| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28933090 | 0.925 | 0.160 | 1 | 156115172 | missense variant | T/A;G | snv | 3 | |||
| rs267607646 | 1.000 | 0.080 | 1 | 156115265 | frameshift variant | -/G | delins | 2 | |||
| rs794728589 | 1.000 | 0.080 | 1 | 156115275 | splice donor variant | G/A;C | snv | 2 | |||
| rs794728597 | 1 | 156130624 | inframe deletion | AAG/- | delins | 1 | |||||
| rs58917027 | 1.000 | 0.120 | 1 | 156130708 | missense variant | A/C;G | snv | 2 | |||
| rs876657650 | 1 | 156130736 | frameshift variant | A/- | del | 1 | |||||
| rs28933093 | 0.882 | 0.160 | 1 | 156130741 | missense variant | G/A | snv | 5 | |||
| rs267607594 | 0.925 | 0.120 | 1 | 156130745 | missense variant | T/C | snv | 3 | |||
| rs397517904 | 1 | 156130774 | splice donor variant | G/A;C;T | snv | 1 | |||||
| rs59026483 | 0.827 | 0.160 | 1 | 156134457 | missense variant | C/T | snv | 7.0E-06 | 7 | ||
| rs57045855 | 0.882 | 0.040 | 1 | 156134464 | missense variant | A/G;T | snv | 6 | |||
| rs28933091 | 0.882 | 0.160 | 1 | 156134474 | missense variant | C/A;G | snv | 4 | |||
| rs61195471 | 0.827 | 0.160 | 1 | 156134496 | missense variant | G/A | snv | 6 | |||
| rs28933092 | 1.000 | 0.040 | 1 | 156134497 | missense variant | A/G;T | snv | 2 | |||
| rs794728591 | 1.000 | 0.080 | 1 | 156134811 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 2 | |
| rs58034145 | 0.827 | 0.160 | 1 | 156134830 | missense variant | A/C | snv | 10 | |||
| rs60682848 | 0.790 | 0.200 | 1 | 156134838 | stop gained | C/T | snv | 7.0E-06 | 11 | ||
| rs267607573 | 1.000 | 0.080 | 1 | 156134865 | stop gained | C/T | snv | 2 | |||
| rs730880132 | 1 | 156134875 | missense variant | T/C | snv | 1 | |||||
| rs397517906 | 0.925 | 0.080 | 1 | 156134890 | missense variant | C/T | snv | 8.0E-06 | 3 | ||
| rs397517908 | 1 | 156134927 | frameshift variant | C/- | delins | 1 | |||||
| rs794728593 | 1 | 156134933 | synonymous variant | G/A | snv | 7.0E-06 | 1 | ||||
| rs58978449 | 1 | 156134943 | inframe deletion | AAG/- | delins | 1 | |||||
| rs397517909 | 1 | 156134949 | stop gained | G/T | snv | 1 | |||||
| rs267607593 | 1 | 156134964 | missense variant | T/C | snv | 1 |