Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs368869806 | 0.614 | 0.480 | 9 | 95485875 | splice acceptor variant | C/T | snv | 4.0E-06 | 7.0E-06 | 97 | |
rs267606826 | 0.708 | 0.520 | 14 | 28767903 | stop gained | C/A;G;T | snv | 38 | |||
rs1057524820 | 0.776 | 0.280 | 12 | 51765746 | missense variant | G/A;T | snv | 33 | |||
rs1555968941 | 0.752 | 0.280 | 12 | 2653847 | missense variant | G/A;C | snv | 31 |