Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs531184891 | 11 | 67129907 | intron variant | AA/-;A;AAA | delins | 5.0E-02 | 3 | ||||
rs7952436 | 11 | 67257063 | 3 prime UTR variant | C/T | snv | 4.7E-02 | 3 | ||||
rs12785905 | 1.000 | 0.080 | 11 | 67184494 | intron variant | G/C | snv | 3.4E-02 | 1 | ||
rs552846225 | 11 | 67145999 | intron variant | T/-;TT;TTT | delins | 1 | |||||
rs56088284 | 11 | 67132148 | intron variant | A/G | snv | 4.8E-02 | 1 |