Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057516030 | 0.807 | 0.280 | 21 | 37480785 | stop gained | -/A | delins | 14 | |||
rs1057518934 | 0.851 | 0.240 | 15 | 28211095 | frameshift variant | G/- | delins | 8 | |||
rs1057518963 | 0.851 | 0.200 | X | 68210239 | missense variant | A/G | snv | 6 | |||
rs1057519439 | 1.000 | 0.120 | 2 | 195787135 | missense variant | A/G | snv | 5 | |||
rs1114167295 | 0.827 | 0.160 | X | 54812169 | frameshift variant | C/- | del | 6 | |||
rs1114167296 | 0.827 | 0.160 | X | 34656995 | missense variant | C/G | snv | 6 | |||
rs1114167297 | 0.851 | 0.160 | 10 | 32019912 | missense variant | T/C | snv | 5 | |||
rs1114167298 | 0.882 | 0.120 | 3 | 6861849 | missense variant | T/C | snv | 7.0E-06 | 5 | ||
rs1131692230 | 0.807 | 0.160 | X | 19353124 | missense variant | A/G | snv | 9 | |||
rs114925667 | 0.672 | 0.520 | 3 | 132675903 | missense variant | G/A;T | snv | 1.9E-03; 4.1E-06 | 62 | ||
rs1172486173 | 0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 | 11 | ||
rs1223073957 | 0.827 | 0.240 | 19 | 49835897 | frameshift variant | C/- | delins | 1.2E-05 | 1.4E-05 | 12 | |
rs142239530 | 0.790 | 0.320 | 11 | 4091328 | missense variant | C/G;T | snv | 4.4E-05 | 24 | ||
rs146539065 | 0.752 | 0.240 | 4 | 25145092 | synonymous variant | C/T | snv | 2.8E-05 | 4.2E-05 | 34 | |
rs1553212868 | 0.807 | 0.280 | 1 | 151406264 | frameshift variant | G/- | delins | 17 | |||
rs1553770577 | 0.724 | 0.480 | 3 | 132675342 | missense variant | T/C | snv | 37 | |||
rs1554603293 | 0.752 | 0.320 | 8 | 60849154 | missense variant | G/A | snv | 17 | |||
rs1555038029 | 0.776 | 0.400 | 11 | 118477973 | stop gained | C/A | snv | 12 | |||
rs1555454508 | 0.790 | 0.240 | 15 | 44615487 | stop gained | GTA/ATC | mnv | 18 | |||
rs1555493029 | 0.851 | 0.240 | 16 | 23406263 | splice acceptor variant | C/A | snv | 10 | |||
rs1555497604 | 0.851 | 0.240 | 16 | 23452993 | start lost | A/G | snv | 10 | |||
rs1555954284 | 0.752 | 0.360 | X | 41346607 | missense variant | C/T | snv | 24 | |||
rs1557612048 | 0.807 | 0.200 | 1 | 26767868 | missense variant | T/C | snv | 11 | |||
rs1559307932 | 0.807 | 0.360 | 2 | 231737190 | frameshift variant | -/C | ins | 8 | |||
rs1560755661 | 0.701 | 0.480 | 4 | 106171094 | splice donor variant | CAGATCTGTCTTTGGAGGATCTGGACACTCAGCAGAGAAATAAGGTGCCGAACTTCTGCCTCCACTGCTGTCAGAAGATGGCTTTGGAGGTTGAGCATGCTGTCTGTAAGTAGCACTTTTAGGAGTCCAACAAAACAGGTTGATAGATTCTCTCACACAGCGTTCAATGTCAATTTC/- | delins | 44 |