Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1032242817 | 0.807 | 0.320 | 11 | 71441307 | stop gained | C/T | snv | 8.0E-06 | 7.0E-06 | 17 | |
rs1043679457 | 0.752 | 0.400 | 5 | 60927745 | intron variant | C/A;G;T | snv | 33 | |||
rs1057518921 | 1.000 | X | 71132465 | missense variant | G/A | snv | 7 | ||||
rs1057519389 | 0.695 | 0.400 | 10 | 129957324 | missense variant | C/A;G;T | snv | 46 | |||
rs1085308053 | 0.882 | 0.080 | 10 | 87952230 | missense variant | C/T | snv | 5 | |||
rs121912708 | 1.000 | 0.040 | 5 | 126583997 | stop gained | G/A;C | snv | 6.0E-05; 4.0E-06 | 3 | ||
rs137854889 | 0.742 | 0.440 | 1 | 40290871 | frameshift variant | T/-;TT | delins | 31 | |||
rs138659167 | 0.807 | 0.320 | 11 | 71435840 | splice acceptor variant | C/A;G | snv | 5.6E-05; 3.9E-03 | 20 | ||
rs140845195 | 1.000 | 0.040 | 5 | 126545020 | splice acceptor variant | C/A;T | snv | 1.6E-05; 4.0E-06 | 3 | ||
rs1554333853 | 0.689 | 0.320 | 7 | 40046006 | missense variant | A/G | snv | 54 | |||
rs1554603293 | 0.752 | 0.320 | 8 | 60849154 | missense variant | G/A | snv | 17 | |||
rs1554823375 | 0.851 | 0.160 | 10 | 1080454 | missense variant | C/T | snv | 8 | |||
rs1555640521 | 0.790 | 0.320 | 18 | 6942110 | frameshift variant | A/- | delins | 15 | |||
rs1556425596 | 0.752 | 0.240 | 21 | 45989967 | intron variant | C/T | snv | 37 | |||
rs1559720382 | 1.000 | 3 | 47101476 | missense variant | T/C | snv | 2 | ||||
rs1560755661 | 0.701 | 0.480 | 4 | 106171094 | splice donor variant | CAGATCTGTCTTTGGAGGATCTGGACACTCAGCAGAGAAATAAGGTGCCGAACTTCTGCCTCCACTGCTGTCAGAAGATGGCTTTGGAGGTTGAGCATGCTGTCTGTAAGTAGCACTTTTAGGAGTCCAACAAAACAGGTTGATAGATTCTCTCACACAGCGTTCAATGTCAATTTC/- | delins | 44 | |||
rs1565977796 | 0.882 | 0.120 | 13 | 26337623 | stop gained | C/A | snv | 7 | |||
rs1567053134 | 0.925 | 0.040 | 15 | 74345160 | frameshift variant | AG/- | del | 8 | |||
rs1569234334 | 0.851 | 0.200 | X | 70329420 | missense variant | G/T | snv | 5 | |||
rs1569355102 | 0.695 | 0.360 | 21 | 37472869 | frameshift variant | TAAC/- | delins | 51 | |||
rs267607093 | 0.851 | 0.160 | 4 | 55359444 | stop gained | G/A | snv | 4.0E-06 | 14 | ||
rs397515415 | 0.807 | 0.240 | X | 72495216 | stop gained | G/A;T | snv | 10 | |||
rs431905509 | 0.807 | 0.280 | 22 | 19176222 | missense variant | G/A;C | snv | 2.0E-05 | 8 | ||
rs542652468 | 0.882 | 19 | 41986177 | missense variant | G/A;T | snv | 6 | ||||
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 |