Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1085308041 | 0.763 | 0.160 | 10 | 87965285 | splice acceptor variant | A/C;G | snv | 12 | |||
rs121909232 | 0.776 | 0.160 | 10 | 87952258 | stop gained | C/A;G | snv | 4.0E-06 | 9 | ||
rs786201041 | 0.776 | 0.160 | 10 | 87961119 | splice donor variant | G/A;C | snv | 9 | |||
rs1060500126 | 0.790 | 0.160 | 10 | 87933223 | missense variant | A/C;G | snv | 8 | |||
rs1114167621 | 0.790 | 0.160 | 10 | 87931045 | splice acceptor variant | G/A;C;T | snv | 8 | |||
rs1114167622 | 0.790 | 0.160 | 10 | 87952260 | splice donor variant | G/C | snv | 8 | |||
rs1114167640 | 0.790 | 0.160 | 10 | 87961067 | stop gained | TGACAAAGCAAATA/CGCTT | delins | 8 | |||
rs1114167650 | 0.790 | 0.160 | 10 | 87925562 | splice region variant | G/A | snv | 8 | |||
rs121909223 | 0.790 | 0.160 | 10 | 87933129 | missense variant | T/C;G | snv | 8 | |||
rs121909225 | 0.790 | 0.160 | 10 | 87894049 | missense variant | T/C;G | snv | 8 | |||
rs121909241 | 0.790 | 0.160 | 10 | 87933154 | missense variant | G/A;T | snv | 8 | |||
rs138336847 | 0.790 | 0.160 | 10 | 87952264 | splice region variant | G/A;C | snv | 4.0E-06 | 8 | ||
rs398123317 | 0.790 | 0.160 | 10 | 87925550 | missense variant | T/A;C;G | snv | 8 | |||
rs587781784 | 0.790 | 0.160 | 10 | 87952116 | splice acceptor variant | A/C;G;T | snv | 8 | |||
rs587782350 | 0.776 | 0.160 | 10 | 87957955 | missense variant | C/T | snv | 8 | |||
rs587782455 | 0.790 | 0.160 | 10 | 87960892 | splice acceptor variant | A/G;T | snv | 5.1E-05 | 8 | ||
rs727504114 | 0.790 | 0.160 | 10 | 87952261 | splice donor variant | T/C;G | snv | 8 | |||
rs786203847 | 0.790 | 0.160 | 10 | 87925512 | splice acceptor variant | G/A;C | snv | 8 | |||
rs121909221 | 0.790 | 0.160 | 10 | 87952135 | missense variant | T/A | snv | 7 | |||
rs121909226 | 0.790 | 0.160 | 10 | 87925557 | missense variant | T/C | snv | 7 | |||
rs121909228 | 0.790 | 0.160 | 10 | 87957984 | stop gained | G/T | snv | 7 | |||
rs1554825165 | 0.790 | 0.160 | 10 | 87957872 | stop gained | C/A | snv | 7 | |||
rs1554825530 | 0.790 | 0.160 | 10 | 87960957 | frameshift variant | -/CT;TTCT | ins | 7 | |||
rs1554825643 | 0.790 | 0.160 | 10 | 87961107 | frameshift variant | C/- | delins | 7 | |||
rs1554897854 | 0.790 | 0.160 | 10 | 87931042 | splice acceptor variant | AGTT/- | delins | 7 |