Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1553920379 | 0.776 | 0.160 | 4 | 101032294 | frameshift variant | -/AGTA | delins | 27 | |||
rs1043614377 | 1.000 | 0.040 | 10 | 103049727 | missense variant | G/A | snv | 2 | |||
rs1562159088 | 1.000 | 0.040 | 6 | 110100644 | stop gained | G/A | snv | 2 | |||
rs786205232 | 0.925 | 0.040 | 1 | 110603893 | missense variant | C/T | snv | 4.0E-06 | 5 | ||
rs886041874 | 1.000 | 0.040 | 1 | 119721323 | splice donor variant | T/C | snv | 4.0E-06 | 2 | ||
rs764618040 | 1.000 | 0.040 | 1 | 119726868 | missense variant | C/T | snv | 1.6E-05 | 2.1E-05 | 2 | |
rs587776508 | 0.882 | 0.040 | 12 | 123253922 | frameshift variant | T/- | del | 4.0E-06 | 4 | ||
rs1057519538 | 1.000 | 0.040 | 9 | 127651622 | inframe deletion | AAA/- | del | 1 | |||
rs1057518985 | 1.000 | 0.040 | 9 | 127673233 | missense variant | C/A;T | snv | 1 | |||
rs796053366 | 0.925 | 0.040 | 9 | 127673250 | stop gained | C/T | snv | 2 | |||
rs796053367 | 0.925 | 0.040 | 9 | 127675909 | missense variant | C/T | snv | 2 | |||
rs1057519539 | 1.000 | 0.040 | 9 | 127678479 | stop gained | G/A;T | snv | 1 | |||
rs1057519537 | 1.000 | 0.040 | 9 | 127682423 | stop gained | G/A | snv | 1 | |||
rs869312702 | 0.827 | 0.160 | 9 | 128203609 | missense variant | G/A | snv | 10 | |||
rs796053335 | 1.000 | 0.040 | 9 | 128632280 | protein altering variant | -/GCATGC | delins | 1 | |||
rs121909323 | 0.790 | 0.160 | 19 | 13277122 | stop gained | G/A | snv | 8 | |||
rs786200962 | 0.827 | 0.120 | 19 | 13298768 | frameshift variant | A/- | del | 7 | |||
rs1064794262 | 0.925 | 0.040 | 19 | 13303831 | frameshift variant | CT/- | del | 3 | |||
rs28934908 | 0.732 | 0.280 | X | 154031409 | missense variant | G/A;T | snv | 5.5E-06 | 23 | ||
rs587777308 | 0.763 | 0.040 | 5 | 161873196 | missense variant | G/A | snv | 14 | |||
rs727503940 | 1.000 | 0.040 | 5 | 161882638 | missense variant | C/A;T | snv | 1 | |||
rs796052491 | 0.851 | 0.040 | 5 | 161890982 | missense variant | T/A;C | snv | 4 | |||
rs1060499553 | 0.827 | 0.040 | 5 | 161890983 | missense variant | G/A | snv | 6 | |||
rs796052493 | 0.851 | 0.040 | 5 | 161895668 | missense variant | G/A;T | snv | 4 | |||
rs747138999 | 1.000 | 0.040 | 5 | 161895753 | missense variant | G/T | snv | 2 |