Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11676922 0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs221781 0.882 7 100698285 upstream gene variant A/G;T snv 4
rs17266594 0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 7
rs10516487 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs3733197 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs26232 0.925 0.160 5 103261019 intron variant C/T snv 0.30 4
rs391851 0.882 5 103342219 intergenic variant A/C;G;T snv 4
rs1320344 0.882 12 103493699 intron variant A/G snv 0.64 4
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs35018800 0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 9
rs55882956 19 10359243 missense variant G/A;C snv 7.2E-03; 4.1E-06 1
rs12720356 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs10444776 0.882 14 105647030 upstream gene variant G/A;T snv 4
rs1223438908 1.000 0.120 3 105681480 missense variant T/G snv 4.0E-06 2
rs752455542 1.000 0.120 3 105681740 missense variant T/G snv 4.0E-06 2
rs2305035 1.000 0.080 3 105720182 synonymous variant G/A snv 0.22 0.21 2
rs9657904 0.925 0.160 3 105867870 intron variant T/A;C snv 3
rs548234 0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs1921445 0.882 3 106229671 intergenic variant A/C;G snv 4
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14