| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
| rs1057519021 | 0.925 | 0.120 | 5 | 151267341 | stop gained | G/T | snv | 2 | |||
| rs104893892 | 1.000 | 0.120 | 5 | 151267375 | missense variant | G/A;C;T | snv | 9.5E-05; 4.0E-06 | 1 | ||
| rs104893897 | 1.000 | 0.120 | 5 | 151259833 | stop gained | G/T | snv | 1 | |||
| rs1057519022 | 1.000 | 0.120 | 5 | 151266729 | splice acceptor variant | A/T | snv | 1 | |||
| rs137852797 | 1.000 | 0.120 | 5 | 151266899 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs730882196 | 1.000 | 0.120 | 5 | 151259837 | missense variant | C/T | snv | 1 |