Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs75316749 | 0.701 | 0.280 | 3 | 169043635 | intergenic variant | A/G | snv | 4.2E-02 | 17 | ||
rs2974935 | 0.708 | 0.280 | 1 | 155212052 | non coding transcript exon variant | G/A;C;T | snv | 17 | |||
rs481519 | 0.708 | 0.280 | 3 | 27285723 | intron variant | C/A;T | snv | 17 | |||
rs11844632 | 0.708 | 0.280 | 14 | 68559662 | intron variant | G/A | snv | 0.23 | 17 | ||
rs2300206 | 0.708 | 0.280 | 20 | 34002002 | intron variant | G/C;T | snv | 17 | |||
rs7725218 | 0.708 | 0.280 | 5 | 1282299 | intron variant | G/A | snv | 0.38 | 17 | ||
rs11168936 | 0.708 | 0.280 | 12 | 49251457 | intron variant | T/A;C | snv | 17 | |||
rs10069690 | 0.595 | 0.560 | 5 | 1279675 | intron variant | C/T | snv | 0.36 | 16 | ||
rs7705526 | 0.776 | 0.240 | 5 | 1285859 | intron variant | C/A;T | snv | 15 | |||
rs10505477 | 0.658 | 0.400 | 8 | 127395198 | intron variant | A/G | snv | 0.40 | 11 | ||
rs6983267 | 0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 | 11 | ||
rs185229225 | 0.851 | 0.120 | 4 | 13607505 | intron variant | T/C | snv | 4 | |||
rs7953249 | 0.882 | 0.160 | 12 | 120965921 | splice region variant | G/A | snv | 0.59 | 4 | ||
rs11651755 | 0.763 | 0.160 | 17 | 37739849 | intron variant | T/C | snv | 0.52 | 4 | ||
rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 4 | |
rs10962692 | 0.925 | 0.120 | 9 | 16915876 | upstream gene variant | G/A;C | snv | 3 | |||
rs62274041 | 0.925 | 0.120 | 3 | 156717851 | upstream gene variant | G/A;T | snv | 3 | |||
rs1801516 | 0.627 | 0.400 | 11 | 108304735 | missense variant | G/A | snv | 0.11 | 0.11 | 3 | |
rs8170 | 0.724 | 0.160 | 19 | 17278895 | synonymous variant | G/A | snv | 0.15 | 0.18 | 3 | |
rs711830 | 0.882 | 0.120 | 2 | 176172583 | 3 prime UTR variant | A/C;G;T | snv | 0.76 | 3 | ||
rs6755777 | 0.882 | 0.120 | 2 | 176178498 | non coding transcript exon variant | T/A;G | snv | 3 | |||
rs7405776 | 0.807 | 0.120 | 17 | 37733029 | intron variant | G/A;C | snv | 3 | |||
rs2494938 | 0.752 | 0.240 | 6 | 40568389 | intron variant | G/A | snv | 0.51 | 3 | ||
rs183211 | 0.882 | 0.160 | 17 | 46710944 | intron variant | G/A | snv | 0.28 | 0.30 | 3 | |
rs2227564 | 0.763 | 0.320 | 10 | 73913343 | missense variant | T/C | snv | 0.75 | 0.81 | 3 |