Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2238731 | 0.882 | 0.120 | 22 | 18918464 | missense variant | C/T | snv | 3.8E-02 | 2 | ||
rs2870983 | 0.882 | 0.120 | 22 | 18918329 | missense variant | C/T | snv | 4.9E-02; 4.0E-06 | 5.5E-02 | 2 | |
rs2904551 | 0.776 | 0.160 | 22 | 18918421 | missense variant | A/G | snv | 5.2E-03 | 2.8E-03 | 2 | |
rs3970559 | 0.851 | 0.120 | 22 | 18918386 | missense variant | G/A | snv | 1.1E-02 | 2 | ||
rs450046 | 0.851 | 0.280 | 22 | 18913491 | missense variant | C/T | snv | 0.93 | 2.8E-03 | 2 | |
rs2870984 | 0.925 | 0.080 | 22 | 18918346 | missense variant | G/A | snv | 4.6E-03 | 3.3E-03 | 1 | |
rs3970555 | 1.000 | 22 | 18919485 | missense variant | G/A | snv | 1.9E-03 | 1.5E-03 | 1 |