Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1561875767 | 1.000 | 0.200 | 6 | 43041036 | stop gained | G/A | snv | 14 | |||
rs139751598 | 0.851 | 0.240 | 17 | 81934931 | missense variant | C/T | snv | 2.4E-05 | 4.2E-05 | 13 | |
rs1561892336 | 0.807 | 0.200 | 6 | 43050050 | stop gained | C/T | snv | 13 | |||
rs1561873941 | 0.925 | 0.200 | 6 | 43040335 | frameshift variant | T/- | del | 10 | |||
rs1561898352 | 0.882 | 0.200 | 6 | 43052582 | frameshift variant | -/A | delins | 8 |