Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs760929207 | 0.925 | 0.200 | 2 | 219568050 | splice donor variant | ACCTTTGACTG/- | delins | 8.1E-06 | 7.0E-06 | 12 | |
rs61753219 | 0.672 | 0.400 | 6 | 42978330 | missense variant | G/A | snv | 3.6E-05 | 2.8E-05 | 64 | |
rs1010184002 | 0.689 | 0.400 | 6 | 42978878 | stop gained | C/T | snv | 7.0E-06 | 60 | ||
rs1561875767 | 1.000 | 0.200 | 6 | 43041036 | stop gained | G/A | snv | 14 | |||
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 | |||
rs1561881909 | 0.925 | 0.200 | 6 | 43044835 | frameshift variant | G/- | delins | 9 | |||
rs1561898352 | 0.882 | 0.200 | 6 | 43052582 | frameshift variant | -/A | delins | 8 | |||
rs1057518871 | 0.925 | 0.120 | 9 | 134798410 | frameshift variant | C/- | delins | 10 | |||
rs863225045 | 0.790 | 0.360 | 10 | 95637327 | missense variant | C/A;T | snv | 15 | |||
rs1232880706 | 0.689 | 0.440 | 15 | 48526247 | stop gained | C/A;T | snv | 36 | |||
rs139751598 | 0.851 | 0.240 | 17 | 81934931 | missense variant | C/T | snv | 2.4E-05 | 4.2E-05 | 13 |