Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 35
rs121909231 0.667 0.600 10 87961095 stop gained C/A;T snv 29
rs121909219 0.689 0.400 10 87957915 stop gained C/A;T snv 24
rs863224909 0.732 0.360 10 87960952 stop gained C/A;G snv 14
rs121909232 0.776 0.160 10 87952258 stop gained C/A;G snv 4.0E-06 9
rs1114167640 0.790 0.160 10 87961067 stop gained TGACAAAGCAAATA/CGCTT delins 8
rs121909227 0.776 0.240 10 87957858 stop gained C/T snv 8
rs121909228 0.790 0.160 10 87957984 stop gained G/T snv 7
rs1554825165 0.790 0.160 10 87957872 stop gained C/A snv 7
rs397515374 0.790 0.160 10 87952159 stop gained TA/AT mnv 7
rs1085308048 0.851 0.320 10 87933175 stop gained T/G snv 4
rs1060500122 1.000 0.080 10 87933204 stop gained C/T snv 2
rs1554898053 1.000 0.080 10 87933018 stop gained C/T snv 2
rs587782607 1.000 0.080 10 87960914 stop gained G/A snv 2
rs786201816 1.000 0.080 10 87961100 stop gained C/G;T snv 4.0E-06 7.0E-06 2
rs786204929 0.752 0.200 10 87933144 stop gained G/A;T snv 2
rs1554898161 1.000 0.080 10 87933173 stop gained T/G snv 1
rs562015640 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 1
rs730882131 1.000 0.080 10 87957999 stop gained C/T snv 1
rs786204928 1.000 0.080 10 87933048 stop gained C/G;T snv 7.0E-06 1
rs869312778 1.000 0.080 10 87894063 stop gained G/T snv 1
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121909229 0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs121913293 0.732 0.360 10 87952142 missense variant C/A;T snv 18