Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs995922697 0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs948562 11 58580292 intron variant A/G snv 0.15 1
rs9461776 0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02 11
rs9268853 0.790 0.440 6 32461866 intron variant T/C snv 0.29 10
rs879253942 0.677 0.400 17 7673826 missense variant A/G snv 28
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs869312777 0.925 0.120 10 87933245 missense variant C/G snv 3
rs867830180 0.925 0.120 20 63695147 missense variant G/A;T snv 3
rs867329357 0.925 0.120 13 102872275 missense variant G/A snv 4.0E-06 4.9E-05 3
rs867114783 17 7675109 missense variant T/C snv 6
rs8177400 0.882 0.160 11 126292695 missense variant G/A;C;T snv 2.8E-03; 1.2E-05 4
rs773919809 0.763 0.200 10 129766957 missense variant C/T snv 2.0E-05 13
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs751837 0.882 0.120 14 103018488 intron variant T/C snv 0.23 4
rs74790047 0.851 0.120 12 6601978 missense variant A/C;G snv 2.0E-05; 1.2E-04; 5.2E-03 1.7E-03 7
rs708486 0.925 0.120 14 52274253 intron variant A/G snv 0.35 3
rs707824 0.925 0.120 6 14636732 intergenic variant T/C snv 0.74 3
rs6773854 1.000 0.120 3 187931631 downstream gene variant T/C snv 0.23 2
rs6676671 0.882 0.160 1 206779403 intron variant T/A snv 0.32 4
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs63750250 0.807 0.280 7 5986933 frameshift variant -/T delins 1.6E-05 4.2E-05 9
rs61756766 0.776 0.320 22 41925447 missense variant G/A snv 5.7E-03 5.7E-03 9
rs61754966
NBN
0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 23
rs563378859 0.851 0.320 17 7675146 missense variant G/A snv 4.0E-06 2.1E-05 8
rs555607708 0.667 0.360 22 28695869 frameshift variant G/- del 2.0E-03 1.8E-03 33