Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1555454508 | 0.790 | 0.240 | 15 | 44615487 | stop gained | GTA/ATC | mnv | 18 | |||
rs312262717 | 0.790 | 0.240 | 15 | 44659104 | frameshift variant | A/-;AA | delins | 18 | |||
rs174576 | 0.851 | 0.200 | 11 | 61836038 | intron variant | C/A;T | snv | 12 | |||
rs12443954 | 0.851 | 0.040 | 16 | 89675088 | intron variant | A/C;G | snv | 5 | |||
rs17693963 | 0.882 | 0.040 | 6 | 27742386 | upstream gene variant | A/C;G | snv | 5 | |||
rs2535629 | 0.827 | 0.040 | 3 | 52799203 | intron variant | G/A;C | snv | 5 | |||
rs2721800 | 0.851 | 0.040 | 7 | 24652933 | intron variant | G/A;C;T | snv | 5 | |||
rs28456 | 0.925 | 0.120 | 11 | 61822009 | intron variant | A/C;G | snv | 5 | |||
rs9297357 | 0.851 | 0.040 | 8 | 105130105 | intron variant | C/G;T | snv | 5 | |||
rs9951150 | 0.851 | 0.040 | 18 | 55153893 | intergenic variant | A/G;T | snv | 5 | |||
rs11829119 | 0.851 | 0.040 | 12 | 19040597 | intergenic variant | T/A;C | snv | 4 | |||
rs141252918 | 0.882 | 0.040 | 6 | 151506923 | intron variant | G/A;C | snv | 4 | |||
rs17154917 | 0.851 | 0.040 | 7 | 81207393 | intergenic variant | G/A;T | snv | 4 | |||
rs17211233 | 0.882 | 0.040 | 5 | 81072944 | intron variant | T/A;C | snv | 4 | |||
rs2054399 | 0.925 | 0.040 | 3 | 178623794 | intron variant | G/A;C | snv | 4 | |||
rs221774 | 0.851 | 0.080 | 7 | 100701361 | upstream gene variant | A/G;T | snv | 4 | |||
rs5742905 | 0.701 | 0.360 | 21 | 43063074 | missense variant | A/G | snv | 4 | |||
rs9862857 | 0.851 | 0.040 | 3 | 30453840 | regulatory region variant | A/G;T | snv | 4 | |||
rs105633 | 0.882 | 0.040 | 5 | 141945684 | synonymous variant | T/C;G | snv | 0.98; 4.0E-06 | 3 | ||
rs10744560 | 0.882 | 0.040 | 12 | 2277933 | intron variant | C/G;T | snv | 3 | |||
rs11125080 | 0.882 | 0.040 | 2 | 46505266 | intron variant | G/A;C | snv | 3 | |||
rs12052005 | 0.882 | 0.040 | 18 | 68832311 | intron variant | G/C;T | snv | 3 | |||
rs12149074 | 1.000 | 0.040 | 16 | 80071969 | intron variant | C/A;G | snv | 3 | |||
rs138449918 | 0.882 | 0.040 | 2 | 39936810 | intron variant | AT/-;ATAT | delins | 3 | |||
rs1906252 | 0.925 | 0.120 | 6 | 98102413 | intron variant | C/A;T | snv | 3 |