| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
| rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
| rs786202457 | 0.882 | 0.120 | 17 | 31350209 | stop gained | C/T | snv | 5 | |||
| rs797045139 | 0.882 | 0.120 | 17 | 31327718 | missense variant | C/A;G;T | snv | 4 | |||
| rs786202782 | 0.925 | 0.120 | 17 | 31223476 | frameshift variant | ACTA/- | delins | 3 |