| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs514716 | 1.000 | 0.080 | 9 | 3929424 | intron variant | C/A;T | snv | 1 | |||
| rs1983753 | 9 | 4160364 | intron variant | G/A;C | snv | 1 | |||||
| rs7020673 | 0.882 | 0.200 | 9 | 4291747 | intron variant | C/A;G | snv | 1 | |||
| rs6476839 | 0.925 | 0.120 | 9 | 4290823 | intron variant | A/C;T | snv | 1 | |||
| rs1017568 | 1.000 | 0.080 | 9 | 3948365 | intron variant | T/C;G | snv | 1 | |||
| rs736893 | 0.925 | 0.040 | 9 | 4217028 | intron variant | G/A;C | snv | 1 | |||
| rs501461 | 9 | 4039727 | intron variant | G/A;T | snv | 1 | |||||
| rs4741893 | 9 | 4123284 | intron variant | G/A;C | snv | 1 | |||||
| rs4237150 | 9 | 4290085 | intron variant | G/A;C;T | snv | 1 | |||||
| rs10974256 | 9 | 3952892 | intron variant | G/A;C | snv | 1 | |||||
| rs28558845 | 9 | 4334791 | intron variant | G/A;C;T | snv | 1 |