| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs886039769 | 0.807 | 0.160 | 9 | 124500686 | missense variant | G/A | snv | 10 | |||
| rs104894119 | 0.807 | 0.160 | 9 | 124500685 | missense variant | C/T | snv | 7 | |||
| rs121918654 | 0.882 | 0.200 | 9 | 124503218 | missense variant | GC/TT | mnv | 6 | |||
| rs121918655 | 0.851 | 0.200 | 9 | 124493143 | missense variant | C/T | snv | 5 | |||
| rs1057517779 | 0.851 | 0.160 | 9 | 124493083 | missense variant | G/A | snv | 4 | |||
| rs104894124 | 0.925 | 0.160 | 9 | 124503353 | missense variant | C/T | snv | 2 | |||
| rs121918656 | 0.925 | 0.160 | 9 | 124503393 | start lost | C/T | snv | 2 | |||
| rs1564146922 | 0.925 | 0.160 | 9 | 124482917 | stop gained | G/C | snv | 2 | |||
| rs606231206 | 0.925 | 0.160 | 9 | 124500294 | frameshift variant | G/- | del | 2 | |||
| rs606231207 | 0.925 | 0.160 | 9 | 124500570 | frameshift variant | C/- | del | 2 | |||
| rs104894120 | 1.000 | 0.160 | 9 | 124482834 | missense variant | A/T | snv | 1 | |||
| rs104894123 | 1.000 | 0.160 | 9 | 124503348 | stop gained | G/A;T | snv | 8.1E-06 | 1 | ||
| rs104894125 | 1.000 | 0.160 | 9 | 124503089 | missense variant | C/T | snv | 1 | |||
| rs104894126 | 1.000 | 0.160 | 9 | 124500689 | missense variant | C/T | snv | 1 | |||
| rs1554721235 | 1.000 | 0.160 | 9 | 124493082 | missense variant | C/A;T | snv | 1 | |||
| rs1554721883 | 1.000 | 0.160 | 9 | 124503358 | frameshift variant | CACAG/ACAGGTCCAGGTC | delins | 1 | |||
| rs375469069 | 1.000 | 0.160 | 9 | 124500709 | missense variant | C/T | snv | 4.1E-06 | 1 | ||
| rs606231205 | 1.000 | 0.160 | 9 | 124503378 | frameshift variant | G/- | del | 1 | |||
| rs775441984 | 1.000 | 0.160 | 9 | 124503172 | stop gained | C/A;T | snv | 1 | |||
| rs863224904 | 1.000 | 0.160 | 9 | 124482934 | missense variant | A/C | snv | 1 |