Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1567542146 | 1.000 | 0.120 | 17 | 7670694 | frameshift variant | -/A | ins | 1 | |||
| rs1567549651 | 1.000 | 0.120 | 17 | 7674248 | frameshift variant | -/A | delins | 1 | |||
| rs1567550002 | 1.000 | 0.120 | 17 | 7674281 | frameshift variant | -/A | delins | 1 | |||
| rs1131691014 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 214 | |||
| rs1267047192 | 1.000 | 0.120 | 17 | 7675997 | frameshift variant | -/C | delins | 1 | |||
| rs1567551279 | 1.000 | 0.120 | 17 | 7674879 | frameshift variant | -/CACAC | delins | 1 | |||
| rs1195793509 | 1.000 | 0.120 | 17 | 7676210 | stop gained | -/CATT | delins | 1 | |||
| rs1567546889 | 1.000 | 0.120 | 17 | 7673711 | frameshift variant | -/CCCC | delins | 1 | |||
| rs1567556454 | 1.000 | 0.120 | 17 | 7676144 | frameshift variant | -/G | delins | 1 | |||
| rs1567553717 | 1.000 | 0.120 | 17 | 7675151 | inframe insertion | -/GGGCGGGGGTGTGGAATC | delins | 1 | |||
| rs1567548789 | 1.000 | 0.120 | 17 | 7674159 | coding sequence variant | -/GGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCATG | delins | 1 | |||
| rs1567551402 | 1.000 | 0.120 | 17 | 7674887 | frameshift variant | -/T | delins | 1 | |||
| rs1567556914 | 1.000 | 0.120 | 17 | 7676215 | frameshift variant | -/T | delins | 1 | |||
| rs1567548114 | 1.000 | 0.120 | 17 | 7673810 | frameshift variant | A/- | delins | 1 | |||
| rs1567550076 | 1.000 | 0.120 | 17 | 7674288 | frameshift variant | A/- | delins | 1 | |||
| rs1567552031 | 1.000 | 0.120 | 17 | 7674949 | frameshift variant | A/- | delins | 1 | |||
| rs1567554542 | 1.000 | 0.120 | 17 | 7675236 | frameshift variant | A/- | del | 1 | |||
| rs1567556114 | 1.000 | 0.120 | 17 | 7676091 | frameshift variant | A/- | del | 1 | |||
| rs1064793929 | 0.882 | 0.280 | 17 | 7675167 | frameshift variant | A/-;AA | delins | 5 | |||
| rs1555525279 | 1.000 | 0.120 | 17 | 7673795 | missense variant | A/C | snv | 2 | |||
| rs1567555667 | 1.000 | 0.120 | 17 | 7676031 | missense variant | A/C | snv | 1 | |||
| rs763746485 | 1.000 | 0.120 | 17 | 7674974 | splice region variant | A/C | snv | 1 | |||
| rs1057520002 | 0.695 | 0.360 | 17 | 7674242 | missense variant | A/C;G | snv | 20 | |||
| rs587781589 | 1.000 | 0.120 | 17 | 7674268 | missense variant | A/C;G | snv | 2 | |||
| rs1064796722 | 1.000 | 0.120 | 17 | 7676043 | missense variant | A/C;G | snv | 1 |