Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11098964 | 0.827 | 0.120 | 4 | 79966815 | intron variant | A/G;T | snv | 5 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11098964 | 0.827 | 0.120 | 4 | 79966815 | intron variant | A/G;T | snv | 5 |