Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6025 | 0.637 | 0.560 | 1 | 169549811 | missense variant | C/T | snv | 1.8E-02 | 43 | ||
rs121909607 | 0.882 | 0.160 | 4 | 154589513 | missense variant | C/T | snv | 1.2E-05 | 1.4E-05 | 4 | |
rs121909606 | 0.925 | 0.080 | 4 | 154589514 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 2 | |
rs1276352833 | 0.925 | 0.080 | 4 | 154586057 | missense variant | G/A;T | snv | 4.0E-06; 4.0E-06 | 2 | ||
rs121913087 | 0.925 | 0.080 | 4 | 154606933 | missense variant | G/A | snv | 2 | |||
rs778686781 | 1.000 | 0.080 | 6 | 160718329 | missense variant | T/C | snv | 4.0E-06 | 1 |