Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs441 | 0.882 | 0.200 | 12 | 111791045 | intron variant | T/C | snv | 0.18 | 4 | ||
rs1650420 | 1.000 | 0.080 | 16 | 10174473 | intron variant | T/C | snv | 0.58 | 2 | ||
rs3735451 | 7 | 99758352 | intron variant | T/C | snv | 0.31 | 1 | ||||
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 83 | ||
rs13438494 | 1.000 | 0.040 | 7 | 82759398 | intron variant | T/G | snv | 0.61 | 6 | ||
rs1800759 | 0.925 | 0.120 | 4 | 99144358 | intron variant | T/G | snv | 0.49 | 4 |