Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913527 | 0.807 | 0.320 | 12 | 25225628 | missense variant | C/A;G;T | snv | 2 | |||
rs121913240 | 0.672 | 0.440 | 12 | 25227342 | missense variant | T/A;C;G | snv | 6 | |||
rs121913361 | 0.807 | 0.280 | 7 | 140753349 | missense variant | C/A;G;T | snv | 6 | |||
rs121913502 | 0.708 | 0.320 | 15 | 90088702 | missense variant | C/A;T | snv | 3.2E-05 | 6 | ||
rs121918465 | 0.827 | 0.200 | 12 | 112450407 | missense variant | A/C;G;T | snv | 6 | |||
rs267606870 | 0.763 | 0.280 | 15 | 90088703 | missense variant | G/A;C | snv | 6 | |||
rs397507546 | 0.790 | 0.360 | 12 | 112489084 | missense variant | G/A;C;T | snv | 6 | |||
rs770248150 | 0.807 | 0.240 | 12 | 25225713 | missense variant | T/A;G | snv | 4.0E-06 | 6 | ||
rs104894231 | 0.776 | 0.360 | 11 | 533467 | missense variant | C/G;T | snv | 7 | |||
rs121917759 | 0.790 | 0.480 | 11 | 533466 | missense variant | G/A | snv | 7 | |||
rs121918464 | 0.708 | 0.440 | 12 | 112450406 | missense variant | G/A;C | snv | 7 | |||
rs121913351 | 0.776 | 0.240 | 7 | 140781611 | missense variant | C/A;G;T | snv | 4.0E-06 | 9 | ||
rs121913370 | 0.763 | 0.360 | 7 | 140753393 | missense variant | T/C;G | snv | 9 | |||
rs180177040 | 0.790 | 0.360 | 7 | 140754187 | missense variant | T/C;G | snv | 9 | |||
rs1023835002 | 0.763 | 0.280 | 15 | 44711547 | start lost | A/G;T | snv | 10 | |||
rs1057519877 | 0.763 | 0.280 | 15 | 44711549 | start lost | G/A | snv | 10 | |||
rs1057519879 | 0.763 | 0.280 | 15 | 44711548 | start lost | T/C;G | snv | 10 | |||
rs1057519933 | 0.790 | 0.240 | 3 | 179199156 | missense variant | A/G | snv | 11 | |||
rs1057519934 | 0.790 | 0.240 | 3 | 179199158 | missense variant | G/C | snv | 11 | |||
rs1057519935 | 0.790 | 0.240 | 3 | 179199157 | missense variant | A/G | snv | 11 | |||
rs121913357 | 0.742 | 0.320 | 7 | 140781603 | stop gained | C/A;G;T | snv | 11 | |||
rs397516896 | 0.763 | 0.360 | 7 | 140753355 | missense variant | C/G;T | snv | 11 | |||
rs1057519978 | 0.763 | 0.360 | 17 | 7675191 | missense variant | A/C;G;T | snv | 12 | |||
rs121913237 | 0.611 | 0.560 | 1 | 114716126 | missense variant | C/A;G;T | snv | 8.0E-06 | 12 | ||
rs121913250 | 0.683 | 0.440 | 1 | 114716127 | missense variant | C/A;G;T | snv | 12 |