| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs672601334 | 0.752 | 0.400 | 1 | 155904798 | missense variant | G/C | snv | 17 | |||
| rs483352822 | 0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv | 16 | |||
| rs730881014 | 0.776 | 0.360 | 1 | 155904494 | stop gained | A/C;G;T | snv | 15 | |||
| rs869025195 | 0.790 | 0.280 | 1 | 155904493 | missense variant | T/G | snv | 11 | |||
| rs869025191 | 0.827 | 0.160 | 1 | 155904739 | missense variant | C/A;G;T | snv | 9 | |||
| rs869312687 | 0.925 | 0.080 | 1 | 155910695 | missense variant | T/G | snv | 8 | |||
| rs1557962794 | 0.882 | 0.160 | 1 | 155910693 | missense variant | T/G | snv | 4 | |||
| rs672601335 | 0.882 | 0.160 | 1 | 155904456 | missense variant | C/G | snv | 3 | |||
| rs869025189 | 0.925 | 0.160 | 1 | 155910658 | missense variant | C/G | snv | 7.0E-06 | 2 | ||
| rs869025197 | 0.925 | 0.160 | 1 | 155904475 | missense variant | A/G | snv | 2 | |||
| rs869025194 | 0.882 | 0.280 | 1 | 155904496 | missense variant | A/C;G;T | snv | 2 | |||
| rs869025193 | 0.925 | 0.160 | 1 | 155904498 | missense variant | T/C | snv | 2 | |||
| rs869025196 | 1.000 | 0.160 | 1 | 155904489 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs869025190 | 1.000 | 0.160 | 1 | 155910462 | missense variant | C/A | snv | 1 | |||
| rs869025192 | 1.000 | 0.160 | 1 | 155904499 | missense variant | C/G | snv | 1 | |||
| rs1557960039 | 1.000 | 1 | 155904472 | missense variant | T/C | snv | 1 |