Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs797045412 | 0.776 | 0.280 | 9 | 92718565 | missense variant | G/A;T | snv | 17 | |||
rs1561273261 | 0.790 | 0.160 | 5 | 62361307 | missense variant | G/A | snv | 17 | |||
rs776679653 | 0.827 | 0.200 | 9 | 86266174 | missense variant | C/T | snv | 4.2E-06 | 11 | ||
rs386834034 | 0.790 | 0.240 | 1 | 46194853 | stop gained | G/A;T | snv | 2.0E-05 | 9 | ||
rs1567815105 | 0.807 | 0.240 | 16 | 57660794 | frameshift variant | -/T | delins | 7 | |||
rs199422173 | 0.827 | 0.120 | 1 | 197101468 | frameshift variant | CT/- | delins | 2.3E-04 | 1.7E-04 | 7 | |
rs864309676 | 0.851 | 0.120 | 6 | 132472372 | missense variant | T/G | snv | 7 | |||
rs180758272 | 0.882 | 0.080 | 15 | 89649809 | missense variant | C/T | snv | 1.1E-04 | 5.2E-04 | 3 |