Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs387907145 | 0.695 | 0.440 | 16 | 4800548 | stop gained | G/A | snv | 36 | |||
rs786205124 | 0.701 | 0.400 | 16 | 4798593 | frameshift variant | G/-;GGG | delins | 3.5E-05 | 35 | ||
rs121913485 | 0.716 | 0.400 | 4 | 1804372 | missense variant | A/G | snv | 18 | |||
rs121913478 | 0.708 | 0.640 | 10 | 121515280 | missense variant | T/C | snv | 17 | |||
rs1057516030 | 0.807 | 0.280 | 21 | 37480785 | stop gained | -/A | delins | 14 | |||
rs886039795 | 0.851 | 0.160 | 17 | 7403143 | frameshift variant | CACTCAGAGCCTGGTAGTAAAA/- | del | 10 | |||
rs780261665 | 0.827 | 0.200 | 3 | 48590258 | stop gained | G/A | snv | 2.0E-05 | 1.4E-05 | 9 | |
rs557849165 | 0.776 | 0.160 | 17 | 10656089 | splice donor variant | C/T | snv | 1.2E-03 | 9 | ||
rs767978562 | 0.790 | 0.320 | 13 | 38851093 | stop gained | C/T | snv | 8.0E-06 | 7.0E-06 | 8 | |
rs1057518960 | 0.882 | 0.160 | 6 | 121447333 | missense variant | G/C | snv | 7 | |||
rs1567552713 | 0.827 | 0.120 | 17 | 10633590 | splice donor variant | C/T | snv | 7 | |||
rs1057518863 | 0.925 | 0.120 | 3 | 48567190 | missense variant | C/A;T | snv | 4 |