Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104894080 | 0.790 | 0.120 | 8 | 74364005 | missense variant | C/T | snv | 3.2E-05 | 4.2E-05 | 9 | |
rs774843232 | 0.851 | 0.080 | 11 | 3825024 | missense variant | G/A;C;T | snv | 8.0E-06; 3.6E-05; 1.2E-05 | 9 | ||
rs139073416 | 0.882 | 0.240 | 1 | 26795056 | missense variant | C/A;T | snv | 1.2E-04 | 9 | ||
rs875989883 | 0.851 | 0.280 | X | 22219070 | missense variant | G/A;C | snv | 9 | |||
rs1567705064 | 1.000 | 0.080 | 17 | 42907570 | frameshift variant | ATGGTCACATCTA/- | del | 8 | |||
rs748219743 | 1.000 | 0.080 | 2 | 233760634 | frameshift variant | -/A | delins | 4 |