| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs118203945 | 0.882 | 0.280 | 1 | 11273836 | missense variant | A/G | snv | 3 | |||
| rs397514669 | 0.882 | 0.280 | 1 | 11285644 | missense variant | G/A | snv | 7.0E-06 | 3 | ||
| rs768272475 | 0.925 | 0.240 | 1 | 179345018 | synonymous variant | A/G | snv | 4.0E-06 | 2 | ||
| rs1057519051 | 0.882 | 0.200 | 5 | 132390825 | stop gained | T/G | snv | 3 | |||
| rs121908893 | 1.000 | 0.160 | 5 | 132385435 | stop gained | C/A;T | snv | 5.3E-04; 1.2E-04 | 3 | ||
| rs72552725 | 0.882 | 0.280 | 5 | 132370067 | missense variant | A/G | snv | 2.4E-05 | 2.1E-05 | 3 | |
| rs28383481 | 1.000 | 0.160 | 5 | 132393688 | missense variant | G/A | snv | 3.2E-03 | 3.4E-03 | 2 | |
| rs386134209 | 1.000 | 0.160 | 5 | 132387039 | frameshift variant | C/-;CC | delins | 7.0E-06 | 2 | ||
| rs1022453298 | 1.000 | 0.160 | 5 | 132370023 | frameshift variant | C/- | delins | 1 | |||
| rs1057516402 | 1.000 | 0.160 | 5 | 132394183 | splice acceptor variant | A/G | snv | 1 | |||
| rs1057516765 | 1.000 | 0.160 | 5 | 132378475 | stop gained | C/G | snv | 1 | |||
| rs1057516797 | 1.000 | 0.160 | 5 | 132370127 | frameshift variant | -/GACGCCG | delins | 1 | |||
| rs1057516805 | 1.000 | 0.160 | 5 | 132387024 | splice acceptor variant | G/C | snv | 1 | |||
| rs1057517069 | 1.000 | 0.160 | 5 | 132370366 | splice donor variant | G/A | snv | 1 | |||
| rs1057517106 | 1.000 | 0.160 | 5 | 132378377 | splice acceptor variant | G/T | snv | 1 | |||
| rs1057517306 | 1.000 | 0.160 | 5 | 132393678 | frameshift variant | -/C | delins | 1 | |||
| rs1057518297 | 1.000 | 0.160 | 5 | 132390889 | stop gained | C/T | snv | 1 | |||
| rs114269482 | 1.000 | 0.160 | 5 | 132385370 | missense variant | C/T | snv | 9.1E-05 | 1.8E-04 | 1 | |
| rs11568520 | 1.000 | 0.160 | 5 | 132370023 | missense variant | C/G | snv | 1.2E-04 | 4.9E-05 | 1 | |
| rs1157198543 | 1.000 | 0.160 | 5 | 132393745 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
| rs1178584184 | 1.000 | 0.160 | 5 | 132378412 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs121908886 | 1.000 | 0.160 | 5 | 132387044 | stop gained | C/T | snv | 4.0E-05 | 4.9E-05 | 1 | |
| rs121908887 | 1.000 | 0.160 | 5 | 132390838 | stop gained | -/A | delins | 1 | |||
| rs121908888 | 1.000 | 0.160 | 5 | 132384281 | missense variant | A/G | snv | 8.0E-06 | 7.0E-06 | 1 |