Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs111929350 | 1.000 | 0.160 | 15 | 48452603 | missense variant | C/A;G;T | snv | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs111929350 | 1.000 | 0.160 | 15 | 48452603 | missense variant | C/A;G;T | snv | 1 |