| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057519866 | 0.851 | 0.120 | 10 | 103093198 | missense variant | C/T | snv | 5 | |||
| rs11191580 | 0.827 | 0.040 | 10 | 103146454 | intron variant | T/C | snv | 7.9E-02 | 2 | ||
| rs72846714 | 1.000 | 0.120 | 10 | 103118697 | intron variant | G/A | snv | 0.15 | 1 | ||
| rs11598702 | 10 | 103138228 | intron variant | T/C;G | snv | 1 | |||||
| rs1424098571 | 1.000 | 0.040 | 10 | 103093263 | synonymous variant | G/A | snv | 4.0E-06 | 1 |