Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3761740
rs3761740
HMGCR
0.882 0.160 5 75336308 intron variant C/A snv 8.2E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2009 2009
dbSNP: rs3761740
rs3761740
HMGCR
0.882 0.160 5 75336308 intron variant C/A snv 8.2E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2013 2013
dbSNP: rs3761740
rs3761740
HMGCR
0.882 0.160 5 75336308 intron variant C/A snv 8.2E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.010 1.000 1 2010 2010
dbSNP: rs3761740
rs3761740
HMGCR
0.882 0.160 5 75336308 intron variant C/A snv 8.2E-02
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia 		0.010 1.000 1 2013 2013