Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9568797 | 0.851 | 0.080 | 13 | 53039424 | intron variant | C/G;T | snv | 4 | |||
rs969599 | 0.851 | 0.080 | 8 | 18567221 | intron variant | G/A;T | snv | 4 | |||
rs9825420 | 0.851 | 0.080 | 3 | 37562521 | intron variant | T/G | snv | 0.18 | 4 | ||
rs9977018 | 0.851 | 0.080 | 21 | 41616809 | intergenic variant | T/G | snv | 0.24 | 4 |