Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs5030809 | 0.776 | 0.320 | 3 | 10142139 | missense variant | T/C | snv | 1.3E-05 | 10 | ||
rs28940298 | 0.776 | 0.280 | 3 | 10149921 | missense variant | C/T | snv | 2.1E-04 | 1.0E-04 | 9 | |
rs5030824 | 0.776 | 0.320 | 3 | 10149885 | missense variant | C/G | snv | 2.0E-05 | 4.2E-05 | 9 | |
rs5030821 | 0.827 | 0.280 | 3 | 10149823 | missense variant | G/A;C;T | snv | 4.0E-06 | 8 | ||
rs730882035 | 0.807 | 0.200 | 3 | 10149805 | missense variant | G/A | snv | 7 | |||
rs5030820 | 0.827 | 0.280 | 3 | 10149822 | missense variant | C/G;T | snv | 8.0E-06 | 6 | ||
rs5030807 | 0.851 | 0.320 | 3 | 10142113 | missense variant | T/A;C | snv | 5 | |||
rs104893826 | 0.882 | 0.200 | 3 | 10142038 | missense variant | G/A;C | snv | 4 | |||
rs104893831 | 0.925 | 0.040 | 3 | 10146549 | missense variant | G/A;C;T | snv | 2.0E-05 | 4 | ||
rs397516441 | 0.882 | 0.200 | 3 | 10149790 | missense variant | A/G | snv | 4 | |||
rs5030818 | 0.882 | 0.280 | 3 | 10149804 | stop gained | C/G;T | snv | 4 | |||
rs5030827 | 0.882 | 0.200 | 3 | 10142097 | missense variant | G/A;C;T | snv | 4.4E-06 | 4 | ||
rs869025621 | 0.882 | 0.240 | 3 | 10142079 | missense variant | A/C;G;T | snv | 4 | |||
rs104893830 | 0.925 | 0.160 | 3 | 10146561 | missense variant | G/C;T | snv | 3 | |||
rs119103277 | 0.925 | 0.160 | 3 | 10142110 | stop gained | G/A;C | snv | 3 | |||
rs121913346 | 0.925 | 0.240 | 3 | 10149796 | missense variant | T/A;C | snv | 3 | |||
rs1553619976 | 0.925 | 0.160 | 3 | 10146593 | frameshift variant | -/A | delins | 3 | |||
rs193922613 | 0.925 | 0.160 | 3 | 10149847 | missense variant | A/G;T | snv | 3 | |||
rs5030622 | 0.925 | 0.160 | 3 | 10149809 | stop gained | C/A;G | snv | 3 | |||
rs5030804 | 0.925 | 0.160 | 3 | 10142080 | missense variant | A/C;G;T | snv | 3 | |||
rs5030816 | 0.925 | 0.160 | 3 | 10149785 | splice acceptor variant | A/G;T | snv | 3 | |||
rs5030822 | 0.925 | 0.160 | 3 | 10149856 | missense variant | T/A;C;G | snv | 3 | |||
rs5030830 | 0.925 | 0.160 | 3 | 10146526 | missense variant | T/C;G | snv | 3 | |||
rs5030833 | 0.925 | 0.160 | 3 | 10146580 | missense variant | T/C;G | snv | 4.0E-06 | 3 | ||
rs730882034 | 0.925 | 0.160 | 3 | 10142104 | missense variant | C/G;T | snv | 3 |