| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4072037 | 0.732 | 0.240 | 1 | 155192276 | splice acceptor variant | C/A;T | snv | 0.59 | 22 | ||
| rs1563221666 | 0.882 | 0.120 | 8 | 22162694 | missense variant | C/T | snv | 14 | |||
| rs121917834 | 0.790 | 0.080 | 8 | 22163096 | missense variant | T/A;C | snv | 3.6E-05 | 10 | ||
| rs80358263 | 0.827 | 0.280 | 14 | 74486378 | stop gained | G/T | snv | 8.4E-06 | 7 | ||
| rs879253740 | 0.882 | 0.240 | 14 | 74493191 | splice donor variant | A/G | snv | 5 | |||
| rs756021768 | 0.925 | 0.040 | 12 | 57512811 | missense variant | A/G;T | snv | 4.0E-06 | 2 | ||
| rs753455319 | 1.000 | 0.040 | Y | 1294330 | stop gained | C/A;T | snv | 1 |