Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000113 0.925 0.040 5 150860514 intron variant C/T snv 0.13 1
rs1001007 0.827 0.120 3 46387167 intron variant A/G;T snv 5
rs10010325 1.000 0.040 4 105185196 intron variant C/A;G;T snv 3
rs1004234 0.827 0.120 5 132421409 intron variant A/G;T snv 5
rs1004819 0.776 0.360 1 67204530 intron variant G/A snv 0.30 1
rs10094579 0.807 0.280 8 89837077 downstream gene variant C/A snv 0.18 5
rs1016883 1.000 0.040 2 198016944 intron variant G/A snv 0.20 1
rs10174238 0.724 0.200 2 191108308 intron variant G/A snv 0.70 12
rs10185424 0.925 0.040 2 102046427 intron variant T/G snv 0.62 2
rs1047781 0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 2
rs1049526 0.925 0.040 6 32981027 3 prime UTR variant C/T snv 0.93 3
rs1050152 0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 1
rs10510607 0.827 0.120 3 28244770 intron variant C/T snv 0.15 5
rs1052571 0.882 0.080 1 15524118 missense variant G/A snv 0.50 0.59 1
rs10743181 0.827 0.120 11 2208529 regulatory region variant A/G snv 0.77 5
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs10750899 0.827 0.120 11 58517478 intergenic variant G/A snv 0.95 5
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 6
rs10761648 0.827 0.120 10 62594503 intron variant C/T snv 0.20 5
rs10761659 0.925 0.040 10 62685804 intron variant A/G snv 0.43 3
rs10775412 0.827 0.120 17 27542007 intron variant A/C snv 0.30 5
rs1077773 1.000 0.040 7 17403055 intron variant G/A;C snv 2
rs10781499 0.925 0.040 9 136371953 synonymous variant G/A snv 0.41 0.38 3
rs10797432 1.000 0.040 1 2569899 downstream gene variant C/T snv 0.51 2
rs10800309 0.925 0.120 1 161502368 upstream gene variant A/G;T snv 2