Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.810 1.000 2 2013 2018
dbSNP: rs1333049
rs1333049
0.614 0.520 9 22125504 intron variant G/C snv 0.41
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.900 0.944 2 2007 2019
dbSNP: rs2075650
rs2075650
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.710 1.000 1 2013 2017
dbSNP: rs1333048
rs1333048
0.683 0.320 9 22125348 intron variant A/C snv 0.44
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2007 2007
dbSNP: rs3217992
rs3217992
0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2014 2014
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.890 1.000 1 2007 2019
dbSNP: rs12190287
rs12190287
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.720 1.000 2 2013 2017
dbSNP: rs564398
rs564398
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.710 1.000 1 2007 2018
dbSNP: rs11556924
rs11556924
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.840 0.875 1 2013 2019
dbSNP: rs579459
rs579459
0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2014 2014
dbSNP: rs867186
rs867186
0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.810 1.000 1 2013 2018
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
0.720 1.000 1 2014 2016
dbSNP: rs501120
rs501120
0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.720 1.000 1 2011 2013
dbSNP: rs1746048
rs1746048
0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.740 1.000 1 2007 2019
dbSNP: rs7865618
rs7865618
0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2007 2007
dbSNP: rs12413409
rs12413409
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2014 2014
dbSNP: rs1333047
rs1333047
0.790 0.240 9 22124505 intron variant A/T snv 0.63
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2014 2014
dbSNP: rs1878406
rs1878406
0.807 0.200 4 147472512 intergenic variant C/A;G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.710 1.000 2 2013 2015
dbSNP: rs2954029
rs2954029
0.807 0.160 8 125478730 intron variant A/T snv 0.42
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.800 1.000 1 2013 2018
dbSNP: rs515135
rs515135
0.807 0.160 2 21063185 intergenic variant T/C snv 0.73
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.800 1.000 1 2013 2018
dbSNP: rs7049105
rs7049105
0.807 0.120 9 22028802 intron variant A/G snv 0.58
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2007 2007
dbSNP: rs974819
rs974819
0.807 0.080 11 103789839 intron variant T/A;C snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.820 1.000 1 2012 2018
dbSNP: rs9818870
rs9818870
0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.740 0.600 1 2011 2019
dbSNP: rs12526453
rs12526453
0.827 0.160 6 12927312 intron variant C/G snv 0.27
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.730 1.000 1 2013 2019
dbSNP: rs1333042
rs1333042
0.827 0.120 9 22103814 intron variant A/G snv 0.63
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.810 1.000 1 2007 2018