Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104894201 | 0.763 | 0.280 | 11 | 111908934 | missense variant | T/C | snv | 12 | |||
rs1114167307 | 0.851 | 0.200 | 13 | 20143233 | missense variant | G/A | snv | 4 | |||
rs150857132 | 0.851 | 0.200 | 2 | 208124183 | missense variant | C/A;T | snv | 4.4E-04; 4.0E-06 | 4 | ||
rs28931605 | 0.807 | 0.200 | 2 | 208124294 | missense variant | G/A;T | snv | 4.2E-06; 1.3E-05 | 6 | ||
rs398122944 | 0.851 | 0.200 | 2 | 208128257 | stop gained | C/G;T | snv | 4 | |||
rs587778872 | 0.807 | 0.200 | 2 | 208128231 | missense variant | G/A;C | snv | 8.0E-06 | 6 | ||
rs1463326176 | 0.851 | 0.200 | 2 | 208124291 | frameshift variant | TGGG/- | del | 4 |