| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 72 | |
| rs121913059 | 0.716 | 0.280 | 1 | 196747245 | missense variant | C/T | snv | 1.4E-04 | 1.9E-04 | 16 | |
| rs121913061 | 1.000 | 0.080 | 1 | 196690125 | stop gained | C/T | snv | 1 | |||
| rs121913062 | 1.000 | 0.080 | 1 | 196743552 | missense variant | G/T | snv | 6.8E-05 | 4.2E-05 | 1 | |
| rs387906550 | 1.000 | 0.080 | 1 | 196673968 | splice region variant | T/G | snv | 1 |