Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6119267 | 20 | 32576112 | intron variant | C/A;G | snv | 3 | |||||
rs12480732 | 20 | 32603213 | intron variant | C/T | snv | 0.19 | 2 | ||||
rs7266642 | 20 | 32593666 | intron variant | A/G | snv | 0.50 | 1 | ||||
rs67696533 | 20 | 32585560 | intron variant | G/A;T | snv | 1 |