| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs587777732 | 0.763 | 0.240 | 20 | 44406195 | missense variant | C/T | snv | 9 | |||
| rs113994205 | 0.827 | 0.160 | 17 | 3655305 | stop gained | G/A | snv | 4.8E-05 | 9.8E-05 | 5 | |
| rs780813696 | 0.827 | 0.240 | 20 | 44407388 | missense variant | C/A;T | snv | 4.1E-06 | 7.0E-06 | 5 | |
| rs121908125 | 0.882 | 0.160 | 17 | 3655304 | stop gained | G/A;C | snv | 8.0E-06 | 3 |