Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1034395178 | 0.716 | 0.480 | 22 | 20996071 | stop gained | C/A;T | snv | 4.0E-06; 8.0E-06 | 33 | ||
rs1048764460 | 1.000 | 0.040 | 16 | 70482809 | stop gained | C/A | snv | 5.6E-05 | 1 | ||
rs1057518940 | 0.925 | 0.040 | 19 | 38499718 | missense variant | G/A | snv | 4 | |||
rs1057518950 | 0.851 | 0.280 | 2 | 1484815 | missense variant | C/T | snv | 7 | |||
rs1057518961 | 0.925 | 0.040 | 14 | 102012450 | missense variant | C/T | snv | 5 | |||
rs1057518963 | 0.851 | 0.200 | X | 68210239 | missense variant | A/G | snv | 6 | |||
rs1057518966 | 1.000 | 0.040 | 9 | 110800743 | missense variant | G/A | snv | 4 | |||
rs1057519429 | 0.807 | 0.240 | 19 | 13235666 | missense variant | C/G;T | snv | 15 | |||
rs1057521721 | 0.851 | 0.200 | X | 123428020 | missense variant | G/A | snv | 5 | |||
rs121908557 | 0.752 | 0.280 | 17 | 63957514 | missense variant | C/T | snv | 8.2E-06 | 1.4E-05 | 23 | |
rs121909218 | 0.672 | 0.360 | 10 | 87933145 | missense variant | G/A | snv | 25 | |||
rs1287121256 | 0.882 | 0.040 | 5 | 150256777 | missense variant | C/G;T | snv | 7.0E-06 | 9 | ||
rs1400419650 | 0.708 | 0.320 | 14 | 92005938 | stop gained | C/A;T | snv | 4.0E-06 | 1.4E-05 | 38 | |
rs142239530 | 0.790 | 0.320 | 11 | 4091328 | missense variant | C/G;T | snv | 4.4E-05 | 24 | ||
rs1554121872 | 0.882 | 0.040 | 5 | 150250270 | missense variant | T/G | snv | 7 | |||
rs1554121875 | 0.882 | 0.040 | 5 | 150250281 | missense variant | T/C | snv | 7 | |||
rs1554122123 | 0.925 | 0.040 | 5 | 150251979 | splice donor variant | -/A | delins | 5 | |||
rs1554122129 | 0.882 | 0.040 | 5 | 150252032 | missense variant | T/A | snv | 6 | |||
rs1554122526 | 0.882 | 0.040 | 5 | 150256811 | missense variant | A/G | snv | 9 | |||
rs1554123982 | 0.925 | 0.040 | 5 | 150273157 | splice acceptor variant | C/- | delins | 7 | |||
rs1554385305 | 0.925 | 0.040 | 7 | 44241784 | splice acceptor variant | C/T | snv | 7 | |||
rs1554386687 | 0.882 | 0.040 | 7 | 44242328 | missense variant | C/T | snv | 12 | |||
rs1554389088 | 0.807 | 0.160 | 7 | 44243526 | missense variant | G/A | snv | 27 | |||
rs1554893835 | 0.827 | 0.240 | 10 | 87894110 | splice donor variant | G/C;T | snv | 8 | |||
rs1554904159 | 0.851 | 0.160 | 11 | 1442607 | splice donor variant | G/A | snv | 11 |