rs505151, PCSK9

N. diseases: 18
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.
Low density lipoprotein cholesterol measurement
1142 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 0.800 1.000 3 2012 2017
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 0.800 1.000 2 2012 2017
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 0.700 1.000 2 2012 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 0.050 1.000 5 2009 2020
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 0.040 0.750 4 2005 2015
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 0.040 0.750 4 2007 2015
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 0.020 1.000 2 2014 2015
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 0.010 1.000 1 2015 2015
Complicated malaria
CUI: C2747816
Disease: Complicated malaria
38 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 0.010 1.000 1 2018 2018
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 0.010 1.000 1 2020 2020
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 0.010 1.000 1 2020 2020
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
123 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 0.010 1.000 1 2015 2015
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
1423 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 0.010 1.000 1 2007 2007
Infarction, Lacunar
CUI: C0333559
Disease: Infarction, Lacunar
18 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 0.010 1 2017 2017
Malaria
CUI: C0024530
Disease: Malaria
148 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 0.010 1.000 1 2018 2018
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 0.010 1.000 1 2018 2018
Polygenic hypercholesterolemia
CUI: C0342880
Disease: Polygenic hypercholesterolemia
3 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 0.010 1.000 1 2006 2006
Vascular Diseases
CUI: C0042373
Disease: Vascular Diseases
40 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 0.010 1.000 1 2008 2008