Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11230563 | 0.790 | 0.360 | 11 | 61008737 | missense variant | C/G;T | snv | 4.2E-06; 0.31 | 8 | ||
rs17824933 | 1.000 | 0.080 | 11 | 60993140 | intron variant | C/A;G | snv | 1 | |||
rs112852289 | 1.000 | 0.080 | 11 | 61008833 | frameshift variant | -/T | ins | 5.1E-06; 5.1E-06 | 1 | ||
rs2074225 | 1.000 | 0.080 | 11 | 61008834 | missense variant | C/T | snv | 0.53 | 0.58 | 1 | |
rs386754116 | 1.000 | 0.080 | 11 | 61008834 | missense variant | CG/TC | mnv | 1 |