Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs137854466 | 0.724 | 0.320 | 15 | 48411280 | stop gained | G/A;C | snv | 4.0E-05; 8.0E-06 | 23 | ||
rs587784105 | 0.732 | 0.440 | 5 | 177235863 | stop gained | G/A | snv | 19 | |||
rs112550005 | 0.742 | 0.240 | 15 | 48425829 | stop gained | G/A | snv | 18 | |||
rs1566823361 | 0.742 | 0.440 | 13 | 101726732 | frameshift variant | -/G | delins | 18 | |||
rs111854391 | 0.716 | 0.280 | 9 | 99138006 | stop gained | C/A;T | snv | 4.0E-06 | 18 | ||
rs113422242 | 0.763 | 0.240 | 15 | 48510065 | stop gained | G/A | snv | 7.0E-06 | 14 | ||
rs1555397413 | 0.732 | 0.280 | 15 | 48470705 | missense variant | T/C | snv | 13 | |||
rs142110773 | 0.882 | 0.160 | 7 | 50463317 | missense variant | G/A | snv | 1.6E-05 | 7.0E-06 | 13 | |
rs137854461 | 0.790 | 0.280 | 15 | 48437026 | missense variant | T/C | snv | 12 | |||
rs113812345 | 0.790 | 0.160 | 15 | 48513591 | stop gained | G/A | snv | 10 | |||
rs1555398397 | 0.807 | 0.240 | 15 | 48485436 | missense variant | C/T | snv | 10 | |||
rs397515789 | 0.776 | 0.240 | 15 | 48488112 | splice donor variant | C/A;T | snv | 10 | |||
rs1085308004 | 0.807 | 0.240 | 15 | 48425420 | missense variant | A/G | snv | 9 | |||
rs761857514 | 0.851 | 0.240 | 15 | 48452676 | stop gained | C/A;T | snv | 4.0E-06 | 8 | ||
rs771487311 | 0.882 | 0.120 | 11 | 103255530 | missense variant | T/C | snv | 1.9E-05 | 7.0E-05 | 5 | |
rs759549373 | 0.925 | 0.080 | 11 | 103253342 | missense variant | G/A;T | snv | 6.0E-05; 4.0E-06 | 4 | ||
rs863223722 | 1.000 | 0.160 | 1 | 2229305 | missense variant | C/A;T | snv | 2 |