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: rs7136259
rs7136259
1.000 0.040 12 89687411 intron variant T/A;C;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.800 1.000 1 2012 2012
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs2681472
rs2681472
0.882 0.080 12 89615182 intron variant A/G snv 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs2681492
rs2681492
0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.700 1.000 1 2011 2011