Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs61816761 | 0.658 | 0.640 | 1 | 152313385 | stop gained | G/A;T | snv | 9.4E-03; 8.0E-06 | 28 | ||
rs2155219 | 0.732 | 0.280 | 11 | 76588150 | upstream gene variant | G/T | snv | 0.52 | 12 | ||
rs10445308 | 0.851 | 0.240 | 17 | 39781794 | intron variant | C/T | snv | 0.38 | 5 | ||
rs1295685 | 0.790 | 0.160 | 5 | 132660753 | 3 prime UTR variant | A/G | snv | 0.81 | 5 | ||
rs479844 | 0.851 | 0.160 | 11 | 65784486 | upstream gene variant | A/G | snv | 0.44 | 5 | ||
rs6871536 | 0.827 | 0.160 | 5 | 132634182 | intron variant | T/C | snv | 0.24 | 3 | ||
rs12081541 | 0.925 | 0.160 | 1 | 152468890 | intergenic variant | T/C | snv | 8.9E-02 | 2 | ||
rs17690965 | 0.925 | 0.160 | 5 | 132694975 | 3 prime UTR variant | C/G | snv | 0.57 | 2 | ||
rs9357733 | 0.851 | 0.160 | 6 | 52427338 | intron variant | A/G | snv | 0.19 | 2 | ||
rs993226 | 0.851 | 0.160 | 12 | 84492794 | intergenic variant | T/G | snv | 6.3E-02 | 2 |