| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1055285452 | 1.000 | 0.120 | 9 | 104793255 | missense variant | C/T | snv | 8.0E-06 | 1.4E-05 | 1 | |
| rs1322998567 | 1.000 | 0.120 | 9 | 104825707 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs137854494 | 1.000 | 0.120 | 9 | 104806276 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
| rs137854495 | 1.000 | 0.120 | 9 | 104822514 | missense variant | G/A | snv | 1.2E-05 | 1 | ||
| rs137854496 | 1.000 | 0.120 | 9 | 104831048 | missense variant | C/A;G | snv | 5.6E-05; 4.0E-05 | 1 | ||
| rs137854497 | 1.000 | 0.120 | 9 | 104804668 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs137854498 | 1.000 | 0.120 | 9 | 104798504 | missense variant | G/A;T | snv | 8.0E-06; 8.0E-06 | 1 | ||
| rs137854500 | 1.000 | 0.120 | 9 | 104814154 | missense variant | C/T | snv | 2.4E-05 | 1 | ||
| rs137854501 | 1.000 | 0.120 | 9 | 104786940 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs141021096 | 1.000 | 0.120 | 9 | 104819690 | missense variant | G/T | snv | 8.0E-06 | 1 | ||
| rs146292819 | 0.790 | 0.240 | 9 | 104794495 | missense variant | T/G | snv | 2.9E-04 | 3.8E-04 | 1 | |
| rs2853574 | 1.000 | 0.120 | 9 | 104831058 | missense variant | G/A | snv | 2.4E-05 | 4.3E-05 | 1 | |
| rs2853578 | 1.000 | 0.120 | 9 | 104831027 | missense variant | T/A;C | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs28937313 | 0.882 | 0.160 | 9 | 104822520 | missense variant | T/C | snv | 8.0E-06 | 1 | ||
| rs28937314 | 1.000 | 0.120 | 9 | 104822521 | missense variant | T/C;G | snv | 1 | |||
| rs564764153 | 1.000 | 0.120 | 9 | 104785453 | missense variant | C/G | snv | 1.5E-04 | 1.8E-04 | 1 | |
| rs745593394 | 1.000 | 0.120 | 9 | 104819625 | missense variant | G/A | snv | 1.2E-05 | 1.4E-05 | 1 | |
| rs758100110 | 0.925 | 0.120 | 9 | 104845527 | missense variant | C/T | snv | 4.0E-06 | 1 |