Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs137854612 | 0.851 | 0.120 | 3 | 38560170 | missense variant | C/T | snv | 4 | |||
rs869025458 | 1.000 | 0.080 | 1 | 156115272 | missense variant | GC/AG | mnv | 1 | |||
rs121434627 | 1.000 | 0.080 | 19 | 35033550 | stop gained | G/A;C;T | snv | 1.2E-05; 4.0E-06 | 1 | ||
rs267607029 | 0.925 | 0.080 | 19 | 35033828 | stop gained | G/A | snv | 1 |