| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121908641 | 0.882 | 0.120 | 9 | 130499545 | missense variant | G/A;T | snv | 3.2E-04; 4.0E-06 | 3 | ||
| rs121908646 | 0.925 | 0.120 | 9 | 130470873 | missense variant | T/C | snv | 8.7E-05 | 7.0E-05 | 2 | |
| rs201623252 | 0.925 | 0.120 | 9 | 130464127 | missense variant | G/A;T | snv | 4.0E-06 | 1.4E-05 | 2 | |
| rs121908647 | 0.925 | 0.120 | 9 | 130494981 | missense variant | G/T | snv | 2 | |||
| rs1004492719 | 1.000 | 0.120 | 9 | 130466762 | frameshift variant | TTCAAGGG/- | delins | 1 | |||
| rs1057516339 | 1.000 | 0.120 | 9 | 130464159 | stop gained | C/T | snv | 1 | |||
| rs1057516544 | 1.000 | 0.120 | 9 | 130464110 | splice region variant | G/- | delins | 1 | |||
| rs1057516648 | 1.000 | 0.120 | 9 | 130458451 | frameshift variant | G/- | delins | 1 | |||
| rs1057516960 | 1.000 | 0.120 | 9 | 130452231 | start lost | G/A | snv | 1 | |||
| rs1057517259 | 1.000 | 0.120 | 9 | 130471484 | splice acceptor variant | G/T | snv | 1 | |||
| rs1085307056 | 1.000 | 0.120 | 9 | 130479716 | missense variant | G/C | snv | 1 | |||
| rs1184442048 | 1.000 | 0.120 | 9 | 130466726 | missense variant | T/G | snv | 1 | |||
| rs121908636 | 1.000 | 0.120 | 9 | 130452268 | missense variant | G/A | snv | 2.8E-05 | 7.0E-06 | 1 | |
| rs121908637 | 1.000 | 0.120 | 9 | 130466774 | missense variant | G/A | snv | 8.0E-05 | 6.3E-05 | 1 | |
| rs121908638 | 1.000 | 0.120 | 9 | 130470877 | missense variant | G/A;T | snv | 4.0E-05; 4.0E-06 | 1 | ||
| rs121908639 | 1.000 | 0.120 | 9 | 130489464 | missense variant | G/A;T | snv | 3.6E-05; 4.0E-06 | 1 | ||
| rs121908642 | 1.000 | 0.120 | 9 | 130489404 | missense variant | C/T | snv | 3.2E-05 | 1.4E-05 | 1 | |
| rs121908643 | 1.000 | 0.120 | 9 | 130452281 | missense variant | C/T | snv | 1.2E-05 | 1.4E-05 | 1 | |
| rs121908644 | 1.000 | 0.120 | 9 | 130458482 | missense variant | C/T | snv | 4.4E-05 | 1.4E-05 | 1 | |
| rs121908645 | 1.000 | 0.120 | 9 | 130480446 | stop gained | C/T | snv | 2.4E-05 | 1.4E-05 | 1 | |
| rs121908648 | 1.000 | 0.120 | 9 | 130489422 | missense variant | A/C | snv | 8.0E-06 | 1 | ||
| rs1301613270 | 1.000 | 0.120 | 9 | 130489425 | stop gained | C/G;T | snv | 4.0E-06 | 1 | ||
| rs138279074 | 1.000 | 0.120 | 9 | 130458525 | missense variant | G/A | snv | 1.8E-04 | 1.8E-04 | 1 | |
| rs1396766124 | 1.000 | 0.120 | 9 | 130489465 | splice donor variant | G/A | snv | 4.0E-06 | 1 | ||
| rs148918985 | 1.000 | 0.120 | 9 | 130480404 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 |