| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs386834194 | 1.000 | 0.280 | 8 | 93808928 | missense variant | A/G | snv | 1.4E-05 | 1 | ||
| rs386834195 | 1.000 | 0.280 | 8 | 93808942 | stop gained | G/T | snv | 1 | |||
| rs386834196 | 1.000 | 0.280 | 8 | 93809057 | stop gained | A/T | snv | 1 | |||
| rs386834197 | 1.000 | 0.280 | 8 | 93809056 | frameshift variant | -/A | delins | 1 | |||
| rs386834198 | 1.000 | 0.280 | 8 | 93809811 | frameshift variant | -/TA | delins | 1 | |||
| rs386834199 | 1.000 | 0.280 | 8 | 93815437 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs386834200 | 1.000 | 0.280 | 8 | 93758552 | frameshift variant | AC/- | delins | 1 | |||
| rs386834201 | 1.000 | 0.280 | 8 | 93758557 | stop gained | T/A | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs386834203 | 1.000 | 0.280 | 8 | 93765574 | frameshift variant | A/- | del | 1 | |||
| rs386834204 | 1.000 | 0.280 | 8 | 93765642 | frameshift variant | A/- | delins | 1 | |||
| rs386834206 | 1.000 | 0.280 | 8 | 93780612 | missense variant | C/T | snv | 1 | |||
| rs386834207 | 1.000 | 0.280 | 8 | 93780872 | splice acceptor variant | A/G | snv | 1 | |||
| rs386834208 | 1.000 | 0.280 | 8 | 93780892 | missense variant | G/T | snv | 8.0E-06 | 1 | ||
| rs786205126 | 1.000 | 0.280 | 8 | 93809876 | inframe deletion | CTT/- | delins | 1 |