Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2854744 | 0.695 | 0.520 | 7 | 45921476 | intron variant | G/T | snv | 0.48 | 20 | ||
rs2854746 | 0.752 | 0.200 | 7 | 45921046 | missense variant | G/A;C;T | snv | 0.38 | 14 | ||
rs3110697 | 0.827 | 0.160 | 7 | 45915430 | intron variant | A/G | snv | 0.58 | 7 | ||
rs538312081 | 1.000 | 0.080 | 7 | 45914942 | missense variant | G/A;C | snv | 1.6E-05 | 1 |