| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894324 | 0.882 | 0.120 | 12 | 8606951 | missense variant | G/A | snv | 4.0E-06 | 3 | ||
| rs193922136 | 0.925 | 0.120 | X | 136659390 | missense variant | C/A;T | snv | 2 | |||
| rs104894768 | 1.000 | 0.120 | X | 136659309 | missense variant | G/T | snv | 1 | |||
| rs104894769 | 1.000 | 0.120 | X | 136659093 | missense variant | T/A;C | snv | 1 | |||
| rs104894771 | 1.000 | 0.120 | X | 136659332 | missense variant | G/C | snv | 1 | |||
| rs104894774 | 1.000 | 0.120 | X | 136648355 | missense variant | T/A;G | snv | 1 | |||
| rs104894775 | 1.000 | 0.120 | X | 136659048 | stop gained | G/A | snv | 1 | |||
| rs104894777 | 1.000 | 0.120 | X | 136659047 | missense variant | T/G | snv | 1 | |||
| rs104894778 | 1.000 | 0.120 | X | 136656377 | missense variant | C/A;T | snv | 5.5E-06 | 1 | ||
| rs1057521127 | 1.000 | 0.120 | X | 136659069 | missense variant | C/A | snv | 1 | |||
| rs1085307733 | 1.000 | 0.120 | X | 136659287 | stop gained | C/T | snv | 1 | |||
| rs1387503550 | 1.000 | 0.120 | X | 136659050 | missense variant | G/A;C | snv | 9.5E-06 | 1 | ||
| rs1477466218 | 1.000 | 0.120 | X | 136659399 | missense variant | G/A | snv | 5.5E-06 | 1 | ||
| rs148594123 | 1.000 | 0.120 | X | 136659284 | missense variant | G/A | snv | 1.1E-02 | 1.0E-02 | 1 | |
| rs1569376229 | 1.000 | 0.120 | X | 136650398 | splice donor variant | G/A | snv | 1 | |||
| rs1569376925 | 1.000 | 0.120 | X | 136654386 | frameshift variant | AAAGAGGAGAC/- | delins | 1 | |||
| rs1569376930 | 1.000 | 0.120 | X | 136654400 | frameshift variant | GAAA/- | delins | 1 | |||
| rs1569377829 | 1.000 | 0.120 | X | 136659261 | missense variant | C/A | snv | 1 | |||
| rs193922134 | 1.000 | 0.120 | X | 136650295 | frameshift variant | T/- | delins | 1 | |||
| rs193922135 | 1.000 | 0.120 | X | 136648279 | stop gained | C/T | snv | 1 | |||
| rs756468554 | 1.000 | 0.120 | X | 136659138 | missense variant | A/G | snv | 9.5E-06 | 1 | ||
| rs886039326 | 1.000 | 0.120 | X | 136659060 | missense variant | G/A | snv | 1 |