Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2277680
rs2277680
0.776 0.160 17 4735268 missense variant G/A snv 0.47 0.41
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs3744700
rs3744700
0.882 0.080 17 4734715 intron variant T/G snv 0.66
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2015 2015