| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs144292455 | 0.882 | 0.040 | 4 | 103656258 | stop gained | C/T | snv | 3.1E-04 | 3.8E-04 | 3 | |
| rs121918124 | 1.000 | 4 | 103719398 | missense variant | C/G;T | snv | 1 | ||||
| rs121918125 | 1.000 | 4 | 103591515 | missense variant | G/A;C | snv | 4.0E-06 | 1 | |||
| rs150288991 | 1.000 | 4 | 103589989 | missense variant | C/G;T | snv | 1.1E-04 | 2.9E-04 | 1 | ||
| rs200148989 | 1.000 | 4 | 103591536 | missense variant | T/C | snv | 4.0E-06 | 1 | |||
| rs397515483 | 1.000 | 4 | 103656316 | missense variant | A/G | snv | 1 | ||||
| rs764659822 | 1.000 | 4 | 103658260 | missense variant | G/A | snv | 3.2E-05 | 1 |