| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6054 | 1.000 | 0.080 | 4 | 154568456 | missense variant | C/T | snv | 2.4E-03 | 2.7E-03 | 6 | |
| rs148685782 | 1.000 | 0.080 | 4 | 154611883 | missense variant | G/C | snv | 1.9E-03 | 2.2E-03 | 4 | |
| rs75848804 | 0.882 | 0.080 | 4 | 154604995 | missense variant | G/A;C;T | snv | 4 | |||
| rs121909621 | 0.925 | 0.120 | 4 | 154569703 | missense variant | T/G | snv | 2 | |||
| rs121909622 | 0.925 | 0.120 | 4 | 154570463 | missense variant | G/A | snv | 2 | |||
| rs121909625 | 0.925 | 0.080 | 4 | 154565832 | stop gained | C/T | snv | 1.2E-05 | 5.6E-05 | 2 | |
| rs755117226 | 1.000 | 0.080 | 4 | 154587520 | stop gained | G/A | snv | 8.0E-06 | 2.1E-05 | 1 | |
| rs121909623 | 1.000 | 0.080 | 4 | 154567688 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs121909624 | 1.000 | 0.080 | 4 | 154567707 | missense variant | T/A;C | snv | 1 | |||
| rs1553965519 | 1.000 | 0.080 | 4 | 154606812 | stop gained | C/T | snv | 1 |