| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs8034191 | 0.695 | 0.440 | 15 | 78513681 | intron variant | T/C | snv | 0.27 | 5 | ||
| rs2036534 | 0.827 | 0.080 | 15 | 78534606 | 3 prime UTR variant | T/C | snv | 0.26 | 3 | ||
| rs8031948 | 1.000 | 0.040 | 15 | 78523715 | intron variant | G/T | snv | 0.27 | 2 | ||
| rs3885951 | 1.000 | 0.040 | 15 | 78533575 | missense variant | A/G | snv | 7.5E-02 | 6.9E-02 | 2 | |
| rs28675338 | 1.000 | 0.040 | 15 | 78535289 | 3 prime UTR variant | C/T | snv | 2.4E-05 | 1 | ||
| rs58709975 | 1.000 | 0.040 | 15 | 78535290 | 3 prime UTR variant | TTT/-;T;TT;TTTT;TTTTT;TTTTTTT | delins | 1 | |||
| rs200049096 | 15 | 78510715 | intron variant | -/T | delins | 1.4E-05 | 1 | ||||
| rs931794 | 0.851 | 0.080 | 15 | 78533838 | 3 prime UTR variant | G/A;C | snv | 1 | |||
| rs7163730 | 15 | 78522339 | intron variant | A/G | snv | 0.25 | 1 | ||||
| rs7164594 | 15 | 78510715 | intron variant | C/T | snv | 0.32 | 1 | ||||
| rs12591557 | 15 | 78519390 | intron variant | A/G | snv | 0.33 | 1 | ||||
| rs9788721 | 1.000 | 0.040 | 15 | 78510527 | intron variant | C/T | snv | 0.65 | 1 | ||
| rs4461039 | 15 | 78525105 | intron variant | A/T | snv | 0.27 | 1 | ||||
| rs10519203 | 0.851 | 0.080 | 15 | 78521704 | intron variant | G/A | snv | 0.67 | 1 | ||
| rs9788682 | 15 | 78510244 | intron variant | G/A;T | snv | 1 |