Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs727502818 | 0.790 | 0.160 | 11 | 17772053 | missense variant | G/A | snv | 26 | |||
rs1554991378 | 1.000 | 0.040 | 11 | 17772356 | missense variant | C/T | snv | 1 | |||
rs1565162623 | 1.000 | 0.040 | 11 | 17771785 | missense variant | A/G | snv | 1 |