| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
| rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
| rs1057519711 | 0.882 | 0.240 | 4 | 54733168 | missense variant | T/A | snv | 5 | |||
| rs1060502564 | 4 | 54695731 | missense variant | C/T | snv | 4.0E-06 | 2.1E-05 | 1 |