| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894756 | 0.882 | 0.240 | X | 153905916 | missense variant | G/A;T | snv | 5.7E-06 | 3 | ||
| rs104894761 | 0.882 | 0.240 | X | 153905915 | missense variant | C/G;T | snv | 5.7E-06 | 3 | ||
| rs35095494 | 1.000 | 0.160 | 2 | 236581153 | missense variant | G/A;T | snv | 4.0E-03 | 1 | ||
| rs374029186 | 1.000 | 0.160 | 8 | 26756747 | 3 prime UTR variant | G/A | snv | 5.2E-05 | 3.5E-05 | 1 |