Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs137852865 | 1.000 | 0.120 | 12 | 121849726 | missense variant | T/C | snv | 3.2E-05 | 7.0E-06 | 1 | |
rs137852866 | 1.000 | 0.120 | 12 | 121846919 | stop gained | A/C | snv | 1 | |||
rs137852867 | 1.000 | 0.120 | 12 | 121847211 | stop gained | G/C | snv | 4.0E-06 | 1 | ||
rs367674632 | 0.925 | 0.120 | 12 | 121857775 | stop gained | C/G;T | snv | 5.2E-05 | 1.4E-05 | 2 | |
rs775747384 | 0.925 | 0.120 | 12 | 121857807 | stop gained | G/A | snv | 8.0E-06 | 7.0E-06 | 2 |