Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1557612719 | 1.000 | 0.160 | 1 | 43930201 | stop lost | G/T | snv | 1 | |||
rs387906943 | 1.000 | 0.160 | 1 | 43736300 | missense variant | C/A | snv | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1557612719 | 1.000 | 0.160 | 1 | 43930201 | stop lost | G/T | snv | 1 | |||
rs387906943 | 1.000 | 0.160 | 1 | 43736300 | missense variant | C/A | snv | 1 |