| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs61734645 | 1.000 | 0.040 | 3 | 52349827 | intron variant | A/G | snv | 4.9E-02 | 1 | ||
| rs62250661 | 1.000 | 0.040 | 3 | 85402044 | intron variant | C/A | snv | 0.38 | 1 | ||
| rs62253085 | 1.000 | 0.040 | 3 | 85344618 | intron variant | A/G;T | snv | 1 | |||
| rs6445541 | 1.000 | 0.040 | 3 | 52846112 | intron variant | G/T | snv | 0.37 | 1 | ||
| rs6807666 | 1.000 | 0.040 | 3 | 85545278 | intron variant | A/C | snv | 0.59 | 1 | ||
| rs7355953 | 1.000 | 0.040 | 3 | 85742987 | intron variant | T/A;C | snv | 0.16 | 1 | ||
| rs818219 | 1.000 | 0.040 | 3 | 85325439 | intron variant | T/C | snv | 0.58 | 1 | ||
| rs9811546 | 1.000 | 0.040 | 3 | 85342522 | intron variant | G/A | snv | 0.26 | 1 | ||
| rs9828595 | 1.000 | 0.040 | 3 | 85843897 | intron variant | T/A;C;G | snv | 1 | |||
| rs9836178 | 1.000 | 0.040 | 3 | 52891387 | intron variant | T/A;C | snv | 1 | |||
| rs9837462 | 1.000 | 0.040 | 3 | 85109415 | intron variant | C/A | snv | 0.25 | 1 | ||
| rs9861237 | 1.000 | 0.040 | 3 | 85353319 | intron variant | T/C | snv | 0.39 | 1 | ||
| rs9870384 | 1.000 | 0.040 | 3 | 84960666 | intron variant | C/T | snv | 0.29 | 1 | ||
| rs104893877 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 59 | |||
| rs2071559 | 0.667 | 0.680 | 4 | 55126199 | upstream gene variant | A/G | snv | 0.53 | 26 | ||
| rs1870377 | 0.695 | 0.520 | 4 | 55106807 | missense variant | T/A | snv | 0.22 | 0.20 | 25 | |
| rs5522 | 0.732 | 0.320 | 4 | 148436323 | missense variant | C/T | snv | 0.88 | 0.89 | 19 | |
| rs356219 | 0.776 | 0.240 | 4 | 89716450 | intron variant | G/A | snv | 0.54 | 9 | ||
| rs356200 | 0.882 | 0.160 | 4 | 89747463 | intron variant | T/C | snv | 0.44 | 4 | ||
| rs17536211 | 1.000 | 0.040 | 4 | 46085716 | intron variant | A/C | snv | 0.14 | 3 | ||
| rs10005233 | 1.000 | 0.040 | 4 | 89822180 | 3 prime UTR variant | C/T | snv | 0.58 | 0.59 | 1 | |
| rs10034259 | 1.000 | 0.040 | 4 | 104012596 | intron variant | A/C | snv | 0.19 | 1 | ||
| rs57360718 | 1.000 | 0.040 | 4 | 118015036 | intergenic variant | T/C | snv | 0.10 | 1 | ||
| rs6851494 | 1.000 | 0.040 | 4 | 118133633 | intron variant | G/A;C;T | snv | 1 | |||
| rs6295 | 0.645 | 0.200 | 5 | 63962738 | intron variant | C/G | snv | 0.49 | 40 |