Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1356791510 | 0.882 | 0.120 | 9 | 131510058 | frameshift variant | A/- | del | 8.0E-06 | 3 | ||
rs1554780670 | 0.882 | 0.120 | 9 | 131518533 | stop gained | T/G | snv | 3 | |||
rs1564364615 | 0.882 | 0.120 | 9 | 131515445 | frameshift variant | CT/- | del | 3 | |||
rs1564365317 | 0.882 | 0.120 | 9 | 131515524 | splice donor variant | T/C | snv | 3 | |||
rs200056620 | 0.882 | 0.120 | 9 | 131513243 | stop gained | C/G;T | snv | 4.0E-06; 3.6E-05 | 3 | ||
rs765230689 | 0.882 | 0.120 | 9 | 131512044 | stop gained | T/A;C | snv | 8.0E-06 | 3 | ||
rs766648827 | 0.882 | 0.120 | 9 | 131509809 | splice donor variant | G/C;T | snv | 4.0E-06 | 7.0E-06 | 3 | |
rs1453773610 | 0.882 | 0.120 | 9 | 131512039 | splice acceptor variant | A/C;T | snv | 7.0E-06 | 3 | ||
rs119462987 | 0.882 | 0.120 | 9 | 131522160 | missense variant | G/A | snv | 1.4E-05 | 3 | ||
rs149682171 | 0.882 | 0.120 | 9 | 131522113 | missense variant | C/T | snv | 6.0E-05 | 2.8E-05 | 3 | |
rs794727208 | 0.882 | 0.120 | 9 | 131521445 | stop gained | C/T | snv | 4.2E-05 | 3 | ||
rs398124245 | 0.851 | 0.120 | 9 | 131523025 | frameshift variant | -/G | delins | 2.1E-04 | 4 |