| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1133503 | 1.000 | 0.040 | 6 | 95606712 | 3 prime UTR variant | C/G;T | snv | 4 | |||
| rs754635 | 1.000 | 0.040 | 3 | 42263639 | splice region variant | C/G;T | snv | 0.84; 5.6E-06 | 3 | ||
| rs4076452 | 1.000 | 0.040 | 17 | 45778528 | intron variant | G/C | snv | 0.16 | 2 | ||
| rs10415555 | 1.000 | 0.040 | 19 | 33519283 | intron variant | A/G | snv | 0.19 | 1 | ||
| 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 | ||
| rs12061304 | 1.000 | 0.040 | 1 | 110695063 | intergenic variant | A/G | snv | 0.30 | 1 | ||
| rs13356494 | 1.000 | 0.040 | 5 | 135991866 | regulatory region variant | C/G;T | snv | 1 | |||
| rs1418688 | 1.000 | 0.040 | 6 | 71169166 | downstream gene variant | A/G;T | snv | 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 | |||
| rs17260539 | 1.000 | 0.040 | 9 | 12182545 | intergenic variant | G/A | snv | 6.6E-02 | 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 | ||
| rs2241165 | 1.000 | 0.040 | 2 | 170821869 | non coding transcript exon variant | C/T | snv | 0.63 | 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 |