rs1866389, THBS4

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.
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.790 0.080 5 80065442 missense variant G/C snv 0.17 0.17 0.050 0.800 5 2002 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.790 0.080 5 80065442 missense variant G/C snv 0.17 0.17 0.030 0.667 3 2002 2015
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.790 0.080 5 80065442 missense variant G/C snv 0.17 0.17 0.010 1.000 1 2003 2003
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.790 0.080 5 80065442 missense variant G/C snv 0.17 0.17 0.010 1.000 1 2003 2003
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.790 0.080 5 80065442 missense variant G/C snv 0.17 0.17 0.010 1.000 1 2011 2011
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.790 0.080 5 80065442 missense variant G/C snv 0.17 0.17 0.010 1 2004 2004
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.790 0.080 5 80065442 missense variant G/C snv 0.17 0.17 0.010 1 2004 2004
Postinfarction
CUI: C0857175
Disease: Postinfarction
1 0.790 0.080 5 80065442 missense variant G/C snv 0.17 0.17 0.010 1.000 1 2011 2011
Premature coronary artery atherosclerosis
CUI: C1867743
Disease: Premature coronary artery atherosclerosis
43 0.790 0.080 5 80065442 missense variant G/C snv 0.17 0.17 0.010 1.000 1 2002 2002