Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs187115 0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs1219648 0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs965513 0.742 0.200 9 97793827 intron variant A/G;T snv 15
rs13042395 0.752 0.160 20 773867 intron variant C/T snv 5.9E-02 13
rs11886868 0.752 0.280 2 60493111 intron variant C/T snv 0.65 12
rs11225395 0.776 0.360 11 102725749 intron variant A/C;G snv 11
rs1143633 0.752 0.280 2 112832890 intron variant C/G;T snv 11
rs13293512 0.763 0.360 9 94167461 intron variant T/C snv 0.24 11
rs4671393 0.790 0.400 2 60493816 intron variant A/C;G snv 11
rs966423 0.776 0.200 2 217445617 intron variant C/G;T snv 11
rs1143643 0.790 0.320 2 112830725 intron variant C/T snv 0.29 10
rs3020449 0.807 0.200 14 64306674 intron variant A/G;T snv 10
rs2439302 0.776 0.200 8 32574851 intron variant G/C snv 0.54 9
rs290481 0.827 0.200 10 113164066 intron variant C/T snv 0.20 9
rs4784227 0.807 0.160 16 52565276 intron variant C/T snv 0.20 8
rs10053538 0.807 0.160 5 157110499 intron variant C/A;T snv 7
rs16893344 0.807 0.160 8 133194036 intron variant C/T snv 0.29 7
rs34214448 0.851 0.120 17 51154651 intron variant G/T snv 0.39 7
rs3790843 0.827 0.160 1 200041696 intron variant C/T snv 0.29 7
rs13140012 0.827 0.320 4 186544404 intron variant T/A snv 0.41 6