Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1462083784 | 20 | 23049251 | missense variant | C/T | snv | 7.3E-06 | 1 | ||||
rs776339896 | 13 | 113129584 | missense variant | G/A | snv | 4.0E-06 | 1 | ||||
rs387906482 | 1.000 | 0.080 | X | 139561716 | missense variant | T/C | snv | 9.4E-06 | 2 |