rs771676129, CD36

N. diseases: 7
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 0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 0.030 0.667 3 1999 2001
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 0.010 1 2012 2012
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 0.010 1.000 1 2007 2007
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 0.010 1 2007 2007
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 0.010 1.000 1 2007 2007
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 0.010 1.000 1 1999 1999
Retinal Diseases
CUI: C0035309
Disease: Retinal Diseases
56 0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 0.010 1.000 1 2003 2003