Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1156984408 | 1.000 | 15 | 48481682 | missense variant | C/T | snv | 4.0E-06 | 2.1E-05 | 1 | ||
| rs1555398830 | 1.000 | 15 | 48490037 | stop gained | C/A | snv | 1 | ||||
| rs1555401011 | 1.000 | 15 | 48526207 | missense variant | C/T | snv | 1 | ||||
| rs1566891701 | 1.000 | 15 | 48421675 | missense variant | A/G | snv | 1 | ||||
| rs1566892872 | 1.000 | 15 | 48425770 | stop gained | G/C | snv | 1 | ||||
| rs1566898120 | 1.000 | 15 | 48444614 | frameshift variant | G/- | delins | 1 | ||||
| rs1566900492 | 1.000 | 15 | 48452602 | frameshift variant | CA/- | delins | 1 | ||||
| rs1566900540 | 1.000 | 15 | 48452686 | splice acceptor variant | T/C | snv | 1 | ||||
| rs1566903914 | 1.000 | 15 | 48465582 | frameshift variant | -/T | delins | 1 | ||||
| rs1566904526 | 1.000 | 15 | 48467985 | frameshift variant | C/- | delins | 1 | ||||
| rs1566919637 | 1.000 | 15 | 48526168 | frameshift variant | G/- | delins | 1 | ||||
| rs1566938153 | 1.000 | 15 | 48613020 | frameshift variant | -/T | delins | 1 | ||||
| rs764203302 | 1.000 | 15 | 48452612 | missense variant | C/T | snv | 7.0E-06 | 1 | |||
| rs794728305 | 1.000 | 15 | 48492525 | stop gained | -/CTAG | delins | 1 | ||||
| rs794728306 | 1.000 | 15 | 48487347 | frameshift variant | -/AGGC | delins | 4.0E-06 | 1 | |||
| rs794728315 | 1.000 | 15 | 48441718 | splice donor variant | -/A | delins | 8.0E-06 | 1.4E-05 | 1 | ||
| rs1052480459 | 0.925 | 0.160 | 15 | 48437837 | stop gained | C/A;G | snv | 7.0E-06 | 2 | ||
| rs1057521102 | 0.925 | 0.160 | 15 | 48510088 | missense variant | C/A;T | snv | 2 | |||
| rs1057523406 | 0.925 | 0.160 | 15 | 48494209 | missense variant | C/A;G;T | snv | 2 | |||
| rs1057524458 | 0.925 | 0.160 | 15 | 48489988 | missense variant | C/G | snv | 2 | |||
| rs1060501017 | 0.925 | 0.160 | 15 | 48505136 | missense variant | A/C;G | snv | 2 | |||
| rs1060501021 | 0.925 | 0.160 | 15 | 48494210 | missense variant | A/G | snv | 2 | |||
| rs1060501022 | 0.925 | 0.160 | 15 | 48496214 | missense variant | A/G | snv | 2 | |||
| rs1060501023 | 0.925 | 0.160 | 15 | 48430758 | stop gained | G/A | snv | 2 | |||
| rs1060501029 | 0.925 | 0.160 | 15 | 48446909 | intron variant | T/C | snv | 2 |