Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7023923 | 0.851 | 0.120 | 9 | 111163254 | intron variant | T/A;C | snv | 4 | |||
rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 187 | ||
rs1557043622 | 0.695 | 0.400 | X | 48909843 | missense variant | C/A | snv | 46 |