Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913279 | 0.526 | 0.560 | 3 | 179234297 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 48 | ||
rs121909224 | 0.627 | 0.560 | 10 | 87933147 | stop gained | C/G;T | snv | 1.2E-05 | 35 | ||
rs121909231 | 0.667 | 0.600 | 10 | 87961095 | stop gained | C/A;T | snv | 29 | |||
rs121909219 | 0.689 | 0.400 | 10 | 87957915 | stop gained | C/A;T | snv | 24 | |||
rs121909229 | 0.683 | 0.400 | 10 | 87933148 | missense variant | G/A;C;T | snv | 23 | |||
rs121913293 | 0.732 | 0.360 | 10 | 87952142 | missense variant | C/A;T | snv | 18 | |||
rs121909218 | 0.672 | 0.360 | 10 | 87933145 | missense variant | G/A | snv | 14 | |||
rs587776667 | 0.742 | 0.280 | 10 | 87931090 | splice donor variant | G/A;C;T | snv | 14 | |||
rs863224909 | 0.732 | 0.360 | 10 | 87960952 | stop gained | C/A;G | snv | 14 | |||
rs370795352 | 0.742 | 0.360 | 10 | 87933163 | missense variant | T/A;C | snv | 4.0E-06 | 13 | ||
rs1085308041 | 0.763 | 0.160 | 10 | 87965285 | splice acceptor variant | A/C;G | snv | 12 | |||
rs1085308043 | 0.763 | 0.200 | 10 | 87925511 | splice acceptor variant | A/G;T | snv | 12 | |||
rs1224040268 | 0.742 | 0.360 | 10 | 87931091 | splice donor variant | T/A;C | snv | 7.0E-06 | 12 | ||
rs876661024 | 0.776 | 0.200 | 10 | 87957852 | splice acceptor variant | G/A;C;T | snv | 11 | |||
rs1064793345 | 0.752 | 0.240 | 10 | 87961039 | missense variant | T/C | snv | 10 | |||
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 | |||
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 | |||
rs121909227 | 0.776 | 0.240 | 10 | 87957858 | stop gained | C/T | snv | 8 | |||
rs121909241 | 0.790 | 0.160 | 10 | 87933154 | missense variant | G/A;T | snv | 8 |