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.
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
220 0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 0.700 1.000 1 2011 2011
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 0.020 1.000 2 2013 2014
Attention deficit hyperactivity disorder
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
420 0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 0.010 1.000 1 2012 2012
Cerebral Palsy
CUI: C0007789
Disease: Cerebral Palsy
69 0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 0.010 1.000 1 2011 2011
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 0.010 1.000 1 2019 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 0.010 1.000 1 2013 2013
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 0.010 1.000 1 2013 2013
Intellectual Disability
CUI: C3714756
Disease: Intellectual Disability
159 0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 0.010 1.000 1 2011 2011
Meningomyelocele
CUI: C0025312
Disease: Meningomyelocele
27 0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 0.010 1.000 1 2012 2012
Mental Retardation
CUI: C0025362
Disease: Mental Retardation
98 0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 0.010 1.000 1 2011 2011
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 0.010 1.000 1 2018 2018