Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs653178 | 0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 | 23 | ||
rs913678 | 0.882 | 0.240 | 20 | 50338887 | regulatory region variant | T/C | snv | 0.51 | 5 | ||
rs13277237 | 8 | 129592317 | intron variant | G/A | snv | 0.53 | 4 | ||||
rs1991866 | 8 | 129611859 | intron variant | G/A;C | snv | 3 |