis in fetus OR newborn
26 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
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
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
28 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2014 2014