Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1060499548 | 0.724 | 0.440 | 9 | 130872961 | missense variant | G/A | snv | 27 | |||
rs1555955296 | 0.742 | 0.320 | X | 18628716 | stop gained | C/T | snv | 17 | |||
rs768663992 | 0.882 | 0.160 | 16 | 3508407 | missense variant | T/G | snv | 1.3E-05 | 4.2E-05 | 5 | |
rs769705065 | 0.882 | 0.160 | 16 | 3520011 | stop gained | C/T | snv | 7.0E-06 | 5 | ||
rs1057524157 | 0.776 | 0.200 | 11 | 686962 | missense variant | A/C;T | snv | 19 | |||
rs11555217 | 0.882 | 0.160 | 11 | 71441401 | stop gained | C/G;T | snv | 7.7E-04 | 5 | ||
rs779896782 | 0.882 | 0.160 | 11 | 71439055 | missense variant | A/C;G | snv | 8.0E-06 | 5 | ||
rs1557036768 | 0.708 | 0.320 | X | 53647390 | missense variant | C/T | snv | 44 | |||
rs1135401744 | 0.776 | 0.120 | 2 | 142918608 | splice acceptor variant | G/T | snv | 1.4E-04 | 14 | ||
rs864309532 | 0.807 | 0.360 | X | 134393952 | missense variant | G/A | snv | 7 | |||
rs368869806 | 0.614 | 0.480 | 9 | 95485875 | splice acceptor variant | C/T | snv | 4.0E-06 | 7.0E-06 | 97 | |
rs1555429629 | 0.763 | 0.200 | 15 | 40729632 | missense variant | G/A | snv | 23 | |||
rs1554504663 | 0.851 | 0.080 | 8 | 23007627 | missense variant | G/A | snv | 11 | |||
rs1057524820 | 0.776 | 0.280 | 12 | 51765746 | missense variant | G/A;T | snv | 33 | |||
rs796052243 | 0.695 | 0.520 | 4 | 122934574 | inframe deletion | CAA/- | delins | 54 | |||
rs1554121443 | 0.742 | 0.280 | 6 | 33438873 | stop gained | C/T | snv | 29 |