rs3761740, HMGCR

N. diseases: 4
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.
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.882 0.160 5 75336308 intron variant C/A snv 8.2E-02 0.700 1.000 1 2009 2009
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.882 0.160 5 75336308 intron variant C/A snv 8.2E-02 0.010 1.000 1 2010 2010
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.882 0.160 5 75336308 intron variant C/A snv 8.2E-02 0.010 1.000 1 2013 2013
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
123 0.882 0.160 5 75336308 intron variant C/A snv 8.2E-02 0.010 1.000 1 2013 2013