| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs72653706 | 0.695 | 0.480 | 16 | 16163078 | stop gained | G/A | snv | 1.4E-03 | 1.2E-03 | 32 | |
| rs72657692 | 0.851 | 0.280 | 16 | 16169667 | missense variant | C/G;T | snv | 4.1E-06; 2.5E-05 | 10 | ||
| rs1564405163 | 0.807 | 0.280 | 10 | 8073746 | missense variant | G/C | snv | 6 | |||
| rs121909264 | 0.851 | 0.160 | 3 | 122257323 | missense variant | G/A | snv | 5 | |||
| rs750295789 | 0.925 | 0.040 | 11 | 13492788 | stop gained | G/T | snv | 4.0E-06 | 3 | ||
| rs1385228926 | 1.000 | 0.040 | 3 | 122284388 | missense variant | C/T | snv | 2 | |||
| rs104894165 | 0.925 | 0.240 | 10 | 8073747 | missense variant | A/G;T | snv | 4.0E-06 | 2 | ||
| rs104893959 | 0.925 | 0.040 | 6 | 10877343 | missense variant | C/A;T | snv | 2.0E-05; 8.0E-06 | 2 | ||
| rs104893960 | 0.925 | 0.040 | 6 | 10877296 | missense variant | C/T | snv | 4.0E-06 | 2.1E-05 | 2 | |
| rs759190203 | 1.000 | 0.040 | 6 | 10876442 | splice donor variant | -/A | delins | 4.0E-06 | 2 | ||
| rs780594439 | 0.925 | 0.040 | 6 | 10877155 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
| rs764623179 | 0.925 | 0.240 | 2 | 26284908 | missense variant | C/G;T | snv | 4.0E-06 | 2 | ||
| rs115230894 | 1.000 | 0.040 | 3 | 122282135 | missense variant | G/A;T | snv | 8.7E-04; 4.0E-06 | 1 | ||
| rs1246312399 | 1.000 | 0.040 | 2 | 26204107 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs1023807527 | 1.000 | 0.040 | 2 | 26284898 | missense variant | A/G | snv | 7.0E-06 | 1 |