Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1554700718 | 0.658 | 0.360 | 9 | 83975540 | non coding transcript exon variant | T/C | snv | 59 | |||
rs796052243 | 0.695 | 0.520 | 4 | 122934574 | inframe deletion | CAA/- | delins | 54 | |||
rs1555038111 | 0.701 | 0.480 | 11 | 118478153 | stop gained | T/G | snv | 37 | |||
rs1554699491 | 0.763 | 0.280 | 9 | 85596450 | splice acceptor variant | C/A | snv | 23 | |||
rs780631499 | 0.763 | 0.280 | 9 | 85588465 | frameshift variant | G/- | del | 4.0E-06 | 7.0E-06 | 23 | |
rs12720458 | 0.716 | 0.240 | 11 | 2585264 | missense variant | A/G | snv | 4.0E-05 | 1.4E-05 | 20 | |
rs1057518879 | 0.776 | 0.280 | 1 | 11965571 | stop gained | G/A | snv | 19 | |||
rs1553212868 | 0.807 | 0.280 | 1 | 151406264 | frameshift variant | G/- | delins | 17 | |||
rs1569301036 | 0.827 | 0.240 | X | 71397354 | missense variant | C/T | snv | 17 | |||
rs587783772 | 0.776 | 0.200 | X | 150659665 | missense variant | G/A;T | snv | 14 | |||
rs1555038029 | 0.776 | 0.400 | 11 | 118477973 | stop gained | C/A | snv | 12 | |||
rs1567263168 | 0.851 | 0.240 | 16 | 3729444 | missense variant | C/T | snv | 10 | |||
rs1057519443 | 0.882 | 0.200 | 2 | 201675255 | missense variant | A/G | snv | 7 |