| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11571833 | 0.608 | 0.360 | 13 | 32398489 | stop gained | A/T | snv | 6.6E-03 | 6.0E-03 | 43 | |
| rs17107315 | 0.620 | 0.440 | 5 | 147828115 | missense variant | T/C | snv | 9.1E-03 | 8.2E-03 | 40 | |
| rs486907 | 0.667 | 0.360 | 1 | 182585422 | missense variant | C/T | snv | 0.31 | 0.28 | 32 | |
| rs74315364 | 0.732 | 0.200 | 1 | 182586014 | stop gained | C/A | snv | 3.6E-03; 4.0E-06 | 3.3E-03 | 13 | |
| rs63751127 | 0.882 | 0.200 | 2 | 47800177 | stop gained | C/A;T | snv | 4.0E-06; 4.0E-06 | 5 | ||
| rs1176026649 | 0.851 | 0.120 | 4 | 168921582 | missense variant | C/T | snv | 7.2E-06 | 4 | ||
| rs4503083 | 0.925 | 0.120 | 8 | 40015416 | stop gained | T/A | snv | 0.23 | 0.19 | 2 | |
| rs1187393388 | 1.000 | 0.120 | 2 | 47800567 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
| rs587779930 | 1.000 | 0.120 | 2 | 47801083 | missense variant | C/G;T | snv | 4.0E-06; 1.6E-05 | 1 |