| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs778768583 | 0.851 | 0.120 | 15 | 42410958 | missense variant | G/C | snv | 8.0E-06 | 10 | ||
| rs886042108 | 0.851 | 0.120 | 15 | 42409930 | splice acceptor variant | G/C;T | snv | 10 | |||
| rs143003434 | 1.000 | 0.080 | 2 | 32098840 | missense variant | G/A | snv | 3.2E-05 | 3.5E-05 | 7 | |
| rs886043676 | X | 31178766 | frameshift variant | G/- | del | 3 |