| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913500 | 0.529 | 0.600 | 2 | 208248388 | missense variant | C/A;G;T | snv | 4.0E-06 | 96 | ||
| rs1385943435 | 0.851 | 0.040 | 9 | 37002662 | missense variant | C/A;G;T | snv | 4.1E-06; 4.1E-06 | 5 | ||
| rs760031382 | 0.851 | 0.040 | 9 | 36966613 | missense variant | C/T | snv | 8.0E-06 | 5 |