Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs797045969 | 1.000 | 0.040 | 11 | 792722 | stop gained | G/A | snv | 1 | |||
rs587777243 | 1.000 | 0.040 | 11 | 792954 | missense variant | C/G | snv | 1 | |||
rs1565035177 | 0.925 | 0.040 | 11 | 792146 | frameshift variant | CA/- | delins | 4 | |||
rs1554965669 | 0.925 | 0.040 | 11 | 792888 | stop gained | G/A | snv | 2 | |||
rs121918335 | 1.000 | 0.040 | 11 | 792340 | missense variant | C/A | snv | 1 | |||
rs121918334 | 1.000 | 0.040 | 11 | 792429 | missense variant | G/A | snv | 1.2E-05 | 2.8E-05 | 1 | |
rs1195505218 | 0.925 | 0.040 | 11 | 792142 | missense variant | C/T | snv | 4.1E-06 | 4 |