| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12764899 | 1.000 | 0.040 | 10 | 102875346 | intron variant | G/A | snv | 0.21 | 4 | ||
| rs59721556 | 1.000 | 0.040 | 14 | 77646050 | TF binding site variant | G/A | snv | 0.19 | 3 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12764899 | 1.000 | 0.040 | 10 | 102875346 | intron variant | G/A | snv | 0.21 | 4 | ||
| rs59721556 | 1.000 | 0.040 | 14 | 77646050 | TF binding site variant | G/A | snv | 0.19 | 3 |