Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs34115320 | 7 | 149086845 | intron variant | TTTT/-;T;TT;TTT;TTTTT;TTTTTT | delins | 0.57 | 2 | ||||
rs564473618 | 7 | 149079267 | intron variant | G/C | snv | 1.3E-02 | 1 |