Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs886039469 | 0.701 | 0.560 | 10 | 76891709 | missense variant | T/C | snv | 34 | |||
rs1565091862 | 0.925 | 0.160 | 10 | 76944829 | missense variant | T/C | snv | 4 | |||
rs137853333 | 0.925 | 0.080 | 10 | 77090433 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
rs863224885 | 1.000 | 0.080 | 10 | 77110250 | missense variant | T/C | snv | 1 | |||
rs762705295 | 1.000 | 10 | 77012033 | frameshift variant | A/-;AA | delins | 1 |