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.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.882 0.200 1 156242034 intron variant T/C snv 0.20 0.010 1.000 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.882 0.200 1 156242034 intron variant T/C snv 0.20 0.010 1.000 1 2015 2015
Obesity
CUI: C0028754
Disease: Obesity
1111 0.882 0.200 1 156242034 intron variant T/C snv 0.20 0.010 1.000 1 2010 2010
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.882 0.200 1 156242034 intron variant T/C snv 0.20 0.010 1.000 1 2016 2016