Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1557570794 | 0.742 | 0.120 | 1 | 26697152 | frameshift variant | -/GCCGCCTCCCTCCTCCAGCGCC | delins | 15 | |||
rs1135401744 | 0.776 | 0.120 | 2 | 142918608 | splice acceptor variant | G/T | snv | 1.4E-04 | 14 | ||
rs869025222 | 0.827 | 0.240 | 3 | 25580574 | missense variant | T/C | snv | 9 | |||
rs28936670 | 0.708 | 0.280 | 5 | 173235011 | missense variant | G/A | snv | 3.4E-03 | 1.1E-02 | 4 | |
rs1232197674 | 0.827 | 0.240 | 6 | 50838070 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 1 | |
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 22 | ||
rs77010898 | 0.742 | 0.280 | 7 | 117642566 | stop gained | G/A;C | snv | 4.6E-04; 4.0E-06 | 4 | ||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 2 | |||
rs1554603293 | 0.752 | 0.320 | 8 | 60849154 | missense variant | G/A | snv | 17 | |||
rs1563595095 | 0.776 | 0.320 | 8 | 60781285 | frameshift variant | AA/T | delins | 10 | |||
rs1554700718 | 0.658 | 0.360 | 9 | 83975540 | non coding transcript exon variant | T/C | snv | 59 | |||
rs121918130 | 0.716 | 0.360 | 9 | 136433182 | missense variant | G/A;T | snv | 3.4E-05; 4.2E-06 | 18 | ||
rs121909224 | 0.627 | 0.560 | 10 | 87933147 | stop gained | C/G;T | snv | 1.2E-05 | 35 | ||
rs121909222 | 0.742 | 0.240 | 10 | 87933127 | missense variant | A/G | snv | 7 | |||
rs387906592 | 0.752 | 0.280 | 10 | 88941309 | missense variant | C/T | snv | 5 | |||
rs1565307564 | 0.807 | 0.120 | 11 | 61783599 | missense variant | A/G | snv | 7 | |||
rs121918459 | 0.662 | 0.440 | 12 | 112450368 | missense variant | A/G | snv | 1.2E-05 | 7.0E-06 | 46 | |
rs121918460 | 0.708 | 0.400 | 12 | 112450364 | missense variant | T/A;G | snv | 4.0E-06 | 27 | ||
rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 19 | ||
rs1057516044 | 0.851 | 0.240 | 12 | 21913005 | missense variant | A/G | snv | 9 | |||
rs587779349 | 0.776 | 0.280 | 13 | 32380040 | frameshift variant | C/- | delins | 8 | |||
rs775394591 | 0.851 | 0.120 | 13 | 38784727 | inframe deletion | TCT/- | delins | 2.8E-05 | 5 | ||
rs200661329 | 0.708 | 0.440 | 16 | 576255 | splice donor variant | G/A;C | snv | 5.7E-05 | 48 | ||
rs1331463984 | 0.701 | 0.240 | 16 | 2176350 | missense variant | G/A | snv | 33 | |||
rs1567744830 | 0.925 | 0.120 | 16 | 70874437 | stop gained | C/A | snv | 3 |