| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1554074684 | 1.000 | 0.160 | 5 | 93585448 | missense variant | G/A;T | snv | 2 | |||
| rs1554074850 | 1.000 | 0.160 | 5 | 93588182 | stop gained | GC/CT | mnv | 1 | |||
| rs1554075105 | 1.000 | 0.160 | 5 | 93593685 | missense variant | T/C | snv | 1 | |||
| rs587777276 | 1.000 | 0.160 | 5 | 93588208 | missense variant | T/C | snv | 1 | |||
| rs1022192010 | 1.000 | 0.160 | 5 | 93585426 | missense variant | C/T | snv | 1 | |||
| rs863224903 | 1.000 | 0.160 | 5 | 93585405 | missense variant | T/C | snv | 1 | |||
| rs587777275 | 1.000 | 0.160 | 5 | 93585362 | missense variant | C/A;T | snv | 1 | |||
| rs1287146448 | 1.000 | 0.160 | 5 | 93585312 | missense variant | C/G;T | snv | 1 | |||
| rs587777274 | 1.000 | 0.160 | 5 | 93585367 | missense variant | G/C | snv | 1 | |||
| rs587777277 | 1.000 | 0.160 | 5 | 93585358 | missense variant | G/A | snv | 1 | |||
| rs1057519434 | 1.000 | 0.160 | 5 | 93585436 | missense variant | G/A | snv | 1 |