| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121918346 | 0.882 | 0.040 | 3 | 16598169 | missense variant | T/C;G | snv | 8.0E-06 | 5 | ||
| rs41299088 | 1.000 | 0.040 | X | 133026798 | missense variant | G/A | snv | 2.6E-02 | 3.4E-02 | 2 | |
| rs61741870 | 1.000 | 0.040 | X | 133027727 | missense variant | A/G | snv | 2.6E-02 | 3.4E-02 | 2 | |
| rs769167142 | 1.000 | 0.040 | 9 | 128908798 | missense variant | G/A | snv | 1.6E-05 | 2.1E-05 | 1 | |
| rs781918360 | 1.000 | 0.040 | X | 102326266 | synonymous variant | C/T | snv | 2.8E-04 | 1 | ||
| rs1228406219 | 1.000 | 0.040 | 19 | 372700 | missense variant | G/A | snv | 1.6E-05 | 3.5E-05 | 1 |