Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10203477 0.925 0.200 2 60877850 intron variant A/T snv 0.48 2
rs10754558 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs11123810 0.925 0.200 2 100142823 intron variant T/C snv 0.37 2
rs11217040 0.925 0.200 11 118809939 regulatory region variant C/A snv 0.19 2
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs13119723 0.807 0.280 4 122297158 intron variant A/G snv 0.10 8
rs1457092 0.790 0.320 19 17193427 intron variant C/A snv 0.44 8
rs16867384 0.925 0.200 2 181246479 intron variant T/C snv 0.19 2
rs17264332 0.925 0.200 6 137684378 intron variant A/G;T snv 2
rs1738074 0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 9
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs212400 0.925 0.200 6 159052542 non coding transcript exon variant A/G snv 0.64 2
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs35761398 0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs394581 0.882 0.240 6 159061489 non coding transcript exon variant C/T snv 0.68 3
rs4073285 0.925 0.200 1 2608357 intron variant C/T snv 0.40 2
rs424232 0.882 0.240 6 32240547 intergenic variant C/A;T snv 3
rs4821124 0.851 0.240 22 21625000 downstream gene variant T/C snv 0.19 4
rs62323881 0.925 0.200 4 122117140 regulatory region variant C/A;T snv 2