| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs281874674 | 0.827 | 0.280 | X | 108597479 | missense variant | G/C;T | snv | 8 | |||
| rs953686324 | 0.851 | 0.160 | 1 | 16044506 | frameshift variant | -/G | delins | 4.3E-06 | 5.6E-05 | 7 | |
| rs137853066 | 0.827 | 0.320 | 1 | 160042339 | missense variant | C/G;T | snv | 8.0E-06 | 7 | ||
| rs1553785033 | 0.882 | 0.120 | 3 | 170998321 | missense variant | C/T | snv | 6 | |||
| rs1419256494 | 0.882 | 0.280 | 19 | 7142938 | missense variant | A/G | snv | 4.0E-06 | 3 |