Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 13 | |
rs1893217 | 0.742 | 0.440 | 18 | 12809341 | intron variant | A/G | snv | 0.12 | 8 | ||
rs13003464 | 0.827 | 0.200 | 2 | 60959694 | intron variant | A/G | snv | 0.50 | 7 | ||
rs212388 | 0.827 | 0.240 | 6 | 159069404 | intron variant | C/G;T | snv | 4 | |||
rs657555 | 0.925 | 0.080 | 18 | 12847137 | intron variant | C/A;T | snv | 3 |