| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs137853263 | 0.925 | 0.200 | X | 129562396 | missense variant | C/A;T | snv | 2 | |||
| rs776743373 | 0.925 | 0.200 | X | 129562373 | intron variant | G/A;T | snv | 2.2E-05 | 2 | ||
| rs1057515577 | 1.000 | 0.200 | X | 129553302 | intron variant | A/G | snv | 1 | |||
| rs1182741031 | 1.000 | 0.200 | X | 129575158 | stop gained | C/A;T | snv | 1 | |||
| rs137853260 | 1.000 | 0.200 | X | 129569296 | missense variant | G/A | snv | 1 | |||
| rs137853261 | 1.000 | 0.200 | X | 129569369 | missense variant | C/G | snv | 1 | |||
| rs137853828 | 1.000 | 0.200 | X | 129560552 | missense variant | T/C | snv | 1 | |||
| rs137853829 | 1.000 | 0.200 | X | 129560648 | missense variant | T/C | snv | 1 | |||
| rs137853830 | 1.000 | 0.200 | X | 129561184 | missense variant | A/G | snv | 1 | |||
| rs137853831 | 1.000 | 0.200 | X | 129562453 | missense variant | C/A;T | snv | 1.1E-05; 5.5E-06 | 1 | ||
| rs137853832 | 1.000 | 0.200 | X | 129562624 | missense variant | G/T | snv | 1 | |||
| rs137853834 | 1.000 | 0.200 | X | 129562657 | missense variant | T/G | snv | 1 | |||
| rs137853835 | 1.000 | 0.200 | X | 129562659 | missense variant | A/T | snv | 1 | |||
| rs137853836 | 1.000 | 0.200 | X | 129562663 | missense variant | C/T | snv | 1 | |||
| rs137853837 | 1.000 | 0.200 | X | 129562783 | missense variant | A/G | snv | 1 | |||
| rs137853838 | 1.000 | 0.200 | X | 129565878 | missense variant | G/A | snv | 1 | |||
| rs137853839 | 1.000 | 0.200 | X | 129567266 | missense variant | C/G | snv | 1 | |||
| rs137853840 | 1.000 | 0.200 | X | 129567299 | missense variant | G/A | snv | 1 | |||
| rs137853841 | 1.000 | 0.200 | X | 129567300 | missense variant | A/G | snv | 1 | |||
| rs137853842 | 1.000 | 0.200 | X | 129569292 | missense variant | G/C | snv | 1 | |||
| rs137853843 | 1.000 | 0.200 | X | 129569304 | missense variant | T/C | snv | 1 | |||
| rs137853844 | 1.000 | 0.200 | X | 129575956 | missense variant | C/A | snv | 1 | |||
| rs137853845 | 1.000 | 0.200 | X | 129590236 | missense variant | T/G | snv | 1 | |||
| rs137853847 | 1.000 | 0.200 | X | 129569335 | missense variant | A/G | snv | 1 | |||
| rs137853848 | 1.000 | 0.200 | X | 129562665 | missense variant | C/T | snv | 1 |