| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121908130 | 0.882 | 0.160 | 15 | 77031225 | missense variant | G/A | snv | 3 | |||
| rs28939089 | 0.882 | 0.160 | 15 | 77032304 | missense variant | G/A;C | snv | 3 | |||
| rs368652620 | 0.925 | 0.160 | 8 | 93709810 | stop gained | C/G;T | snv | 4.0E-06; 2.4E-05 | 2 | ||
| rs104895111 | 0.925 | 0.160 | 16 | 3254317 | stop gained | C/A;G;T | snv | 4.0E-06 | 2 | ||
| rs565817241 | 1.000 | 0.120 | 7 | 42045434 | missense variant | G/A;C | snv | 4.0E-06; 1.6E-05 | 1 | ||
| rs868749744 | 1.000 | 0.120 | 2 | 112833417 | synonymous variant | C/T | snv | 1 | |||
| rs34240327 | 1.000 | 0.120 | 15 | 77032329 | missense variant | G/A;C | snv | 8.2E-03 | 1 |