Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113994152 | 0.790 | 0.160 | 17 | 75522000 | missense variant | G/T | snv | 9.0E-04 | 9.0E-04 | 11 | |
rs587784477 | 17 | 75524342 | missense variant | T/C | snv | 1 | |||||
rs587784475 | 17 | 75522219 | stop gained | G/C;T | snv | 1 | |||||
rs587784479 | 17 | 75521461 | frameshift variant | AC/- | delins | 1 | |||||
rs587784478 | 17 | 75516561 | start lost | A/C | snv | 7.3E-06 | 1 | ||||
rs587784476 | 17 | 75523684 | frameshift variant | C/- | del | 1 |