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.
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.827 0.120 19 11113699 missense variant G/A snv 4.0E-06 0.010 1.000 1 2003 2003
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.827 0.120 19 11113699 missense variant G/A snv 4.0E-06 0.010 1.000 1 2003 2003
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.827 0.120 19 11113699 missense variant G/A snv 4.0E-06 0.010 1.000 1 2003 2003
Familial hypercholesterolemia - heterozygous
CUI: C0342882
Disease: Familial hypercholesterolemia - heterozygous
34 0.827 0.120 19 11113699 missense variant G/A snv 4.0E-06 0.010 1.000 1 2004 2004
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
1423 0.827 0.120 19 11113699 missense variant G/A snv 4.0E-06 0.010 1.000 1 2003 2003