| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10454453 | 1.000 | 0.040 | 1 | 66206849 | intron variant | C/A | snv | 0.48 | 1 | ||
| rs10801152 | 1.000 | 0.040 | 1 | 192792174 | intron variant | A/T | snv | 0.31 | 1 | ||
| rs10875995 | 1.000 | 0.040 | 12 | 50068355 | intron variant | T/A;C | snv | 1 | |||
| rs10879357 | 1.000 | 0.040 | 12 | 72020783 | intron variant | A/G | snv | 0.59 | 1 | ||
| rs11060369 | 1.000 | 0.040 | 12 | 129475652 | intron variant | A/C | snv | 0.41 | 1 | ||
| rs11763020 | 1.000 | 0.040 | 7 | 1020652 | intron variant | C/T | snv | 0.12 | 1 | ||
| rs11805657 | 1.000 | 0.040 | 1 | 240955726 | intron variant | T/C | snv | 0.87 | 1 | ||
| rs144783209 | 1.000 | 0.040 | 4 | 145482377 | intron variant | G/C;T | snv | 1 | |||
| rs1487275 | 1.000 | 0.040 | 12 | 72016512 | intron variant | C/A | snv | 0.71 | 1 | ||
| rs16938184 | 1.000 | 0.040 | 11 | 45179068 | intron variant | G/A;C | snv | 1 | |||
| rs1819741 | 1.000 | 0.040 | 1 | 192815708 | intron variant | T/A;C | snv | 1 | |||
| rs191260602 | 1.000 | 0.040 | 4 | 157140489 | intron variant | A/G | snv | 7.7E-03 | 1 | ||
| rs2039391 | 1.000 | 0.040 | 9 | 20714015 | intron variant | C/T | snv | 0.86 | 1 | ||
| rs2770292 | 1.000 | 0.040 | 13 | 46860971 | intron variant | C/G | snv | 0.18 | 1 | ||
| rs324891 | 1.000 | 0.040 | 5 | 88616114 | intron variant | C/T | snv | 4.2E-04 | 1 | ||
| rs3742278 | 1.000 | 0.040 | 13 | 46845442 | intron variant | A/G | snv | 0.19 | 1 | ||
| rs3816995 | 1.000 | 0.040 | 17 | 73339121 | intron variant | G/A | snv | 0.40 | 1 | ||
| rs4583306 | 1.000 | 0.040 | 17 | 30211697 | intron variant | A/G | snv | 0.37 | 1 | ||
| rs4795942 | 1.000 | 0.040 | 17 | 34584149 | intron variant | C/T | snv | 0.72 | 1 | ||
| rs4804833 | 1.000 | 0.040 | 19 | 7905750 | intron variant | A/G;T | snv | 1 | |||
| rs4977831 | 1.000 | 0.040 | 9 | 20713069 | intron variant | A/G;T | snv | 1 | |||
| rs6502892 | 1.000 | 0.040 | 17 | 1714314 | intron variant | T/C;G | snv | 1 | |||
| rs7301616 | 1.000 | 0.040 | 12 | 60214608 | intron variant | C/T | snv | 0.96 | 1 | ||
| rs7309727 | 1.000 | 0.040 | 12 | 129470814 | intron variant | T/C | snv | 0.75 | 1 | ||
| rs8076112 | 1.000 | 0.040 | 17 | 1708905 | intron variant | A/C;G | snv | 0.15 | 1 |