| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10919019 | 1.000 | 0.040 | 1 | 168926275 | intron variant | T/A;C | snv | 1 | |||
| rs114101204 | 1 | 169056816 | intron variant | G/A | snv | 1.3E-02 | 1 | ||||
| rs114964168 | 1 | 169063639 | intron variant | C/T | snv | 1.3E-02 | 1 | ||||
| rs17514217 | 1.000 | 0.040 | 1 | 168920169 | intron variant | T/A | snv | 9.6E-02 | 1 | ||
| rs17514245 | 1.000 | 0.040 | 1 | 168920319 | intron variant | A/G | snv | 0.10 | 1 | ||
| rs2146204 | 1 | 168904861 | intron variant | A/C | snv | 0.13 | 1 | ||||
| rs6427160 | 1.000 | 0.040 | 1 | 168922943 | intron variant | T/C | snv | 0.37 | 1 | ||
| rs7530207 | 1.000 | 0.040 | 1 | 168921182 | intron variant | G/C | snv | 0.12 | 1 | ||
| rs78516619 | 1 | 168920135 | intron variant | A/G | snv | 7.8E-03 | 1 | ||||
| rs911892 | 1.000 | 0.040 | 1 | 168922386 | intron variant | A/C | snv | 0.86 | 1 | ||
| rs973608 | 1.000 | 0.040 | 1 | 168919708 | intron variant | C/T | snv | 0.13 | 1 |