| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs201701502 | 0.851 | 0.080 | 1 | 162775837 | missense variant | C/G;T | snv | 1.5E-04 | 2.1E-05 | 5 | |
| rs765660823 | 0.882 | 0.200 | 1 | 162778720 | missense variant | A/C | snv | 1.9E-04 | 4 | ||
| rs267598140 | 0.925 | 0.080 | 1 | 162778600 | missense variant | T/A;G | snv | 2 | |||
| rs144594252 | 0.882 | 0.080 | 1 | 162754625 | missense variant | C/G | snv | 6.8E-05 | 5.6E-05 | 2 | |
| rs115169993 | 1.000 | 0.040 | 1 | 162772032 | missense variant | G/A | snv | 7.8E-04 | 2.9E-03 | 1 | |
| rs121964863 | 1.000 | 0.120 | 1 | 162776341 | missense variant | C/T | snv | 1 | |||
| rs121964865 | 1.000 | 0.120 | 1 | 162776225 | missense variant | C/A;T | snv | 4.0E-06 | 1 | ||
| rs397514747 | 1.000 | 0.120 | 1 | 162754775 | missense variant | G/A | snv | 1 |