Source: CURATED
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1060500909 | 0.925 | 0.120 | X | 103785717 | missense variant | T/C | snv | 2 | |||
| rs132630286 | 0.925 | 0.120 | X | 103788475 | missense variant | G/T | snv | 2 | |||
| rs398123467 | 0.925 | 0.120 | X | 103789373 | missense variant | G/C | snv | 2 | |||
| rs1060499653 | 1.000 | 0.120 | X | 103785752 | stop gained | G/T | snv | 1 | |||
| rs11543022 | 1.000 | 0.120 | X | 103785621 | missense variant | C/T | snv | 1 | |||
| rs132630280 | 1.000 | 0.120 | X | 103787811 | missense variant | C/G;T | snv | 1 | |||
| rs132630282 | 1.000 | 0.120 | X | 103787888 | missense variant | A/C | snv | 1 | |||
| rs132630283 | 1.000 | 0.120 | X | 103788485 | missense variant | T/C | snv | 1 | |||
| rs132630284 | 1.000 | 0.120 | X | 103787951 | missense variant | G/A;C | snv | 1 | |||
| rs132630285 | 1.000 | 0.120 | X | 103786493 | missense variant | G/A | snv | 1 | |||
| rs132630289 | 1.000 | 0.120 | X | 103785705 | missense variant | C/T | snv | 1 | |||
| rs132630296 | 1.000 | 0.120 | X | 103785746 | missense variant | G/T | snv | 1 | |||
| rs1569427311 | 1.000 | 0.120 | X | 103785743 | stop gained | C/T | snv | 1 | |||
| rs1569427707 | 1.000 | 0.120 | X | 103786730 | splice region variant | A/G | snv | 1 | |||
| rs1569428537 | 1.000 | 0.120 | X | 103789401 | splice region variant | G/T | snv | 1 | |||
| rs398123466 | 1.000 | 0.120 | X | 103788497 | missense variant | G/A | snv | 1 | |||
| rs886043504 | 1.000 | 0.120 | X | 103789375 | missense variant | G/A | snv | 1 | |||
| rs1064794255 | 1.000 | 0.120 | X | 103785675 | missense variant | G/A | snv | 1 | |||
| rs132630278 | 1.000 | 0.120 | X | 103788460 | missense variant | C/T | snv | 1 | |||
| rs132630279 | 1.000 | 0.120 | X | 103787831 | missense variant | T/C | snv | 1 | |||
| rs132630281 | 1.000 | 0.120 | X | 103788469 | missense variant | G/T | snv | 1 | |||
| rs132630293 | 0.925 | 0.120 | X | 103789361 | missense variant | C/T | snv | 1 | |||
| rs1556267215 | 1.000 | 0.120 | X | 103786657 | frameshift variant | CCAACATCAA/- | del | 1 | |||
| rs1556267388 | 1.000 | 0.120 | X | 103786728 | splice donor variant | T/C | snv | 1 | |||
| rs1556269487 | 1.000 | 0.120 | X | 103787961 | missense variant | T/G | snv | 1 |