rs1049673, 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.
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 0.010 1.000 1 2014 2014
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 0.010 1.000 1 2014 2014
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 0.010 1.000 1 2014 2014
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
81 0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 0.010 1.000 1 2012 2012
Intraocular pressure disorder
CUI: C0595921
Disease: Intraocular pressure disorder
56 0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 0.010 1.000 1 2018 2018
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 0.010 1.000 1 2010 2010
Multiple polyps
CUI: C0334108
Disease: Multiple polyps
32 0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 0.010 1.000 1 2018 2018