Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61753219 0.672 0.400 6 42978330 missense variant G/A snv 3.6E-05 2.8E-05 64
rs1010184002 0.689 0.400 6 42978878 stop gained C/T snv 7.0E-06 60
rs779027563 0.677 0.360 17 42687838 missense variant G/C snv 4.0E-06 7.0E-06 58
rs780533096 0.701 0.600 13 23886338 missense variant C/G;T snv 4.8E-06; 9.6E-06 44
rs1555968941 0.752 0.280 12 2653847 missense variant G/A;C snv 31
rs34757931 0.742 0.360 11 119081189 missense variant T/G snv 1.2E-04 5.6E-05 26
rs387906799 0.742 0.200 2 240788118 missense variant G/A snv 19
rs886041091 0.807 0.120 9 84751990 missense variant A/G snv 18
rs2157719 0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 17
rs1555817157 0.742 0.280 20 25339320 frameshift variant TCTTCCTCAGGCG/- del 16
rs753611141 0.827 0.280 9 136418847 missense variant G/A;T snv 2.4E-05; 4.0E-06 14
rs672601370 0.790 0.160 2 240775863 missense variant G/A snv 13
rs768643552 0.851 0.240 9 136418630 missense variant G/A;C snv 4.0E-06 13
rs672601369 0.790 0.120 2 240783780 missense variant C/T snv 10
rs80356529 0.827 0.240 3 193643996 missense variant G/A;C snv 9
rs374997012 0.851 0.280 10 100989114 missense variant C/T snv 8.0E-06 7.0E-06 9
rs886037832 0.851 0.280 10 100988541 frameshift variant T/- delins 9
rs730882246 0.807 0.200 14 74494329 missense variant G/A snv 8
rs756421370 0.807 0.120 1 29200513 splice donor variant -/A delins 1.4E-04 6.3E-05 8
rs387906930 0.790 0.360 4 6301846 missense variant C/G;T snv 8
rs1057517686 0.827 0.120 1 1529299 missense variant C/T snv 7
rs672601367 0.851 0.080 2 240785066 missense variant T/G snv 7
rs74315205 0.807 0.360 4 6302385 missense variant G/A snv 7
rs1555303073 0.851 0.120 13 110176912 missense variant C/T snv 6
rs672601363 0.851 0.080 2 240788109 missense variant C/T snv 6