| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs104894073 | 0.827 | 0.080 | 8 | 11750213 | missense variant | G/A;C;T | snv | 8 | |||
| rs870142 | 0.851 | 0.120 | 4 | 4646320 | intron variant | C/G;T | snv | 7 | |||
| rs387906772 | 1.000 | 0.080 | 8 | 11755064 | missense variant | A/G;T | snv | 3 |