Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs730882249 | 0.882 | 0.120 | 7 | 100105981 | stop gained | C/T | snv | 4.0E-06 | 6 | ||
rs1064796765 | 0.763 | 0.240 | 14 | 102002950 | missense variant | G/A | snv | 19 | |||
rs1057518961 | 0.925 | 0.040 | 14 | 102012450 | missense variant | C/T | snv | 5 | |||
rs1060499740 | 14 | 102348559 | stop lost | A/C | snv | 3 | |||||
rs606231450 | 0.882 | 0.160 | 14 | 105226674 | missense variant | G/C;T | snv | 4.0E-06; 4.0E-06 | 7 | ||
rs373957300 | 0.882 | 0.160 | 14 | 105228832 | missense variant | G/A | snv | 1.6E-05 | 2.8E-05 | 7 | |
rs606231416 | 0.882 | 0.160 | 14 | 105241282 | missense variant | G/A | snv | 8.1E-06 | 7 | ||
rs370270828 | 0.882 | 0.160 | 14 | 105241292 | missense variant | G/A | snv | 8.0E-06 | 2.8E-05 | 7 | |
rs1569508922 | 0.882 | 0.160 | X | 111681268 | missense variant | T/A | snv | 5 | |||
rs369634007 | 0.882 | 0.080 | 2 | 112098688 | missense variant | A/G | snv | 1.6E-05 | 2.1E-05 | 10 | |
rs397507520 | 0.658 | 0.520 | 12 | 112453279 | missense variant | G/C;T | snv | 34 | |||
rs397507531 | 0.752 | 0.320 | 12 | 112473040 | missense variant | T/C;G | snv | 18 | |||
rs587779388 | 1.000 | 1 | 113898755 | frameshift variant | GT/- | delins | 1.4E-04 | 1.5E-04 | 5 | ||
rs869312707 | 0.925 | 0.160 | 12 | 115963422 | missense variant | G/A | snv | 4 | |||
rs1563686762 | 0.790 | 0.280 | 8 | 116847620 | inframe deletion | GTT/- | delins | 16 | |||
rs34757931 | 0.742 | 0.360 | 11 | 119081189 | missense variant | T/G | snv | 1.2E-04 | 5.6E-05 | 26 | |
rs879255522 | 0.925 | 0.120 | 12 | 119822819 | splice donor variant | C/T | snv | 3 | |||
rs879255524 | 1.000 | 0.120 | 12 | 119850217 | missense variant | G/C | snv | 2 | |||
rs879255523 | 1.000 | 0.120 | 12 | 119857525 | stop gained | G/A | snv | 7.0E-06 | 2 | ||
rs119103263 | 0.827 | 0.240 | 1 | 11992659 | missense variant | C/T | snv | 17 | |||
rs782304760 | 0.925 | 0.080 | 12 | 121442391 | missense variant | C/T | snv | 2.8E-05 | 7.0E-06 | 4 | |
rs559979281 | 0.742 | 0.440 | 2 | 121530892 | non coding transcript exon variant | C/G;T | snv | 7.7E-06; 2.3E-05; 3.5E-04 | 23 | ||
rs863225422 | 0.742 | 0.440 | 2 | 121530927 | non coding transcript exon variant | G/A | snv | 4.6E-05; 7.7E-06 | 4.9E-05 | 23 | |
rs796052243 | 0.695 | 0.520 | 4 | 122934574 | inframe deletion | CAA/- | delins | 54 | |||
rs1555155556 | 0.851 | 0.120 | 12 | 12435627 | splice acceptor variant | G/T | snv | 6 |