Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121912438 | 0.605 | 0.520 | 21 | 31667299 | missense variant | G/A;C;T | snv | 1.2E-05; 8.0E-06 | 58 | ||
rs1475170339 | 0.732 | 0.240 | 16 | 1792325 | missense variant | T/C;G | snv | 18 | |||
rs121964856 | 0.807 | 0.120 | 1 | 201365297 | missense variant | C/A;T | snv | 8 | |||
rs57965306 | 0.925 | 0.160 | 2 | 219421365 | missense variant | G/A;C | snv | 2.8E-05 | 6 | ||
rs746686166 | 0.925 | 0.280 | 2 | 97646179 | missense variant | G/A;T | snv | 6.7E-06 | 4 | ||
rs201078173 | 0.925 | 0.280 | 12 | 113399616 | missense variant | C/T | snv | 8.6E-06 | 7.0E-05 | 4 |