Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2280401 | 19 | 49496752 | intron variant | G/A | snv | 0.12 | 3 | ||||
rs11078597 | 17 | 1715069 | intron variant | T/C | snv | 0.19 | 2 | ||||
rs11671010 | 19 | 35068570 | intron variant | T/C | snv | 0.11 | 2 | ||||
rs16948098 | 15 | 43927409 | intron variant | G/A | snv | 9.5E-02 | 2 | ||||
rs2293579 | 11 | 47419207 | intron variant | G/A | snv | 0.35 | 0.30 | 2 | |||
rs4806073 | 19 | 35064286 | intron variant | T/C | snv | 0.85 | 2 | ||||
rs694419 | 18 | 62458879 | regulatory region variant | T/C | snv | 0.53 | 2 | ||||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 25 | |
rs12914385 | 0.790 | 0.160 | 15 | 78606381 | intron variant | C/A;T | snv | 8 |