Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9282799 | 1.000 | 0.080 | 17 | 27801702 | intron variant | G/A | snv | 1.5E-02 | 1 | ||
rs1333955 | 0.851 | 0.080 | 6 | 162792422 | intron variant | T/A;C | snv | 4 | |||
rs2069705 | 0.695 | 0.440 | 12 | 68161231 | intron variant | G/A;C | snv | 19 | |||
rs17235409 | 0.653 | 0.600 | 2 | 218395009 | missense variant | G/A;C | snv | 4.9E-02; 4.1E-06 | 31 |