| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894396 | 0.672 | 0.400 | 13 | 20189511 | stop gained | C/T | snv | 5.8E-04 | 1.1E-04 | 28 | |
| rs111033260 | 0.790 | 0.200 | 10 | 54317414 | stop gained | G/A;T | snv | 2.2E-04; 4.0E-06 | 7 | ||
| rs121908073 | 0.925 | 0.120 | 9 | 72694578 | stop gained | C/T | snv | 5.6E-05 | 3 | ||
| rs1244688796 | 0.925 | 0.200 | 21 | 34449584 | stop gained | C/T | snv | 4.0E-06 | 3 | ||
| rs565224393 | 0.882 | 0.200 | 11 | 78469304 | stop gained | A/C;G;T | snv | 4.0E-06; 4.0E-06 | 3 | ||
| rs779124360 | 0.925 | 0.200 | 21 | 34449585 | stop gained | C/T | snv | 4.0E-06 | 3 | ||
| rs1283780488 | 0.925 | 0.200 | 11 | 78469304 | stop gained | -/T | delins | 2 | |||
| rs397517255 | 0.925 | 0.200 | 9 | 114424483 | stop gained | G/A | snv | 2 | |||
| rs80356593 | 0.925 | 0.120 | 2 | 26477210 | stop gained | G/A | snv | 1.7E-04 | 3.5E-05 | 2 | |
| rs144964568 | 1.000 | 0.120 | 1 | 34785465 | stop gained | C/T | snv | 2.0E-05 | 1.4E-05 | 1 | |
| rs371465450 | 1.000 | 0.120 | 12 | 80255183 | stop gained | C/T | snv | 4.5E-05 | 7.0E-05 | 1 | |
| rs71524353 | 1.000 | 0.120 | 4 | 6300948 | stop gained | G/A;T | snv | 1.2E-03 | 1 | ||
| rs757774496 | 1.000 | 0.120 | 12 | 80279038 | stop gained | C/A;T | snv | 3.4E-05 | 4.2E-05 | 1 | |
| rs772862268 | 1.000 | 0.120 | 13 | 20223159 | stop gained | G/A | snv | 1.2E-05 | 2.8E-05 | 1 | |
| rs72474224 | 0.708 | 0.440 | 13 | 20189473 | missense variant | C/A;T | snv | 7.7E-03 | 18 | ||
| rs28931593 | 0.776 | 0.200 | 13 | 20189358 | missense variant | C/T | snv | 7.0E-06 | 9 | ||
| rs35887622 | 0.790 | 0.200 | 13 | 20189481 | missense variant | A/C;G | snv | 8.7E-03 | 8 | ||
| rs2274084 | 0.882 | 0.240 | 13 | 20189503 | missense variant | C/T | snv | 5.4E-02 | 2.2E-02 | 6 | |
| rs121908354 | 0.882 | 0.240 | 10 | 71570884 | missense variant | C/T | snv | 4.0E-05 | 7.0E-06 | 4 | |
| rs121912557 | 0.882 | 0.120 | 6 | 75857198 | missense variant | G/A | snv | 4 | |||
| rs759504704 | 0.882 | 0.200 | 11 | 78436786 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 4 | ||
| rs121908144 | 0.882 | 0.240 | 1 | 54999221 | missense variant | T/C | snv | 2.0E-05 | 3 | ||
| rs199606180 | 0.882 | 0.200 | 11 | 77206120 | missense variant | C/T | snv | 1.2E-05 | 2.1E-05 | 3 | |
| rs202138002 | 0.882 | 0.120 | 12 | 132621535 | missense variant | G/A;C | snv | 1.8E-05 | 3 | ||
| rs2274083 | 0.925 | 0.200 | 13 | 20189241 | missense variant | T/C | snv | 1.5E-02 | 5.1E-03 | 3 |