Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs63750424 | 0.677 | 0.240 | 17 | 46024061 | missense variant | C/T | snv | 1.6E-05 | 30 | ||
rs63750215 | 0.701 | 0.240 | 1 | 226885603 | missense variant | A/T | snv | 19 | |||
rs781049584 | 0.724 | 0.280 | 21 | 26021917 | missense variant | T/G | snv | 8.2E-06 | 7.0E-06 | 18 | |
rs63750264 | 0.716 | 0.360 | 21 | 25891784 | missense variant | C/A;G;T | snv | 17 | |||
rs3091244 | 0.724 | 0.280 | 1 | 159714875 | upstream gene variant | G/A;T | snv | 17 | |||
rs2794521 | 0.742 | 0.480 | 1 | 159715306 | upstream gene variant | C/T | snv | 0.78 | 15 | ||
rs63750579 | 0.742 | 0.280 | 21 | 25891856 | missense variant | C/G;T | snv | 13 | |||
rs74315409 | 0.742 | 0.240 | 20 | 4699915 | missense variant | T/G | snv | 6.0E-05 | 2.1E-05 | 13 | |
rs1035071612 | 0.763 | 0.240 | 19 | 11113361 | missense variant | C/A;T | snv | 4.0E-06 | 9 | ||
rs63750671 | 0.790 | 0.240 | 21 | 25891858 | missense variant | G/C | snv | 8 | |||
rs63750311 | 0.790 | 0.240 | 14 | 73192647 | missense variant | A/C | snv | 8 | |||
rs63750522 | 0.827 | 0.120 | 14 | 73173644 | missense variant | G/A;C | snv | 8 | |||
rs765670175 | 0.790 | 0.120 | 14 | 73173646 | missense variant | T/A | snv | 8.0E-06 | 7 | ||
rs3093075 | 0.882 | 0.120 | 1 | 159710123 | upstream gene variant | G/T | snv | 0.13 | 5 | ||
rs79524815 | 0.851 | 0.240 | 7 | 18658708 | intron variant | T/G | snv | 3.8E-02 | 4 | ||
rs34487851 | 0.882 | 0.200 | 2 | 106026098 | regulatory region variant | A/G | snv | 0.28 | 3 | ||
rs1412095491 | 0.882 | 0.200 | 21 | 26051053 | missense variant | C/G | snv | 4.0E-06 | 3 | ||
rs6910730 | 0.925 | 0.080 | 6 | 41278895 | intron variant | A/G | snv | 0.21 | 3 | ||
rs191838178 | 0.925 | 0.160 | 22 | 40407449 | missense variant | C/T | snv | 2.4E-05 | 7.0E-06 | 2 | |
rs10908821 | 1.000 | 0.040 | 1 | 161038745 | intron variant | C/G | snv | 0.11 | 1 | ||
rs2774276 | 1.000 | 0.040 | 1 | 161041926 | intron variant | G/A;C | snv | 1 |