Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1126671 | 0.851 | 0.120 | 4 | 99127263 | missense variant | T/C | snv | 0.76 | 0.75 | 5 | |
rs1800759 | 0.925 | 0.120 | 4 | 99144358 | intron variant | T/G | snv | 0.49 | 4 | ||
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 83 | ||
rs3735451 | 7 | 99758352 | intron variant | T/C | snv | 0.31 | 1 | ||||
rs4646440 | 7 | 99763247 | intron variant | G/A | snv | 5.1E-02 | 2 | ||||
rs4646437 | 0.827 | 0.200 | 7 | 99767460 | intron variant | G/A | snv | 0.30 | 8 |