| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12047002 | 1.000 | 0.040 | 1 | 48104794 | intron variant | G/T | snv | 0.18 | 1 | ||
| rs17428691 | 1.000 | 0.040 | 1 | 48101445 | intron variant | G/A | snv | 8.8E-02 | 1 | ||
| rs17468833 | 1.000 | 0.040 | 1 | 48098595 | intron variant | C/T | snv | 0.47 | 1 | ||
| rs2073293 | 1.000 | 0.040 | 1 | 48104461 | non coding transcript exon variant | G/A | snv | 0.22 | 1 | ||
| rs10888596 | 1.000 | 0.040 | 1 | 48103000 | non coding transcript exon variant | T/G | snv | 0.48 | 1 | ||
| rs17299092 | 1.000 | 0.040 | 1 | 48109438 | intron variant | A/T | snv | 4.2E-02 | 1 | ||
| rs17468972 | 1.000 | 0.040 | 1 | 48102728 | non coding transcript exon variant | T/C;G | snv | 1 |