Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1554777480 | 9 | 127666235 | missense variant | C/G | snv | 2 | |||||
rs1553510217 | 1.000 | 0.040 | 2 | 161417083 | missense variant | A/T | snv | 2 | |||
rs1553510301 | 0.925 | 0.040 | 2 | 161417794 | missense variant | T/C | snv | 2 | |||
rs1553511216 | 1.000 | 0.040 | 2 | 161423815 | frameshift variant | -/GCCCGCAGTC | delins | 2 | |||
rs1553511226 | 1.000 | 0.040 | 2 | 161423830 | frameshift variant | GC/- | delins | 2 | |||
rs730882243 | 1.000 | 0.120 | 1 | 215602099 | frameshift variant | CCCTTGCGAATGAAAGATAATGATCTTCTTGTAACTGA/- | del | 3 | |||
rs1057518928 | 1.000 | 0.040 | 12 | 23665471 | missense variant | G/A | snv | 3 | |||
rs756210458 | 0.925 | 0.200 | 22 | 40354266 | missense variant | C/G;T | snv | 4.0E-06; 1.2E-05 | 4 | ||
rs74315511 | 0.925 | 0.240 | 22 | 50523994 | missense variant | C/T | snv | 8.0E-05 | 1.1E-04 | 4 | |
rs121434578 | 1.000 | 0.080 | 16 | 8768248 | missense variant | G/A | snv | 5 | |||
rs724159990 | 1.000 | 0.080 | 16 | 8768220 | missense variant | C/T | snv | 5 | |||
rs724159992 | 1.000 | 0.080 | 16 | 8750498 | missense variant | G/A | snv | 1.4E-05 | 5 | ||
rs374259530 | 0.925 | 0.200 | 22 | 40350018 | missense variant | T/C | snv | 3.6E-05 | 9.1E-05 | 5 | |
rs869025221 | 0.925 | 0.080 | 3 | 25593603 | missense variant | G/C | snv | 5 | |||
rs724159991 | 1.000 | 0.080 | 16 | 8781360 | missense variant | T/C | snv | 5 | |||
rs375761808 | 0.925 | 0.160 | 1 | 26775673 | missense variant | A/G;T | snv | 4.0E-06 | 6 | ||
rs1057518887 | 0.925 | 0.160 | 4 | 25156851 | splice region variant | C/T | snv | 7 | |||
rs61749715 | 0.851 | 0.120 | X | 154031154 | missense variant | G/A;C | snv | 8 | |||
rs372392424 | 0.882 | 0.240 | 4 | 523849 | missense variant | C/T | snv | 6.7E-05 | 7.7E-05 | 8 | |
rs869025222 | 0.827 | 0.240 | 3 | 25580574 | missense variant | T/C | snv | 9 | |||
rs74315442 | 0.851 | 0.200 | 21 | 43774297 | stop gained | G/A | snv | 4.0E-05 | 2.1E-05 | 10 | |
rs776720232 | 0.827 | 0.240 | 17 | 39673099 | missense variant | T/C;G | snv | 4.2E-06 | 10 | ||
rs1553511224 | 0.882 | 0.080 | 2 | 161423825 | frameshift variant | -/C | delins | 10 | |||
rs869312704 | 0.882 | 0.160 | 2 | 161423752 | frameshift variant | -/GGCTGCA | delins | 10 | |||
rs1555652383 | 0.807 | 0.160 | 17 | 67912720 | frameshift variant | TG/- | delins | 13 |