| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs684214 | 17 | 42544897 | intron variant | C/T | snv | 0.20 | 1 | ||||
| rs752131463 | 1.000 | 17 | 42541070 | frameshift variant | C/- | delins | 8.0E-06 | 1 | |||
| rs796052122 | 1.000 | 17 | 42543214 | missense variant | T/C | snv | 8.0E-06 | 7.0E-06 | 1 | ||
| rs2071046 | 1.000 | 0.040 | 17 | 42537595 | intron variant | G/A;C | snv | 4.2E-06; 0.74 | 1 | ||
| rs104894590 | 0.925 | 0.120 | 17 | 42544027 | missense variant | G/A;T | snv | 1.6E-05 | 2 | ||
| rs104894591 | 0.925 | 0.120 | 17 | 42543882 | stop gained | C/G;T | snv | 4.4E-06; 2.2E-05 | 2 | ||
| rs104894599 | 0.925 | 0.120 | 17 | 42536416 | missense variant | C/A;G;T | snv | 7.1E-06 | 2 | ||
| rs118204024 | 0.925 | 0.120 | 17 | 42536414 | missense variant | T/C | snv | 2 | |||
| rs1244655820 | 0.925 | 0.120 | 17 | 42543603 | stop gained | C/T | snv | 7.0E-06 | 2 | ||
| rs147036053 | 0.925 | 0.120 | 17 | 42543906 | missense variant | G/A | snv | 1.3E-05 | 4.2E-05 | 2 | |
| rs368687817 | 1.000 | 0.120 | 17 | 42543079 | missense variant | C/T | snv | 3.3E-05 | 4.2E-05 | 2 | |
| rs746006696 | 0.925 | 0.120 | 17 | 42543997 | missense variant | C/T | snv | 4.1E-06 | 7.0E-06 | 2 | |
| rs768814260 | 0.925 | 0.120 | 17 | 42543247 | missense variant | A/G | snv | 2.4E-05 | 7.0E-06 | 2 | |
| rs86312 | 0.925 | 0.120 | 17 | 42544215 | missense variant | C/A;G;T | snv | 1.8E-02; 0.91; 8.1E-06 | 2 | ||
| rs1013345784 | 1.000 | 0.120 | 17 | 42536274 | start lost | T/C;G | snv | 1 | |||
| rs104894593 | 1.000 | 0.120 | 17 | 42543934 | missense variant | G/A | snv | 1 | |||
| rs104894594 | 1.000 | 0.120 | 17 | 42543933 | missense variant | C/A;T | snv | 4.2E-06 | 1 | ||
| rs104894595 | 1.000 | 0.120 | 17 | 42543568 | missense variant | C/T | snv | 2.0E-05 | 2.1E-05 | 1 | |
| rs104894596 | 1.000 | 0.120 | 17 | 42543450 | missense variant | C/A;T | snv | 2.7E-05 | 1.4E-05 | 1 | |
| rs104894597 | 1.000 | 0.120 | 17 | 42543699 | missense variant | C/T | snv | 3.2E-05 | 3.5E-05 | 1 | |
| rs104894600 | 1.000 | 0.120 | 17 | 42541125 | missense variant | T/C | snv | 1 | |||
| rs104894601 | 1.000 | 0.120 | 17 | 42538691 | missense variant | C/T | snv | 3.2E-05 | 7.0E-06 | 1 | |
| rs1052471595 | 1.000 | 0.120 | 17 | 42541119 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs1180591588 | 1.000 | 0.120 | 17 | 42543068 | frameshift variant | C/- | delins | 1 | |||
| rs118204025 | 1.000 | 0.120 | 17 | 42541127 | missense variant | C/G | snv | 8.0E-06 | 1 |