| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1060500053 | 1.000 | 0.120 | 17 | 70175721 | stop gained | C/T | snv | 4.0E-06 | 1 | ||
| rs1555603974 | 1.000 | 0.120 | 17 | 70175754 | stop gained | G/T | snv | 1 | |||
| rs199473369 | 1.000 | 0.120 | 17 | 70175250 | missense variant | G/A;C | snv | 1 | |||
| rs199473371 | 1.000 | 0.120 | 17 | 70175272 | missense variant | A/G | snv | 1 | |||
| rs199473380 | 1.000 | 0.120 | 17 | 70175500 | missense variant | G/T | snv | 1 | |||
| rs199473383 | 1.000 | 0.120 | 17 | 70175683 | missense variant | G/A | snv | 1 | |||
| rs199473650 | 1.000 | 0.120 | 17 | 70175200 | missense variant | G/T | snv | 1 | |||
| rs199473652 | 1.000 | 0.120 | 17 | 70175259 | missense variant | A/G | snv | 1 | |||
| rs199473655 | 1.000 | 0.120 | 17 | 70175614 | missense variant | C/T | snv | 1 | |||
| rs199473658 | 1.000 | 0.120 | 17 | 70175960 | missense variant | G/A | snv | 1 | |||
| rs797044841 | 1.000 | 0.120 | 17 | 70175306 | inframe deletion | GCTTTCGTCCTG/- | delins | 1 | |||
| rs797044842 | 1.000 | 0.120 | 17 | 70176005 | missense variant | G/C | snv | 1 | |||
| rs864622292 | 1.000 | 0.120 | 17 | 70175446 | missense variant | CCA/TTT | mnv | 1 |