| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs763351020 | 0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 | 35 | ||
| rs138924661 | 0.807 | 0.120 | 17 | 56848773 | stop gained | G/A | snv | 9.1E-05 | 1.5E-04 | 9 | |
| rs35366573 | 0.882 | 0.120 | 1 | 207785101 | missense variant | C/T | snv | 1.5E-02 | 1.5E-02 | 3 | |
| rs121913060 | 0.925 | 0.120 | 1 | 196747131 | stop gained | G/T | snv | 1.2E-05 | 2 | ||
| rs760810105 | 1.000 | 0.120 | 8 | 27598502 | missense variant | G/T | snv | 4.0E-06 | 1 | ||
| rs1555599211 | 1.000 | 0.120 | 17 | 56848105 | intron variant | A/G | snv | 1 |