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 | |||
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 | |||
rs397507549 | 0.742 | 0.240 | 12 | 112489104 | missense variant | C/A;G | snv | 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 | |||
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 | |||
rs121918455 | 0.695 | 0.440 | 12 | 112477720 | missense variant | A/C;G | snv | 1 | |||
rs121918458 | 0.807 | 0.320 | 12 | 112489080 | missense variant | T/A;G | snv | 1 | |||
rs121918462 | 0.742 | 0.320 | 12 | 112450398 | missense variant | C/T | snv | 1 | |||
rs121918463 | 0.851 | 0.240 | 12 | 112477651 | missense variant | T/A;C;G | snv | 1 | |||
rs121918464 | 0.708 | 0.440 | 12 | 112450406 | missense variant | G/A;C | snv | 1 | |||
rs121918466 | 0.752 | 0.280 | 12 | 112450416 | missense variant | A/G | snv | 1 |