| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121918366 | 0.827 | 0.160 | 12 | 50992291 | missense variant | G/A;C | snv | 5 | |||
| rs121918367 | 0.827 | 0.080 | 12 | 50999214 | missense variant | C/A;T | snv | 6.0E-05 | 5 | ||
| rs121918365 | 0.882 | 0.080 | 12 | 50992810 | missense variant | C/G | snv | 1.4E-05 | 3 | ||
| rs137852311 | 0.882 | 0.120 | X | 55014830 | missense variant | G/A;T | snv | 3 |