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: rs170364
rs170364
1.000 0.040 16 57376022 intron variant T/G snv 0.74
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.020 1.000 2 2015 2015
dbSNP: rs614230
rs614230
1.000 0.040 16 57385374 downstream gene variant C/T snv 0.61
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2015 2015