| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13181 | 0.487 | 0.760 | 19 | 45351661 | stop gained | T/A;G | snv | 4.0E-06; 0.32 | 134 | ||
| rs1226085679 | 0.882 | 0.120 | 19 | 45351663 | missense variant | A/T | snv | 3 | |||
| rs1052559 | 1.000 | 0.040 | 19 | 45351661 | stop gained | T/A;G | snv | 2 | |||
| rs454421 | 1.000 | 0.040 | 19 | 45341392 | intron variant | C/G;T | snv | 0.44 | 1 |