Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1554846212 | 0.851 | 0.160 | 10 | 75030037 | missense variant | C/T | snv | 9 | |||
rs1553517323 | 1.000 | 2 | 189085204 | missense variant | C/A | snv | 4 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1554846212 | 0.851 | 0.160 | 10 | 75030037 | missense variant | C/T | snv | 9 | |||
rs1553517323 | 1.000 | 2 | 189085204 | missense variant | C/A | snv | 4 |