Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913530 | 0.583 | 0.640 | 12 | 25245351 | missense variant | C/A;G;T | snv | 5 | |||
rs104894228 | 0.605 | 0.560 | 11 | 534286 | missense variant | C/A;G;T | snv | 2 | |||
rs104894359 | 0.851 | 0.200 | 12 | 25227346 | missense variant | C/G;T | snv | 2 | |||
rs104894366 | 0.776 | 0.400 | 12 | 25245284 | missense variant | G/A;C | snv | 2 | |||
rs121913237 | 0.611 | 0.560 | 1 | 114716126 | missense variant | C/A;G;T | snv | 8.0E-06 | 2 | ||
rs121913364 | 0.641 | 0.520 | 7 | 140753334 | missense variant | T/C;G | snv | 4.0E-06 | 2 | ||
rs121918453 | 0.732 | 0.280 | 12 | 112450394 | missense variant | G/A;C;T | snv | 2 | |||
rs121918454 | 0.742 | 0.280 | 12 | 112450395 | missense variant | C/A;G;T | snv | 2 | |||
rs121918456 | 0.752 | 0.280 | 12 | 112473023 | missense variant | A/C;G | snv | 2 | |||
rs121918461 | 0.827 | 0.240 | 12 | 112450362 | missense variant | A/C;G;T | snv | 2 | |||
rs397507510 | 0.776 | 0.280 | 12 | 112450361 | missense variant | G/A;C;T | snv | 2 | |||
rs397507511 | 0.882 | 0.240 | 12 | 112450385 | missense variant | G/A;C | snv | 2 | |||
rs397507545 | 0.708 | 0.560 | 12 | 112489083 | missense variant | G/A;C | snv | 4.0E-06 | 2 | ||
rs397507549 | 0.742 | 0.240 | 12 | 112489104 | missense variant | C/A;G | snv | 2 | |||
rs80338796 | 0.667 | 0.480 | 3 | 12604200 | missense variant | G/A;C | snv | 4.0E-06 | 2 | ||
rs80338797 | 0.827 | 0.160 | 3 | 12584624 | missense variant | G/C;T | snv | 2 | |||
rs104894229 | 0.564 | 0.600 | 11 | 534289 | missense variant | C/A;G;T | snv | 1 | |||
rs104894361 | 0.882 | 0.240 | 12 | 25245370 | missense variant | T/A;C;G | snv | 4.0E-06 | 1 | ||
rs104894364 | 0.925 | 0.160 | 12 | 25227351 | missense variant | G/A | snv | 1 | |||
rs104894365 | 0.827 | 0.320 | 12 | 25245345 | missense variant | C/T | snv | 1 | |||
rs121434594 | 0.827 | 0.160 | 3 | 12604189 | missense variant | G/A;C;T | 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 | |||
rs121913348 | 0.763 | 0.480 | 7 | 140781617 | missense variant | C/A;G;T | snv | 1 | |||
rs121913369 | 0.790 | 0.280 | 7 | 140753346 | missense variant | G/A;C | snv | 4.0E-06 | 1 |