Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11688000 1.000 0.040 2 75066030 intron variant A/G snv 0.34 1
rs10948172 0.882 0.040 6 44809954 intron variant A/G snv 0.27 3
rs2979715 1.000 0.040 8 79650024 intron variant C/T snv 0.77 1
rs2228314 0.790 0.360 22 41880738 missense variant G/C snv 0.34 0.38 8
rs1042667 1.000 0.040 17 72124410 3 prime UTR variant A/C snv 0.41 0.36 3
rs12601701 1.000 0.040 17 72119217 intron variant G/A snv 0.35 1
rs1566347 1.000 0.040 4 185811412 intron variant T/C snv 0.69 1
rs11177 0.851 0.080 3 52687289 missense variant G/A snv 0.38 0.33 4
rs12901071 0.882 0.160 15 67078051 intron variant A/G snv 0.25 3
rs12901499 0.882 0.040 15 67078107 intron variant G/A snv 0.45 3
rs2289263 0.925 0.120 15 67146869 intron variant T/G snv 0.43 3
rs6494629 0.925 0.120 15 67081773 intron variant C/T snv 0.52 2
rs12102171 1.000 0.040 15 67132695 intron variant C/T snv 0.22 1
rs12595334 1.000 0.040 15 67192818 3 prime UTR variant C/T snv 0.19 1
rs3743342 1.000 0.040 15 67193329 3 prime UTR variant C/T snv 0.20 1
rs8031440 1.000 0.040 15 67191641 3 prime UTR variant G/A snv 0.19 1
rs1560707 1.000 0.040 19 10640062 intron variant T/A;G snv 1
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs764256352 0.882 0.120 5 149981625 missense variant G/C snv 4.0E-06 2.1E-05 3
rs1052981 1.000 0.040 7 37906899 3 prime UTR variant G/A snv 0.70 1
rs1127379 0.882 0.120 8 41263761 3 prime UTR variant T/C snv 0.48 3
rs528981060 1.000 0.040 22 43266235 intron variant G/A snv 5.0E-04 1
rs62174901 1.000 0.040 2 165131833 intron variant T/C snv 0.12 1
rs62174906 1.000 0.040 2 165151847 intron variant A/G snv 0.13 1
rs6746030 0.763 0.320 2 166242648 missense variant A/G snv 0.88 0.88 16