Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs587783318 | 1.000 | 0.160 | 13 | 51935678 | missense variant | C/T | snv | 1.2E-04 | 4.2E-05 | 1 | |
| rs751202110 | 1.000 | 0.160 | 13 | 51958521 | stop gained | G/A;C;T | snv | 1.1E-04; 4.0E-06 | 1 | ||
| rs193922103 | 1.000 | 0.160 | 13 | 51958361 | missense variant | T/C | snv | 6.8E-05; 1.1E-04 | 1.5E-04 | 1 | |
| rs368589213 | 1.000 | 0.160 | 13 | 51950367 | missense variant | C/A;G;T | snv | 4.0E-06; 1.0E-04 | 1 | ||
| rs187046823 | 1.000 | 0.160 | 13 | 51968530 | missense variant | C/T | snv | 9.2E-05 | 1.4E-04 | 1 | |
| rs761147984 | 1.000 | 0.160 | 13 | 51944246 | missense variant | C/T | snv | 8.8E-05 | 2.8E-05 | 1 | |
| rs587783299 | 1.000 | 0.160 | 13 | 51961906 | missense variant | C/G | snv | 8.8E-05 | 6.3E-05 | 1 | |
| rs72552255 | 1.000 | 0.160 | 13 | 51946414 | missense variant | G/A | snv | 8.4E-05 | 1.2E-04 | 1 | |
| rs776280797 | 1.000 | 0.160 | 13 | 51939104 | missense variant | C/T | snv | 8.4E-05 | 5.6E-05 | 1 | |
| rs193922109 | 1.000 | 0.160 | 13 | 51937342 | stop gained | G/A | snv | 7.6E-05 | 8.4E-05 | 1 | |
| rs777879359 | 1.000 | 0.160 | 13 | 51941135 | missense variant | C/A;T | snv | 2.0E-05; 7.6E-05 | 1 | ||
| rs121907994 | 1.000 | 0.160 | 13 | 51950116 | missense variant | G/A | snv | 6.8E-05 | 1.4E-05 | 1 | |
| rs121907993 | 1.000 | 0.160 | 13 | 51949772 | missense variant | G/A;C;T | snv | 6.0E-05; 2.8E-05; 4.0E-06 | 1 | ||
| rs371840514 | 1.000 | 0.160 | 13 | 51946291 | missense variant | G/A;T | snv | 5.8E-05 | 1 | ||
| rs200728096 | 1.000 | 0.160 | 13 | 51961868 | missense variant | G/A | snv | 5.6E-05 | 1.0E-04 | 1 | |
| rs755554442 | 1.000 | 0.160 | 13 | 51941186 | missense variant | G/A;C | snv | 5.6E-05 | 3.5E-05 | 1 | |
| rs137853284 | 1.000 | 0.160 | 13 | 51958334 | missense variant | G/A;C | snv | 5.2E-05; 8.0E-06 | 1 | ||
| rs774102085 | 1.000 | 0.160 | 13 | 51974075 | missense variant | G/C | snv | 5.2E-05 | 5.6E-05 | 1 | |
| rs764131178 | 1.000 | 0.160 | 13 | 51944170 | missense variant | C/T | snv | 4.8E-05 | 1 | ||
| rs752850609 | 1.000 | 0.160 | 13 | 51964894 | missense variant | C/T | snv | 4.8E-05 | 1.4E-05 | 1 | |
| rs201497300 | 0.925 | 0.160 | 13 | 51946337 | missense variant | C/T | snv | 4.6E-05 | 2.8E-05 | 2 | |
| rs774028495 | 1.000 | 0.160 | 13 | 51946439 | missense variant | G/A | snv | 4.4E-05 | 7.0E-06 | 1 | |
| rs60431989 | 1.000 | 0.160 | 13 | 51941194 | missense variant | A/G | snv | 4.0E-05 | 3.5E-05 | 1 | |
| rs749085322 | 0.925 | 0.160 | 13 | 51941132 | missense variant | T/C | snv | 4.0E-05 | 2.1E-05 | 2 | |
| rs751078884 | 1.000 | 0.160 | 13 | 51946346 | missense variant | C/G;T | snv | 4.1E-06; 3.7E-05 | 1 |