rs12713559, APOB

N. diseases: 10
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.
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
123 0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 0.040 1.000 4 1997 2000
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
1423 0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 0.030 1.000 3 1997 2006
Hyperlipoproteinemia Type IIa
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
661 0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 0.030 1.000 3 1997 2006
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 0.010 1.000 1 1999 1999
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 0.010 1.000 1 1997 1997
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 0.010 1.000 1 1995 1995
Hyperlipoproteinemia Type IIb
CUI: C1704417
Disease: Hyperlipoproteinemia Type IIb
16 0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 0.010 1.000 1 1997 1997
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 0.010 1.000 1 1998 1998
Peripheral Vascular Diseases
CUI: C0085096
Disease: Peripheral Vascular Diseases
18 0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 0.010 1.000 1 1995 1995
Primary hypercholesterolemia
CUI: C0342879
Disease: Primary hypercholesterolemia
2 0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 0.010 1.000 1 1995 1995