Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113994139 | 0.925 | 0.120 | 17 | 42322474 | missense variant | C/T | snv | 3 | |||
rs193922716 | 0.925 | 0.120 | 17 | 42333719 | missense variant | G/A | snv | 3 | |||
rs193922721 | 0.925 | 0.120 | 17 | 42322413 | missense variant | T/C | snv | 3 | |||
rs886039434 | 0.925 | 0.120 | 17 | 42322404 | missense variant | A/G | snv | 3 |