Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs761241711 | 0.925 | 0.080 | 18 | 31336524 | stop gained | T/C;G | snv | 1.1E-04 | 2 | ||
rs1057518788 | 0.925 | 0.120 | 18 | 31331787 | stop gained | G/T | snv | 2 | |||
rs1182196436 | 0.925 | 0.120 | 18 | 31326922 | stop gained | C/A;T | snv | 2 | |||
rs60399023 | 0.827 | 0.200 | 17 | 41586462 | missense variant | G/A;C | snv | 2 | |||
rs1114167422 | 0.776 | 0.320 | X | 154773148 | missense variant | A/G | snv | 11 | |||
rs104894226 | 0.658 | 0.560 | 11 | 534285 | missense variant | C/A;G;T | snv | 23 |