Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs868443937 | 1.000 | 0.040 | 13 | 110715751 | missense variant | G/C;T | snv | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs868443937 | 1.000 | 0.040 | 13 | 110715751 | missense variant | G/C;T | snv | 1 |