Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397508118 | 0.851 | 0.120 | 11 | 2570720 | frameshift variant | GCGCT/- | delins | 1.4E-05 | 4 | ||
rs397508120 | 0.882 | 0.120 | 11 | 2570734 | frameshift variant | G/- | delins | 3 | |||
rs199472755 | 0.851 | 0.120 | 11 | 2583478 | missense variant | C/A;G;T | snv | 4.0E-06 | 4 | ||
rs1167115018 | 0.827 | 0.160 | 6 | 26092760 | missense variant | A/G | snv | 8.0E-06 | 7.0E-06 | 5 | |
rs151344631 | 0.827 | 0.200 | 11 | 2571333 | missense variant | G/A | snv | 8.0E-06 | 3.5E-05 | 5 | |
rs199472702 | 0.882 | 0.120 | 11 | 2570754 | missense variant | G/A;C | snv | 8.1E-06 | 3 | ||
rs74315446 | 0.851 | 0.120 | 21 | 34449414 | missense variant | G/A;C | snv | 1.6E-05 | 4 | ||
rs199472815 | 0.851 | 0.120 | 11 | 2778024 | missense variant | G/A;C | snv | 2.0E-05 | 4 | ||
rs74315445 | 0.807 | 0.120 | 21 | 34449409 | missense variant | C/T | snv | 6.8E-05 | 5.3E-05 | 6 | |
rs17215500 | 0.807 | 0.240 | 11 | 2768881 | stop gained | C/G;T | snv | 1.0E-04 | 7 |