| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs72551307 | 0.925 | 0.080 | 2 | 168995403 | missense variant | T/C | snv | 1 | |||
| rs72549398 | 0.790 | 0.240 | 2 | 168932442 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs121908935 | 1.000 | 0.040 | 2 | 168976590 | missense variant | C/G | snv | 1 | |||
| rs756220860 | 1.000 | 0.040 | 2 | 168930693 | missense variant | C/T | snv | 4.2E-06 | 1.4E-05 | 1 | |
| rs72549400 | 1.000 | 0.040 | 2 | 168936268 | missense variant | C/G | snv | 1 | |||
| rs777469571 | 1.000 | 0.040 | 2 | 168936277 | missense variant | T/C;G | snv | 4.0E-06 | 1 | ||
| rs886043807 | 0.925 | 0.080 | 2 | 168970146 | missense variant | C/T | snv | 4.0E-06 | 2.8E-05 | 1 | |
| rs72549395 | 1.000 | 0.040 | 2 | 168927317 | missense variant | G/A;C | snv | 1.2E-05 | 1 | ||
| rs376216286 | 1.000 | 0.040 | 2 | 168964298 | missense variant | G/A;T | snv | 4.5E-05; 2.8E-05 | 1 | ||
| rs72549394 | 1.000 | 0.040 | 2 | 168923785 | missense variant | C/T | snv | 1 | |||
| rs72549402 | 0.925 | 0.080 | 2 | 168972040 | missense variant | T/C | snv | 2.0E-05 | 1.4E-05 | 1 | |
| rs369860506 | 1.000 | 0.040 | 2 | 168973734 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs72551306 | 1.000 | 0.040 | 2 | 168993781 | missense variant | C/A;G | snv | 1 | |||
| rs72549399 | 1.000 | 0.040 | 2 | 168935296 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs1274558905 | 1.000 | 0.040 | 2 | 168973768 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs72551305 | 1.000 | 0.040 | 2 | 168986187 | missense variant | A/T | snv | 1 |