Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
rs1695 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 188 | |
rs74315450 | 0.851 | 0.120 | 21 | 34859485 | missense variant | C/T | snv | 5 | |||
rs7729269 | 0.925 | 0.040 | 5 | 113384697 | intron variant | T/C | snv | 0.17 | 3 |