Disease: Coronary Artery Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10757283 0.827 0.120 9 22134173 intergenic variant C/A;T snv 0.45 6
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs10920501 0.827 0.120 1 190092815 downstream gene variant A/T snv 0.18 5
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs12567209 0.807 0.080 1 162066689 upstream gene variant G/A snv 8.6E-02 6
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 5
rs13144478 0.882 0.040 4 115275150 regulatory region variant A/T snv 5.5E-02 4
rs139401390 0.851 0.120 10 88643382 regulatory region variant A/G snv 1.0E-02 5
rs16847548 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 8
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
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 8
rs186696265 0.882 0.040 6 160690668 intergenic variant C/T snv 1.0E-02 6
rs1870634 0.851 0.080 10 43985363 downstream gene variant T/G snv 0.59 4
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 9
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 10
rs2870463 0.882 0.040 16 75216819 upstream gene variant G/A snv 0.14 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
rs383830 0.882 0.040 5 100613278 intergenic variant A/T snv 0.76 3
rs3869109 0.851 0.160 6 31216419 intergenic variant A/G;T snv 5
rs3931020 0.882 0.040 1 74769633 downstream gene variant T/C snv 0.71 4