Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7124972 | 11 | 81291756 | intron variant | C/T | snv | 7.7E-02 | 1 | ||||
rs7704641 | 5 | 5260570 | intron variant | G/A | snv | 0.37 | 1 | ||||
rs4767841 | 12 | 119724394 | intron variant | G/A | snv | 0.55 | 1 | ||||
rs150663673 | 10 | 25118280 | intron variant | G/A | snv | 1.3E-02 | 1 | ||||
rs112673195 | 12 | 31908519 | intron variant | G/A;C | snv | 1 | |||||
rs72881251 | 18 | 25094696 | intron variant | T/C | snv | 0.14 | 1 |