Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs863224884 | 0.925 | 0.040 | 2 | 232770905 | missense variant | G/A | snv | 2 | |||
rs869320631 | 1.000 | 2 | 232771205 | stop gained | C/T | snv | 1 | ||||
rs143607153 | 1.000 | 2 | 232768552 | missense variant | A/G;T | snv | 6.4E-05 | 1 | |||
rs387906858 | 1.000 | 2 | 232768778 | stop gained | G/A;C | snv | 4.0E-06 | 1 | |||
rs786205550 | 1.000 | 2 | 232771004 | missense variant | A/G | snv | 7.0E-06 | 1 |