Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121908950 | 1.000 | 0.120 | 10 | 87743589 | stop gained | C/A | snv | 1 | |||
rs121908951 | 1.000 | 0.120 | 10 | 87709311 | missense variant | C/G | snv | 1 | |||
rs1471554906 | 1.000 | 0.120 | 10 | 87715027 | frameshift variant | TT/- | delins | 1 | |||
rs606231241 | 1.000 | 0.120 | 10 | 87713265 | frameshift variant | -/G | delins | 1 | |||
rs606231242 | 1.000 | 0.120 | 10 | 87714838 | frameshift variant | GTAGTGGAACTTCTGCAAG/- | delins | 1 | |||
rs606231243 | 1.000 | 0.120 | 10 | 87714137 | frameshift variant | -/CGTA | delins | 1 | |||
rs786200933 | 1.000 | 0.120 | 10 | 87743455 | frameshift variant | AG/- | delins | 1 | |||
rs786200934 | 1.000 | 0.120 | 10 | 87715005 | frameshift variant | A/- | delins | 1 | |||
rs797045099 | 1.000 | 0.120 | 10 | 87745166 | frameshift variant | ATTCC/- | delins | 1 | |||
rs121908952 | 1.000 | 0.120 | 10 | 87727403 | stop gained | C/T | snv | 3.6E-05 | 1.4E-05 | 1 |