Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397516830 | 0.827 | 0.160 | 3 | 12604182 | missense variant | A/C;G;T | snv | 5 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397516830 | 0.827 | 0.160 | 3 | 12604182 | missense variant | A/C;G;T | snv | 5 |