Source: UNIPROT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs140593 | 0.925 | 0.160 | 15 | 48489896 | missense variant | C/G;T | snv | 1 | |||
| rs140599 | 0.925 | 0.160 | 15 | 48487317 | missense variant | C/T | snv | 1 | |||
| rs140603 | 0.925 | 0.160 | 15 | 48503845 | stop gained | G/A;C;T | snv | 7.6E-04 | 1 | ||
| rs141133182 | 1.000 | 0.160 | 15 | 48415735 | stop gained | C/A;T | snv | 2.1E-04 | 1 | ||
| rs363804 | 1.000 | 0.160 | 15 | 48441771 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs363815 | 1.000 | 0.160 | 15 | 48437370 | missense variant | A/G | snv | 1 | |||
| rs363853 | 1.000 | 0.160 | 15 | 48596292 | missense variant | A/G | snv | 1 | |||
| rs111401431 | 0.763 | 0.200 | 15 | 48468097 | missense variant | G/A | snv | 2 | |||
| rs137854464 | 0.851 | 0.200 | 15 | 48425483 | missense variant | C/T | snv | 7.0E-06 | 2 | ||
| rs137854480 | 0.742 | 0.200 | 15 | 48537629 | missense variant | G/A | snv | 2 | |||
| rs111984349 | 0.763 | 0.200 | 15 | 48415759 | missense variant | C/T | snv | 1 | |||
| rs137854475 | 0.882 | 0.200 | 15 | 48487155 | missense variant | C/T | snv | 1.3E-03 | 1.6E-03 | 1 | |
| rs25403 | 0.882 | 0.200 | 15 | 48613073 | missense variant | G/A | snv | 1 | |||
| rs137854461 | 0.790 | 0.280 | 15 | 48437026 | missense variant | T/C | snv | 1 | |||
| rs137854467 | 0.790 | 0.280 | 15 | 48600217 | missense variant | G/A | snv | 1 |