Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 12
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 12
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 10
rs2069514 0.807 0.160 15 74745879 upstream gene variant G/A snv 0.13 9
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 9
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 8
rs4769793 0.807 0.120 13 29985289 intergenic variant G/C snv 8
rs36115365 0.807 0.160 5 1313127 upstream gene variant G/A;C;T snv 7
rs4105144 0.827 0.160 19 40852719 intron variant T/C snv 7
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 7
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs2736108 0.807 0.160 5 1297373 upstream gene variant C/T snv 0.24 6
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 6
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs12521436 0.827 0.120 5 143438042 upstream gene variant G/A snv 0.21 5
rs1454694 0.827 0.080 4 181276794 intergenic variant T/C snv 0.20 5
rs3130350 0.827 0.280 6 30360062 upstream gene variant G/T snv 7.1E-02 5
rs35755165 0.882 0.080 19 40840084 intron variant A/C;G snv 5
rs4912913 0.827 0.120 5 143438741 upstream gene variant T/C snv 0.48 5
rs9295740 0.827 0.120 6 27721723 intergenic variant G/A snv 0.27 5
rs10484399 0.851 0.240 6 27566749 intergenic variant A/G snv 5.4E-02 4