Disease: Coronary Artery Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10106652 1.000 0.040 8 20070649 intergenic variant G/A snv 0.29 3
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 11
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 9
rs247616 1.000 0.040 16 56955678 intergenic variant C/T snv 0.29 8
rs2814944 1.000 0.040 6 34585020 downstream gene variant G/A snv 0.20 3
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 9
rs35237252 1.000 0.040 8 20012760 intergenic variant C/A;T snv 0.24 2
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 10
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 9
rs7136716 0.851 0.080 12 7538538 regulatory region variant A/G snv 0.22 6
rs7395662 0.882 0.080 11 48497341 downstream gene variant A/G snv 0.56 5
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 9
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs2472386
ABCA1
1.000 0.040 9 104839260 intron variant G/A snv 0.47 3
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 13
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17