Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 121 | |
rs7574865 | 0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 | 59 | ||
rs10488631 | 0.742 | 0.280 | 7 | 128954129 | upstream gene variant | T/C | snv | 9.0E-02 | 13 | ||
rs11889341 | 0.732 | 0.480 | 2 | 191079016 | intron variant | C/T | snv | 0.21 | 12 | ||
rs2205960 | 0.763 | 0.400 | 1 | 173222336 | intergenic variant | G/A;T | snv | 9 |