Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs369158322 | 1.000 | 0.080 | 8 | 31150454 | missense variant | A/C;T | snv | 4.0E-06 | 1 | ||
rs371538747 | 1.000 | 0.080 | 8 | 31064406 | stop gained | T/A;C;G | snv | 4.0E-06 | 1 | ||
rs121908447 | 1.000 | 0.080 | 8 | 31147397 | stop gained | C/T | snv | 1 | |||
rs121908448 | 1.000 | 0.080 | 8 | 31090843 | missense variant | A/T | snv | 1 | |||
rs1303126572 | 1.000 | 0.080 | 8 | 31157509 | stop gained | C/T | snv | 7.0E-06 | 1 | ||
rs1304645785 | 1.000 | 0.080 | 8 | 31090532 | missense variant | G/A | snv | 1 | |||
rs1361270203 | 1.000 | 0.080 | 8 | 31067049 | frameshift variant | -/CT | delins | 1 | |||
rs1554519254 | 1.000 | 0.080 | 8 | 31067035 | frameshift variant | -/AA | delins | 1 | |||
rs1554519449 | 1.000 | 0.080 | 8 | 31068326 | splice donor variant | GGTA/- | delins | 1 | |||
rs1554526707 | 1.000 | 0.080 | 8 | 31111632 | frameshift variant | -/A | delins | 1 | |||
rs1554527775 | 1.000 | 0.080 | 8 | 31116412 | stop gained | C/T | snv | 1 | |||
rs1554528411 | 1.000 | 0.080 | 8 | 31120398 | stop gained | G/A | snv | 1 | |||
rs1563331288 | 1.000 | 0.080 | 8 | 31067082 | stop gained | T/G | snv | 1 | |||
rs1563338837 | 1.000 | 0.080 | 8 | 31081138 | stop gained | G/T | snv | 1 | |||
rs1563338855 | 1.000 | 0.080 | 8 | 31081141 | frameshift variant | GA/C | delins | 1 | |||
rs1563341296 | 1.000 | 0.080 | 8 | 31085164 | splice acceptor variant | A/G | snv | 1 | |||
rs1563357741 | 1.000 | 0.080 | 8 | 31111696 | stop gained | C/T | snv | 1 | |||
rs1563376347 | 1.000 | 0.080 | 8 | 31141456 | stop gained | T/A | snv | 1 | |||
rs1563376526 | 1.000 | 0.080 | 8 | 31141564 | stop gained | T/G | snv | 1 | |||
rs1563376793 | 1.000 | 0.080 | 8 | 31141776 | splice donor variant | G/C | snv | 1 | |||
rs1563382597 | 1.000 | 0.080 | 8 | 31150450 | frameshift variant | G/- | del | 1 | |||
rs1563385391 | 1.000 | 0.080 | 8 | 31154644 | frameshift variant | A/- | delins | 1 | |||
rs267607008 | 1.000 | 0.080 | 8 | 31064962 | missense variant | A/G | snv | 1 | |||
rs281865157 | 1.000 | 0.080 | 8 | 31108591 | intron variant | A/C;G | snv | 1 | |||
rs281865158 | 1.000 | 0.080 | 8 | 31111704 | frameshift variant | -/T | delins | 1 |