Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs78352137 | 14 | 100454079 | intron variant | T/C | snv | 7.7E-02 | 2 | ||||
rs10144321 | 14 | 100416068 | intron variant | A/G | snv | 0.24 | 1 | ||||
rs12894936 | 14 | 100380654 | intron variant | T/C | snv | 0.55 | 1 |