rs770572030, LIPG

N. diseases: 5
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.
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.827 0.160 18 49581427 missense variant T/A;C snv 4.0E-06; 4.0E-06 0.060 0.833 6 2008 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.827 0.160 18 49581427 missense variant T/A;C snv 4.0E-06; 4.0E-06 0.030 1.000 3 2014 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.827 0.160 18 49581427 missense variant T/A;C snv 4.0E-06; 4.0E-06 0.030 1.000 3 2014 2019
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.827 0.160 18 49581427 missense variant T/A;C snv 4.0E-06; 4.0E-06 0.010 1.000 1 2007 2007
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.827 0.160 18 49581427 missense variant T/A;C snv 4.0E-06; 4.0E-06 0.010 1.000 1 2011 2011