Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121909646 | 0.882 | 0.120 | 13 | 28018504 | missense variant | T/A;G | snv | 1 | |||
rs121912472 | 0.925 | 0.080 | 9 | 5073742 | missense variant | G/C | snv | 1 | |||
rs121913232 | 0.925 | 0.120 | 13 | 28018500 | missense variant | G/C | snv | 1 | |||
rs121913233 | 0.627 | 0.520 | 11 | 533874 | missense variant | T/A;C;G | snv | 1 | |||
rs121913240 | 0.672 | 0.440 | 12 | 25227342 | missense variant | T/A;C;G | snv | 1 | |||
rs121913250 | 0.683 | 0.440 | 1 | 114716127 | missense variant | C/A;G;T | snv | 1 | |||
rs121913488 | 0.807 | 0.120 | 13 | 28018505 | missense variant | C/A;G;T | snv | 1 | |||
rs121913503 | 0.689 | 0.200 | 15 | 90088606 | missense variant | C/A;T | snv | 1 | |||
rs121913514 | 0.763 | 0.240 | 4 | 54733174 | missense variant | T/A;G | snv | 1 | |||
rs121917759 | 0.790 | 0.480 | 11 | 533466 | missense variant | G/A | snv | 1 | |||
rs121918464 | 0.708 | 0.440 | 12 | 112450406 | missense variant | G/A;C | snv | 1 | |||
rs137854451 | 0.925 | 0.080 | 19 | 856000 | missense variant | G/A | snv | 1 | |||
rs267606870 | 0.763 | 0.280 | 15 | 90088703 | missense variant | G/A;C | snv | 1 | |||
rs28931590 | 1.000 | 0.040 | 19 | 33302164 | missense variant | T/A | snv | 1 | |||
rs28933406 | 0.667 | 0.480 | 11 | 533875 | missense variant | G/C;T | snv | 1 | |||
rs387906629 | 0.925 | 0.080 | 3 | 128481270 | missense variant | G/A | snv | 1 | |||
rs483352695 | 0.882 | 0.200 | 17 | 7674227 | missense variant | T/A;C;G | snv | 1 | |||
rs57246956 | 0.882 | 0.080 | 19 | 855649 | missense variant | G/A;T | snv | 1 | |||
rs587781288 | 0.732 | 0.440 | 17 | 7675190 | missense variant | C/A;T | snv | 1 | |||
rs587782529 | 0.851 | 0.200 | 17 | 7670700 | missense variant | G/A;C | snv | 1 | |||
rs74315450 | 0.851 | 0.120 | 21 | 34859485 | missense variant | C/T | snv | 1 | |||
rs786201838 | 0.683 | 0.440 | 17 | 7674953 | missense variant | T/A;C;G | snv | 1 | |||
rs869312828 | 0.807 | 0.080 | 5 | 177512369 | missense variant | C/T | snv | 1 |