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: rs1122608
rs1122608
0.763 0.120 19 11052925 intron variant G/T snv 0.18
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.720 1.000 3 2014 2016
dbSNP: rs55791371
rs55791371
0.925 0.080 19 11077477 intron variant A/C snv 0.11
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs56125973
rs56125973
1.000 0.040 19 11077488 intron variant T/C snv 0.13
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs56289821
rs56289821
1.000 0.040 19 11077571 intron variant G/A snv 0.10
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.700 1.000 1 2015 2015
dbSNP: rs11879293
rs11879293
0.882 0.120 19 10961934 intron variant G/A;C;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs12232780
rs12232780
0.807 0.080 19 11021404 non coding transcript exon variant G/A snv 0.23
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2017 2017