Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11193085 | 10 | 106873848 | intron variant | G/A | snv | 8.8E-02 | 3 | ||||
rs12247406 | 10 | 106996746 | intron variant | G/A | snv | 1.3E-02 | 3 | ||||
rs11813704 | 10 | 107102114 | intron variant | G/T | snv | 3.1E-02 | 2 | ||||
rs7910584 | 1.000 | 0.040 | 10 | 106607970 | intron variant | C/A | snv | 0.65 | 1 | ||
rs2756231 | 10 | 106706654 | intron variant | C/T | snv | 0.98 | 0.97 | 1 |