rs2000813, LIPG

N. diseases: 9
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.
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
395 0.763 0.200 18 49567494 missense variant C/A;T snv 4.0E-06; 0.27; 4.0E-06 0.23 0.700 1.000 1 2012 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.763 0.200 18 49567494 missense variant C/A;T snv 4.0E-06; 0.27; 4.0E-06 0.23 0.030 0.667 3 2009 2015
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.763 0.200 18 49567494 missense variant C/A;T snv 4.0E-06; 0.27; 4.0E-06 0.23 0.020 1.000 2 2014 2016
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.763 0.200 18 49567494 missense variant C/A;T snv 4.0E-06; 0.27; 4.0E-06 0.23 0.010 1.000 1 2009 2009
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.763 0.200 18 49567494 missense variant C/A;T snv 4.0E-06; 0.27; 4.0E-06 0.23 0.010 1 2009 2009
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.763 0.200 18 49567494 missense variant C/A;T snv 4.0E-06; 0.27; 4.0E-06 0.23 0.010 1 2010 2010
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.763 0.200 18 49567494 missense variant C/A;T snv 4.0E-06; 0.27; 4.0E-06 0.23 0.010 1.000 1 2014 2014
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.763 0.200 18 49567494 missense variant C/A;T snv 4.0E-06; 0.27; 4.0E-06 0.23 0.010 1.000 1 2009 2009
Proliferative retinopathy
CUI: C0339467
Disease: Proliferative retinopathy
7 0.763 0.200 18 49567494 missense variant C/A;T snv 4.0E-06; 0.27; 4.0E-06 0.23 0.010 1.000 1 2014 2014