| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121912491 | 0.882 | 0.240 | 3 | 49131128 | missense variant | C/T | snv | 7.0E-06 | 4 | ||
| rs121912489 | 0.925 | 0.240 | 3 | 49126449 | stop gained | G/C | snv | 2 | |||
| rs121912492 | 0.925 | 0.240 | 3 | 49130815 | missense variant | A/G | snv | 2 | |||
| rs267607207 | 0.925 | 0.240 | 3 | 49123216 | missense variant | G/T | snv | 2.5E-04 | 2.7E-04 | 2 | |
| rs267607208 | 0.925 | 0.240 | 3 | 49123179 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
| rs1553776921 | 0.925 | 0.240 | 3 | 49122170 | frameshift variant | -/C | delins | 2 | |||
| rs121912488 | 1.000 | 0.240 | 3 | 49131129 | missense variant | G/A | snv | 1.2E-05 | 1 | ||
| rs121912490 | 1.000 | 0.240 | 3 | 49130334 | stop gained | A/T | snv | 1 | |||
| rs1560072794 | 1.000 | 0.240 | 3 | 49124795 | frameshift variant | C/- | delins | 1 | |||
| rs730880125 | 1.000 | 0.240 | 3 | 49124920 | stop gained | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs746230397 | 1.000 | 0.240 | 3 | 49132500 | missense variant | A/C;G | snv | 8.0E-06; 4.0E-06 | 1 | ||
| rs888830612 | 1.000 | 0.240 | 3 | 49124700 | splice donor variant | C/A;T | snv | 8.0E-06 | 1.4E-05 | 1 | |
| rs1560063136 | 1.000 | 0.240 | 3 | 49121434 | frameshift variant | -/T | delins | 1 |