Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11887534 | 0.653 | 0.440 | 2 | 43839108 | missense variant | G/A;C | snv | 6.4E-06; 6.7E-02 | 29 | ||
rs2287622 | 0.724 | 0.240 | 2 | 168973818 | missense variant | A/C;G;T | snv | 0.57 | 16 | ||
rs4148217 | 0.790 | 0.280 | 2 | 43872294 | missense variant | C/A;T | snv | 0.21; 1.2E-05 | 11 | ||
rs2230028 | 0.827 | 0.080 | 7 | 87426860 | missense variant | T/C;G | snv | 1.0E-01 | 5 | ||
rs1382897404 | 0.851 | 0.040 | 2 | 169018071 | missense variant | C/G | snv | 7.0E-06 | 4 | ||
rs58238559 | 0.882 | 0.120 | 7 | 87452957 | missense variant | T/C | snv | 1.1E-02 | 9.2E-03 | 3 | |
rs767587977 | 0.882 | 0.120 | 2 | 21002962 | stop gained | C/A;T | snv | 8.2E-06 | 3 | ||
rs1478060232 | 0.925 | 0.040 | 2 | 168969407 | missense variant | T/C | snv | 2 | |||
rs747471233 | 0.925 | 0.040 | 2 | 169018074 | missense variant | C/G | snv | 4.0E-06 | 2 | ||
rs769652427 | 0.925 | 0.040 | 2 | 168971917 | missense variant | G/C | snv | 1.2E-05 | 2 | ||
rs1205128669 | 0.925 | 0.040 | 2 | 43877848 | missense variant | G/A;C | snv | 4.0E-06 | 2 | ||
rs755130225 | 0.925 | 0.040 | 2 | 43877845 | missense variant | G/A | snv | 8.0E-06 | 2 |