Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1085307993 | 0.716 | 0.440 | 5 | 161331056 | missense variant | C/T | snv | 53 | |||
rs139751598 | 0.851 | 0.240 | 17 | 81934931 | missense variant | C/T | snv | 2.4E-05 | 4.2E-05 | 13 | |
rs147484110 | 0.807 | 0.200 | 21 | 43774760 | splice acceptor variant | C/G | snv | 1.5E-04 | 2.7E-04 | 11 | |
rs1554389088 | 0.807 | 0.160 | 7 | 44243526 | missense variant | G/A | snv | 27 | |||
rs1554863016 | 0.882 | 0.240 | 10 | 92648211 | splice acceptor variant | G/A | snv | 5 | |||
rs1555429629 | 0.763 | 0.200 | 15 | 40729632 | missense variant | G/A | snv | 23 | |||
rs1555740650 | 0.807 | 0.240 | 19 | 49596253 | stop gained | G/T | snv | 13 | |||
rs1569548274 | 0.701 | 0.520 | X | 154030553 | splice acceptor variant | TCCAGTGAGCCTCCTCTGGGCATCTTCTCCTCTTTGCAGACGCTGCTGCTCAAGTCCTGGGGCTCAGGGGGGCTGGTGGGGTCCTCGGAGCTCTCGGGCTCAGGTGGAGGTGGGGGCAGGGGTGGGAGCAGTGGCACGGGGGCCTTTGGGGACTCTGAGTGGTGGTGATGGTGGTGGTGCTCCTTCTTGGGGGGTGAGGAGGCGCTGCTGCTGCGCCCCTTGGGGCTGCTCTCCTTGCTTTTCCGCCCAGGGCTCTTACAGGTCTTCAGTCCTTTCCCGCTCTTCTCACCGAGGGTGGACACCAGCAGGGGCTTCACCACTTCCTTGACCTCGATGCTGACCGTCTCCCGGGTCTTGCGCTTCTTGATGGGGAGTACGGTCTCCTGCACAGATCGGATAGAAGACTCCTTCACGGCTTTCTTTTTGGCCTCGGCGGCAGCGGCTGCCACCACACTCCCCGGCTTTCGGCCCCGTTTCTTGGGAATGGCCTGAGGGTCGGCCTCAGCTTTTCGCTTCCTGCCGGGGCGTTTGATCACCATGACCTGGGTGGATGTGGTGGCCCCACCCCCCTCAGC/- | delins | 43 | |||
rs188675529 | 0.827 | 0.240 | 16 | 67842794 | missense variant | C/G;T | snv | 1.6E-03 | 6.0E-04 | 11 | |
rs28936415 | 0.752 | 0.320 | 16 | 8811153 | missense variant | G/A | snv | 4.1E-03 | 3.7E-03 | 22 | |
rs386834070 | 0.851 | 0.360 | 8 | 99134644 | stop gained | C/T | snv | 9 | |||
rs387906702 | 0.807 | 0.200 | X | 53403635 | missense variant | A/G | snv | 16 | |||
rs531163149 | 1.000 | 16 | 70664131 | missense variant | G/A;C | snv | 1.3E-04; 4.1E-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 | ||
rs587777623 | 0.882 | 0.120 | 11 | 686986 | missense variant | G/A | snv | 4.0E-06 | 5 | ||
rs587779388 | 1.000 | 1 | 113898755 | frameshift variant | GT/- | delins | 1.4E-04 | 1.5E-04 | 5 | ||
rs61749721 | 0.732 | 0.200 | X | 154031065 | stop gained | G/A | snv | 15 | |||
rs61753219 | 0.672 | 0.400 | 6 | 42978330 | missense variant | G/A | snv | 3.6E-05 | 2.8E-05 | 64 | |
rs780533096 | 0.701 | 0.600 | 13 | 23886338 | missense variant | C/G;T | snv | 4.8E-06; 9.6E-06 | 44 | ||
rs782304760 | 0.925 | 0.080 | 12 | 121442391 | missense variant | C/T | snv | 2.8E-05 | 7.0E-06 | 4 | |
rs782596945 | 0.851 | 0.120 | X | 153580229 | missense variant | G/A;T | snv | 5.5E-06 | 8 | ||
rs786200952 | 0.851 | 0.120 | 8 | 41934340 | frameshift variant | -/T | delins | 13 | |||
rs863225045 | 0.790 | 0.360 | 10 | 95637327 | missense variant | C/A;T | snv | 15 | |||
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 | |
rs869312685 | 0.807 | 0.240 | 3 | 4815135 | missense variant | G/A;C | snv | 11 |