| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs387906725 | 0.882 | 0.160 | X | 134475189 | missense variant | G/A | snv | 3 | |||
| rs137852485 | 0.925 | 0.120 | X | 134475358 | missense variant | C/A | snv | 2 | |||
| rs137852489 | 0.925 | 0.160 | X | 134486471 | stop gained | C/A;T | snv | 2.4E-05 | 2 | ||
| rs137852494 | 0.925 | 0.160 | X | 134475197 | stop gained | C/G;T | snv | 2 | |||
| rs1556030169 | 0.925 | 0.160 | X | 134498683 | frameshift variant | -/T | delins | 2 | |||
| rs369065223 | 0.925 | 0.160 | X | 134486514 | stop gained | C/G;T | snv | 5.5E-06 | 2 | ||
| rs1228634091 | 1.000 | 0.120 | X | 134475225 | missense variant | A/G | snv | 1.1E-05 | 1 | ||
| rs137852477 | 1.000 | 0.120 | X | 134490199 | missense variant | T/G | snv | 1 | |||
| rs137852478 | 1.000 | 0.120 | X | 134475285 | missense variant | A/T | snv | 1 | |||
| rs137852479 | 1.000 | 0.120 | X | 134498677 | missense variant | A/G | snv | 1 | |||
| rs137852482 | 1.000 | 0.120 | X | 134486475 | missense variant | C/T | snv | 1 | |||
| rs137852484 | 1.000 | 0.120 | X | 134493586 | missense variant | G/T | snv | 1 | |||
| rs137852498 | 1.000 | 0.120 | X | 134498407 | missense variant | C/T | snv | 1 | |||
| rs137852499 | 1.000 | 0.120 | X | 134473377 | missense variant | G/A | snv | 1 | |||
| rs137852500 | 1.000 | 0.120 | X | 134475218 | missense variant | G/A | snv | 1 | |||
| rs137852501 | 1.000 | 0.120 | X | 134475278 | missense variant | C/G | snv | 1 | |||
| rs137852502 | 1.000 | 0.120 | X | 134475201 | missense variant | A/G | snv | 1 | |||
| rs137852504 | 1.000 | 0.120 | X | 134498657 | missense variant | C/G | snv | 1 | |||
| rs137852506 | 1.000 | 0.120 | X | 134475239 | missense variant | C/T | snv | 1 |