Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs61753219 | 0.672 | 0.400 | 6 | 42978330 | missense variant | G/A | snv | 3.6E-05 | 2.8E-05 | 64 | |
rs1010184002 | 0.689 | 0.400 | 6 | 42978878 | stop gained | C/T | snv | 7.0E-06 | 60 | ||
rs104894228 | 0.605 | 0.560 | 11 | 534286 | missense variant | C/A;G;T | snv | 48 | |||
rs121918459 | 0.662 | 0.440 | 12 | 112450368 | missense variant | A/G | snv | 1.2E-05 | 7.0E-06 | 47 | |
rs28933068 | 0.645 | 0.560 | 4 | 1805644 | missense variant | C/A;G;T | snv | 1.6E-05 | 30 | ||
rs3782886 | 0.724 | 0.480 | 12 | 111672685 | synonymous variant | T/C | snv | 1.9E-02 | 5.9E-03 | 22 | |
rs28931614 | 0.672 | 0.520 | 4 | 1804392 | missense variant | G/A;C | snv | 21 | |||
rs121913485 | 0.716 | 0.400 | 4 | 1804372 | missense variant | A/G | snv | 18 | |||
rs267607048 | 0.752 | 0.560 | 10 | 110964362 | missense variant | A/G | snv | 7.0E-06 | 16 | ||
rs121918456 | 0.752 | 0.280 | 12 | 112473023 | missense variant | A/C;G | snv | 13 | |||
rs587781858 | 0.742 | 0.360 | 17 | 7669671 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06 | 12 | ||
rs397515453 | 0.752 | 0.440 | 5 | 68296301 | missense variant | C/T | snv | 11 | |||
rs121913479 | 0.763 | 0.280 | 4 | 1804362 | missense variant | G/A;T | snv | 4.0E-06 | 10 | ||
rs1566902569 | 0.882 | 0.160 | 15 | 48460299 | missense variant | C/A | snv | 9 | |||
rs587779349 | 0.776 | 0.280 | 13 | 32380040 | frameshift variant | C/- | delins | 8 | |||
rs1131691804 | 0.807 | 0.200 | 15 | 48463123 | missense variant | G/A | snv | 8 | |||
rs104894419 | 0.807 | 0.360 | 13 | 108208829 | stop gained | G/A | snv | 9.9E-05 | 7.0E-05 | 8 | |
rs60864230 | 0.790 | 0.280 | 1 | 156130658 | missense variant | G/A;C;T | snv | 4.0E-06 | 7 | ||
rs1555545033 | 0.807 | 0.160 | 17 | 40088306 | missense variant | C/T | snv | 7 | |||
rs2076738 | 0.807 | 0.200 | 8 | 132906843 | missense variant | T/C | snv | 1.6E-05 | 7.0E-06 | 6 | |
rs587779351 | 0.851 | 0.200 | 5 | 83105046 | missense variant | T/C | snv | 1.6E-05 | 6 | ||
rs121918010 | 0.827 | 0.200 | 1 | 21573781 | missense variant | T/C | snv | 7.2E-05 | 4.2E-05 | 5 | |
rs122460151 | 0.851 | 0.280 | X | 2958423 | missense variant | C/G | snv | 7.1E-05 | 3.8E-05 | 5 | |
rs1481733213 | 0.851 | 0.240 | 3 | 142568059 | splice region variant | T/C | snv | 5 | |||
rs1553761113 | 0.851 | 0.240 | 3 | 142507967 | missense variant | C/A | snv | 5 |