Disease: Coronary Artery Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 8
rs1867624 0.851 0.080 17 64309731 upstream gene variant C/T snv 0.65 4
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
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
rs2943650 0.827 0.120 2 226241205 intergenic variant C/T snv 0.58 6
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 9
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs7833904 0.882 0.040 8 58505103 upstream gene variant A/T snv 0.55 3
rs8042271 0.882 0.040 15 89030987 intergenic variant G/A;T snv 3
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 6
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs2066715
ABCA1
0.807 0.160 9 104825752 missense variant C/T snv 8.2E-02 5.5E-02 7
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs4149313
ABCA1
0.763 0.240 9 104824472 missense variant T/C snv 9
rs57137919
ABCG1 ; LOC105372814
0.776 0.160 21 42218908 intron variant G/A snv 0.14 9
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs3825807
ADAMTS7
0.807 0.120 15 78796769 missense variant A/G snv 0.34 0.33 10
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs185847354
ADIPOQ ; ADIPOQ-AS1
0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs6903956
ADTRP
0.763 0.160 6 11774350 intron variant A/G snv 0.65 10
rs2269422
AGER
0.882 0.040 6 32183517 intron variant T/C snv 1.7E-02 5.8E-03 3