Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs114090132 | 1.000 | 0.080 | 5 | 135810905 | intron variant | C/G;T | snv | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs114090132 | 1.000 | 0.080 | 5 | 135810905 | intron variant | C/G;T | snv | 1 |