Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28937900 | 0.752 | 0.160 | 19 | 46756276 | missense variant | C/A;T | snv | 1.0E-03 | 37 | ||
| rs104894681 | 0.776 | 0.200 | 19 | 46756793 | missense variant | C/T | snv | 9.0E-06 | 10 | ||
| rs543163491 | 0.827 | 0.160 | 19 | 46755995 | missense variant | A/G;T | snv | 8.2E-05; 6.8E-06 | 6 | ||
| rs1554754182 | 0.827 | 0.200 | 9 | 105606576 | intron variant | G/T | snv | 5 | |||
| rs200198778 | 0.827 | 0.160 | 14 | 77278764 | missense variant | T/C | snv | 5.6E-05 | 9.8E-05 | 5 | |
| rs398124245 | 0.851 | 0.120 | 9 | 131523025 | frameshift variant | -/G | delins | 2.1E-04 | 4 | ||
| rs587777819 | 0.925 | 0.120 | 9 | 131523038 | frameshift variant | TC/-;TCTC | delins | 7.0E-06 | 3 | ||
| rs765230689 | 0.882 | 0.120 | 9 | 131512044 | stop gained | T/A;C | snv | 8.0E-06 | 3 | ||
| rs119463996 | 0.925 | 0.160 | 9 | 105604372 | missense variant | T/C | snv | 2 | |||
| rs150367385 | 0.925 | 0.120 | 9 | 131519447 | missense variant | C/G | snv | 1.6E-03 | 1.1E-03 | 2 | |
| rs119462981 | 1.000 | 0.120 | 9 | 131510401 | stop gained | C/T | snv | 7.0E-06 | 1 | ||
| rs1289335417 | 1.000 | 0.120 | 9 | 131507400 | missense variant | C/T | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs28941782 | 1.000 | 0.120 | 9 | 131506217 | missense variant | G/A | snv | 1 | |||
| rs587777817 | 1.000 | 0.120 | 9 | 131522970 | frameshift variant | -/G | delins | 1 | |||
| rs587777818 | 1.000 | 0.120 | 9 | 131515444 | inframe deletion | CCT/- | del | 1 | |||
| rs587777820 | 1.000 | 0.120 | 9 | 131507503 | inframe deletion | ATG/- | delins | 1 |