Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 38 | ||
rs4420638 | 0.708 | 0.520 | 19 | 44919689 | downstream gene variant | A/G | snv | 0.18 | 36 | ||
rs5744680 | 0.851 | 0.120 | 5 | 75584065 | intron variant | G/A | snv | 0.55 | 18 | ||
rs1558902 | 0.827 | 0.120 | 16 | 53769662 | intron variant | T/A | snv | 0.31 | 14 | ||
rs2954021 | 1.000 | 0.040 | 8 | 125469835 | intron variant | A/G | snv | 0.54 | 14 | ||
rs715 | 1.000 | 0.040 | 2 | 210678331 | 3 prime UTR variant | T/C | snv | 0.28 | 12 | ||
rs1126930 | 12 | 49005349 | missense variant | G/C | snv | 2.1E-02 | 2.1E-02 | 5 | |||
rs36023504 | 4 | 38697303 | 3 prime UTR variant | C/G;T | snv | 0.24 | 0.24 | 3 | |||
rs7185966 | 16 | 3972702 | intron variant | G/A | snv | 0.26 | 3 |