| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs864321670 | 0.763 | 0.320 | 10 | 95633012 | missense variant | C/T | snv | 24 | |||
| rs863225045 | 0.790 | 0.360 | 10 | 95637327 | missense variant | C/A;T | snv | 15 | |||
| rs121434582 | 1.000 | 0.280 | 10 | 95643044 | missense variant | C/A;T | snv | 1.2E-05 | 1 | ||
| rs121434583 | 1.000 | 0.280 | 10 | 95606800 | missense variant | G/A | snv | 1 | |||
| rs1555262375 | 1.000 | 0.280 | 10 | 95633026 | frameshift variant | A/- | del | 1 | |||
| rs1555264243 | 1.000 | 0.280 | 10 | 95643118 | frameshift variant | C/- | del | 1 | |||
| rs2275272 | 1.000 | 0.280 | 10 | 95628405 | missense variant | G/A | snv | 0.11 | 0.10 | 1 | |
| rs537043237 | 1.000 | 0.280 | 10 | 95606856 | missense variant | C/T | snv | 1.2E-05 | 2.1E-05 | 1 | |
| rs587777858 | 1.000 | 0.280 | 10 | 95610272 | frameshift variant | G/- | delins | 1 | |||
| rs762742204 | 1.000 | 0.280 | 10 | 95621225 | missense variant | G/A | snv | 8.8E-05 | 1 | ||
| rs774047299 | 1.000 | 0.280 | 10 | 95606805 | missense variant | T/C;G | snv | 8.4E-05; 8.0E-06 | 1 | ||
| rs863223315 | 1.000 | 0.280 | 10 | 95613741 | splice donor variant | C/T | snv | 7.0E-06 | 1 |