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: rs2297508
rs2297508
0.790 0.240 17 17812003 synonymous variant C/G;T snv 0.50; 7.5E-05
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs9902941
rs9902941
1.000 0.040 17 17830446 intron variant C/T snv 0.56
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2017 2017