Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35761398 0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs2501432 0.716 0.480 1 23875430 missense variant T/C;G snv 0.62 16
rs7731626 0.716 0.240 5 56148856 intron variant G/A snv 0.30 16
rs879761216 0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs1893592 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 12
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs2305764 0.776 0.360 19 17203024 non coding transcript exon variant G/A snv 0.52 0.50 10
rs1457092 0.790 0.320 19 17193427 intron variant C/A snv 0.44 8
rs1738074 0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 9
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs6651252 0.790 0.200 8 128554935 intron variant T/C snv 0.19 8
rs13119723 0.807 0.280 4 122297158 intron variant A/G snv 0.10 8
rs17849502 0.827 0.240 1 183563445 missense variant G/A;C;T snv 4.0E-06; 4.0E-06; 3.4E-02 5
rs9275141 0.827 0.240 6 32683340 intergenic variant T/G snv 0.50 6
rs9357152 0.827 0.240 6 32697183 regulatory region variant A/G snv 0.24 5
rs947474 0.827 0.440 10 6348488 intron variant G/A snv 0.79 5
rs11066188 0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06 7
rs4821124 0.851 0.240 22 21625000 downstream gene variant T/C snv 0.19 4
rs394581 0.882 0.240 6 159061489 non coding transcript exon variant C/T snv 0.68 3
rs424232 0.882 0.240 6 32240547 intergenic variant C/A;T snv 3
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 5
rs10203477 0.925 0.200 2 60877850 intron variant A/T snv 0.48 2
rs11123810 0.925 0.200 2 100142823 intron variant T/C snv 0.37 2