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 |