Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs398062996 | 3 | 165193500 | intron variant | TCTG/- | delins | 0.10 | 1 | ||||
rs62282371 | 3 | 165193906 | intron variant | T/G | snv | 0.12 | 1 |
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs398062996 | 3 | 165193500 | intron variant | TCTG/- | delins | 0.10 | 1 | ||||
rs62282371 | 3 | 165193906 | intron variant | T/G | snv | 0.12 | 1 |