Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs727503109 | 0.752 | 0.320 | 12 | 25245277 | missense variant | T/C | snv | 17 | |||
rs104894360 | 0.724 | 0.560 | 12 | 25209904 | missense variant | T/A;C | snv | 14 | |||
rs104894365 | 0.827 | 0.320 | 12 | 25245345 | missense variant | C/T | snv | 9 | |||
rs104894366 | 0.776 | 0.400 | 12 | 25245284 | missense variant | G/A;C | snv | 9 | |||
rs104894359 | 0.851 | 0.200 | 12 | 25227346 | missense variant | C/G;T | snv | 5 | |||
rs730880471 | 0.851 | 0.280 | 12 | 25225709 | missense variant | C/T | snv | 4 | |||
rs727503110 | 0.882 | 0.160 | 12 | 25245320 | missense variant | T/A;C | snv | 3 | |||
rs104894364 | 0.925 | 0.160 | 12 | 25227351 | missense variant | G/A | snv | 2 | |||
rs1135401776 | 1.000 | 0.160 | 12 | 25225624 | missense variant | T/C | snv | 2 | |||
rs193929331 | 0.925 | 0.160 | 12 | 25245372 | missense variant | T/C | snv | 2 | |||
rs104894367 | 1.000 | 0.160 | 12 | 25209907 | missense variant | A/C | snv | 1 |