Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs119455955 | 0.851 | 0.120 | 11 | 6617040 | stop gained | G/A | snv | 2.2E-04 | 2.4E-04 | 4 | |
rs202189057 | 0.925 | 0.120 | 11 | 6617695 | stop gained | A/T | snv | 4.0E-06 | 2 | ||
rs756564767 | 0.882 | 0.120 | 11 | 6617627 | stop gained | G/A | snv | 6.4E-05 | 4.2E-05 | 3 | |
rs786204753 | 0.925 | 0.120 | 11 | 6615217 | stop gained | C/T | snv | 2 | |||
rs119455954 | 0.925 | 0.120 | 11 | 6616056 | missense variant | C/T | snv | 1.6E-05 | 4.9E-05 | 2 | |
rs119455957 | 0.882 | 0.120 | 11 | 6616696 | missense variant | C/A | snv | 8.0E-06 | 7.0E-06 | 3 | |
rs121908199 | 0.925 | 0.120 | 11 | 6615542 | missense variant | C/T | snv | 2 | |||
rs121908200 | 0.925 | 0.120 | 11 | 6615442 | missense variant | C/G | snv | 2.0E-05 | 2.1E-05 | 2 | |
rs121908202 | 0.925 | 0.120 | 11 | 6615172 | missense variant | G/A | snv | 2.4E-05 | 2 | ||
rs121908209 | 0.925 | 0.120 | 11 | 6617045 | missense variant | C/G;T | snv | 4.0E-06; 4.0E-06 | 2 | ||
rs763162812 | 0.925 | 0.120 | 11 | 6616720 | missense variant | T/A | snv | 1.6E-05 | 2.8E-05 | 2 | |
rs765380155 | 0.925 | 0.120 | 11 | 6616374 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 2 | |
rs113019349 | 0.925 | 0.120 | 11 | 6616004 | splice donor variant | C/G;T | snv | 2 | |||
rs1554902216 | 0.925 | 0.120 | 11 | 6618820 | frameshift variant | AG/- | delins | 2 | |||
rs1554902052 | 0.925 | 0.120 | 11 | 6617430 | splice acceptor variant | T/C | snv | 2 | |||
rs56144125 | 0.827 | 0.240 | 11 | 6617154 | splice acceptor variant | C/A;G;T | snv | 4.0E-04; 1.2E-05 | 6 | ||
rs1564855725 | 0.882 | 0.160 | 11 | 6617621 | splice region variant | C/T | snv | 5 |