Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs16917234 | 0.925 | 0.080 | 11 | 27676827 | intron variant | T/A;C | snv | 2 | |||
rs16917204 | 0.827 | 0.160 | 11 | 27646808 | intron variant | G/C | snv | 0.17 | 5 | ||
rs2030324 | 0.827 | 0.120 | 11 | 27705368 | intron variant | A/G | snv | 0.49 | 6 | ||
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 |