| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121909283 | 0.882 | 0.120 | 10 | 70435399 | stop gained | C/A;T | snv | 3.1E-04 | 4 | ||
| rs104894169 | 1.000 | 0.120 | 10 | 70435629 | missense variant | C/T | snv | 8.8E-05 | 2.2E-04 | 1 | |
| rs10999334 | 1.000 | 0.120 | 10 | 70435570 | missense variant | C/T | snv | 4.3E-04 | 1.6E-04 | 1 | |
| rs1310479365 | 1.000 | 0.120 | 10 | 70435327 | missense variant | C/A | snv | 7.0E-06 | 1 | ||
| rs1564667180 | 1.000 | 0.120 | 10 | 70435470 | frameshift variant | GGTGCCTC/- | delins | 1 | |||
| rs1564667617 | 1.000 | 0.120 | 10 | 70435984 | splice acceptor variant | C/A | snv | 1 | |||
| rs781366461 | 1.000 | 0.120 | 10 | 70435354 | missense variant | G/A | snv | 5.2E-05 | 1 | ||
| rs878855044 | 1.000 | 0.120 | 10 | 70435285 | splice donor variant | C/T | snv | 7.0E-06 | 1 |