Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3791679 | 0.925 | 0.120 | 2 | 55869757 | intron variant | A/G | snv | 0.20 | 8 | ||
rs34811474 | 1.000 | 0.040 | 4 | 25407216 | missense variant | G/A;T | snv | 0.15; 4.1E-06 | 8 | ||
rs4252548 | 1.000 | 0.040 | 19 | 55368304 | missense variant | C/T | snv | 2.1E-02 | 1.8E-02 | 3 | |
rs4337252 | 1.000 | 0.040 | 15 | 73934424 | intron variant | G/C | snv | 0.52 | 2 |