rs200222843, APOB

N. diseases: 4
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 0.851 0.120 2 21003286 missense variant G/A snv 4.0E-05 4.2E-05 0.010 1.000 1 1989 1989
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.851 0.120 2 21003286 missense variant G/A snv 4.0E-05 4.2E-05 0.010 1.000 1 1989 1989
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
28 0.851 0.120 2 21003286 missense variant G/A snv 4.0E-05 4.2E-05 0.010 1.000 1 1989 1989
Hyperlipoproteinemia Type IIb
CUI: C1704417
Disease: Hyperlipoproteinemia Type IIb
16 0.851 0.120 2 21003286 missense variant G/A snv 4.0E-05 4.2E-05 0.010 1.000 1 1989 1989