Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6314 | 0.677 | 0.360 | 13 | 46834899 | missense variant | G/A | snv | 7.9E-02 | 9.5E-02 | 23 | |
rs150840924 | 0.807 | 0.240 | 1 | 156136359 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 7 | |
rs35677470 | 0.807 | 0.160 | 3 | 58197909 | missense variant | G/A;C | snv | 4.8E-02; 4.0E-06 | 6 | ||
rs3131917 | 0.882 | 0.080 | 5 | 173230018 | upstream gene variant | T/G | snv | 0.52 | 3 | ||
rs7574685 | 0.925 | 0.040 | 2 | 234702877 | intron variant | T/C | snv | 0.59 | 2 |