Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13063578 | 3 | 47046347 | intron variant | T/A | snv | 0.46 | 5 | ||||
rs3735485 | 7 | 44969742 | missense variant | A/G | snv | 0.87 | 0.88 | 6 | |||
rs112401631 | 0.882 | 0.120 | 17 | 40608272 | TF binding site variant | T/A | snv | 1.1E-02 | 8 | ||
rs3131643 | 6 | 31475005 | intron variant | G/A | snv | 0.12 | 2 | ||||
rs2524079 | 6 | 31274397 | intron variant | G/A | snv | 0.44 | 6 | ||||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 55 | |
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 34 | |
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 61 | ||
rs36084354 | 19 | 1079960 | missense variant | G/A | snv | 5.7E-02 | 5.9E-02 | 3 |