| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894972 | 0.807 | 0.240 | Y | 2787320 | missense variant | C/T | snv | 6 | |||
| rs121918655 | 0.851 | 0.200 | 9 | 124493143 | missense variant | C/T | snv | 5 | |||
| rs1217301314 | 0.827 | 0.240 | 11 | 57333494 | missense variant | T/C | snv | 1.2E-05 | 2.1E-05 | 5 | |
| rs201340156 | 0.882 | 0.200 | 9 | 124500571 | missense variant | G/A;C | snv | 6.7E-05 | 3 | ||
| rs104894966 | 0.882 | 0.200 | Y | 2787267 | missense variant | C/T | snv | 3 | |||
| rs104894971 | 0.882 | 0.200 | Y | 2787551 | missense variant | C/T | snv | 4.4E-05 | 3 |