Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs80356616 | 0.732 | 0.360 | 11 | 17387917 | missense variant | C/T | snv | 19 | |||
rs80356624 | 0.752 | 0.240 | 11 | 17387490 | missense variant | C/A;T | snv | 16 | |||
rs80356618 | 0.807 | 0.200 | 11 | 17387595 | missense variant | C/A;T | snv | 8 | |||
rs80356625 | 0.827 | 0.280 | 11 | 17387491 | missense variant | G/A | snv | 6 | |||
rs80356615 | 0.851 | 0.240 | 11 | 17387934 | missense variant | C/T | snv | 4 | |||
rs80356637 | 0.851 | 0.240 | 11 | 17470119 | missense variant | A/C;G | snv | 4 | |||
rs80356617 | 0.882 | 0.160 | 11 | 17387916 | missense variant | A/C | snv | 3 | |||
rs80356620 | 0.882 | 0.160 | 11 | 17387593 | missense variant | T/G | snv | 3 | |||
rs387906783 | 0.925 | 0.160 | 11 | 17387913 | missense variant | A/G;T | snv | 2 |