| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6800135 | 0.925 | 0.040 | 3 | 81601337 | intron variant | C/T | snv | 0.64 | 2 | ||
| rs3849570 | 3 | 81742961 | intron variant | C/A | snv | 0.39 | 2 | ||||
| rs17410360 | 1.000 | 0.040 | 3 | 81519143 | intron variant | A/T | snv | 3.4E-02 | 1 | ||
| rs7622930 | 1.000 | 0.040 | 3 | 81501369 | intron variant | A/C;T | snv | 0.16 | 1 | ||
| rs9862299 | 1.000 | 0.040 | 3 | 81494898 | intron variant | T/C | snv | 0.14 | 1 | ||
| rs7622741 | 1.000 | 0.040 | 3 | 81501164 | intron variant | A/G | snv | 0.30 | 1 | ||
| rs7649028 | 1.000 | 0.040 | 3 | 81497265 | intron variant | C/T | snv | 0.30 | 1 | ||
| rs820274 | 1.000 | 0.040 | 3 | 81496552 | intron variant | A/G | snv | 0.97 | 1 | ||
| rs2307058 | 1.000 | 0.040 | 3 | 81537288 | intron variant | G/A | snv | 0.29 | 1 | ||
| rs13082940 | 1.000 | 0.040 | 3 | 81498113 | intron variant | A/G | snv | 0.22 | 1 | ||
| rs9815059 | 1.000 | 0.040 | 3 | 81489477 | downstream gene variant | C/T | snv | 0.30 | 1 | ||
| rs17019039 | 1.000 | 0.040 | 3 | 81503708 | intron variant | G/A | snv | 0.13 | 1 | ||
| rs843940 | 1.000 | 0.040 | 3 | 81497971 | intron variant | T/A | snv | 0.35 | 1 | ||
| rs6769230 | 1.000 | 0.040 | 3 | 81511942 | intron variant | C/A;T | snv | 1 | |||
| rs9842657 | 1.000 | 0.040 | 3 | 81516069 | intron variant | T/C;G | snv | 1 | |||
| rs2372908 | 1.000 | 0.040 | 3 | 81541145 | intron variant | G/C | snv | 0.66 | 1 | ||
| rs12637192 | 1.000 | 0.040 | 3 | 81534447 | intron variant | G/T | snv | 9.2E-02 | 1 | ||
| rs9821673 | 1.000 | 0.040 | 3 | 81545430 | intron variant | G/A | snv | 0.16 | 1 | ||
| rs6789701 | 1.000 | 0.040 | 3 | 81517504 | intron variant | G/A | snv | 8.8E-02 | 1 | ||
| rs3772882 | 3 | 81759451 | intron variant | C/A | snv | 0.45 | 1 |