| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 121 | |
| rs2814778 | 0.763 | 0.360 | 1 | 159204893 | 5 prime UTR variant | T/C | snv | 0.25 | 24 | ||
| rs3123543 | 1 | 212617344 | intron variant | T/A;C | snv | 13 | |||||
| rs12239046 | 1 | 247438293 | intron variant | T/C | snv | 0.58 | 9 | ||||
| rs34599082 | 1 | 159205704 | missense variant | C/T | snv | 1.1E-02 | 9.9E-03 | 8 | |||
| rs201950044 | 1 | 161639782 | intergenic variant | G/T | snv | 5 | |||||
| rs2208568 | 1 | 235926855 | intergenic variant | T/A;C;G | snv | 5 | |||||
| rs3917914 | 1 | 36482287 | intron variant | G/A;T | snv | 5 | |||||
| rs3917932 | 1 | 36478315 | intron variant | C/G | snv | 0.59 | 5 | ||||
| rs663045 | 1 | 108200437 | 5 prime UTR variant | G/C | snv | 0.55 | 5 | ||||
| rs7550207 | 1 | 159205095 | intron variant | T/C | snv | 0.19 | 5 | ||||
| rs9436747 | 1 | 65445924 | intron variant | T/C | snv | 0.56 | 5 | ||||
| rs11204682 | 1 | 150623061 | intron variant | G/A;T | snv | 4 | |||||
| rs12752838 | 1 | 8853597 | upstream gene variant | A/G | snv | 0.54 | 4 | ||||
| rs17592479 | 1 | 226986191 | intron variant | T/A | snv | 0.41 | 4 | ||||
| rs301807 | 0.925 | 0.080 | 1 | 8424763 | intron variant | A/G;T | snv | 4 | |||
| rs34293785 | 1 | 65671509 | intergenic variant | T/C | snv | 4 | |||||
| rs41313381 | 1 | 78946283 | missense variant | C/A;T | snv | 1.9E-02; 3.3E-05 | 4 | ||||
| rs4844622 | 1 | 207860984 | intron variant | C/T | snv | 0.19 | 4 | ||||
| rs7537229 | 1 | 56440602 | intron variant | G/A | snv | 0.92 | 4 | ||||
| rs778387 | 1 | 56158423 | intron variant | C/A;G;T | snv | 4 | |||||
| rs1036332 | 1 | 199043349 | intron variant | A/C | snv | 0.70 | 3 | ||||
| rs114269697 | 1.000 | 0.040 | 1 | 64848529 | intron variant | C/A | snv | 7.3E-03 | 3 | ||
| rs159963 | 1.000 | 0.040 | 1 | 8444361 | intron variant | C/A | snv | 0.52 | 3 | ||
| rs2075995 | 1 | 23520972 | missense variant | C/A | snv | 0.45 | 0.39 | 3 |