rs1761667, CD36

N. diseases: 12
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.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.752 0.320 7 80615623 intron variant G/A snv 0.49 0.030 1.000 3 2015 2019
Obesity
CUI: C0028754
Disease: Obesity
1111 0.752 0.320 7 80615623 intron variant G/A snv 0.49 0.030 1.000 3 2015 2017
Adenomatous Polyposis Coli
CUI: C0032580
Disease: Adenomatous Polyposis Coli
237 0.752 0.320 7 80615623 intron variant G/A snv 0.49 0.010 1.000 1 2018 2018
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.752 0.320 7 80615623 intron variant G/A snv 0.49 0.010 1.000 1 2017 2017
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.752 0.320 7 80615623 intron variant G/A snv 0.49 0.010 1.000 1 2019 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.752 0.320 7 80615623 intron variant G/A snv 0.49 0.010 1.000 1 2019 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.752 0.320 7 80615623 intron variant G/A snv 0.49 0.010 1.000 1 2019 2019
FAMILIAL ADENOMATOUS POLYPOSIS, ATTENUATED (disorder)
7 0.752 0.320 7 80615623 intron variant G/A snv 0.49 0.010 1.000 1 2018 2018
Intraocular pressure disorder
CUI: C0595921
Disease: Intraocular pressure disorder
56 0.752 0.320 7 80615623 intron variant G/A snv 0.49 0.010 1.000 1 2018 2018
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.752 0.320 7 80615623 intron variant G/A snv 0.49 0.010 1.000 1 2012 2012
Multiple polyps
CUI: C0334108
Disease: Multiple polyps
32 0.752 0.320 7 80615623 intron variant G/A snv 0.49 0.010 1.000 1 2018 2018
Taste sweet
CUI: C0858600
Disease: Taste sweet
3 0.752 0.320 7 80615623 intron variant G/A snv 0.49 0.010 1.000 1 2018 2018