Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6983267 | 0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 | 62 | ||
rs28934578 | 0.605 | 0.600 | 17 | 7675088 | missense variant | C/A;T | snv | 4.0E-06 | 47 | ||
rs6259 | 0.658 | 0.400 | 17 | 7633209 | missense variant | G/A | snv | 8.9E-02 | 8.1E-02 | 27 | |
rs523349 | 0.689 | 0.440 | 2 | 31580636 | missense variant | G/A;C;T | snv | 0.66; 4.9E-06 | 21 | ||
rs10993994 | 0.763 | 0.280 | 10 | 46046326 | 5 prime UTR variant | A/G | snv | 0.54 | 15 | ||
rs627928 | 0.790 | 0.080 | 1 | 182582202 | missense variant | A/C | snv | 0.54 | 0.49 | 10 | |
rs4242382 | 0.763 | 0.240 | 8 | 127505328 | intergenic variant | A/G;T | snv | 9 | |||
rs2011077 | 0.807 | 0.080 | 5 | 177094455 | intron variant | C/T | snv | 0.19 | 8 | ||
rs976306779 | 0.851 | 0.080 | X | 67545492 | missense variant | C/A;T | snv | 6.6E-06 | 8 | ||
rs41341748 | 0.827 | 0.120 | 8 | 16155085 | stop gained | G/A;C | snv | 8.3E-03; 2.8E-05 | 6 | ||
rs1374051619 | 0.827 | 0.080 | 17 | 12995026 | missense variant | C/G | snv | 4.0E-06 | 5 | ||
rs1870050 | 0.827 | 0.160 | 15 | 51344354 | intron variant | A/C | snv | 6.0E-02 | 5 | ||
rs544190 | 0.851 | 0.080 | 9 | 76763591 | intron variant | G/A | snv | 0.32 | 4 | ||
rs765521022 | 0.851 | 0.080 | 19 | 50858171 | missense variant | T/C | snv | 4 | |||
rs2208532 | 0.882 | 0.080 | 2 | 31563919 | intron variant | G/A | snv | 0.59 | 3 | ||
rs56350726 | 0.882 | 0.080 | 9 | 84285454 | missense variant | T/A;C | snv | 7.2E-02; 1.2E-05 | 3 | ||
rs676033 | 0.882 | 0.080 | 2 | 31583901 | upstream gene variant | T/C | snv | 0.69 | 3 | ||
rs12030724 | 0.925 | 0.080 | 1 | 42694347 | intron variant | A/T | snv | 8.9E-02 | 2 |