Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11117432 | 0.851 | 0.200 | 16 | 85985665 | upstream gene variant | G/A | snv | 0.15 | 1 | ||
rs12134279 | 0.925 | 0.080 | 1 | 197812068 | regulatory region variant | C/T | snv | 0.17 | 1 | ||
rs4679904 | 0.925 | 0.080 | 3 | 160623108 | intergenic variant | C/G;T | snv | 1 | |||
rs860413 | 0.925 | 0.080 | 5 | 35942940 | upstream gene variant | A/C | snv | 0.23 | 1 | ||
rs968451 | 0.925 | 0.080 | 22 | 39274846 | intron variant | G/T | snv | 0.18 | 1 | ||
rs4938534 | 0.925 | 0.080 | 11 | 111404408 | intron variant | G/A | snv | 0.56 | 1 | ||
rs7665590 | 0.925 | 0.080 | 4 | 98875633 | 3 prime UTR variant | T/C | snv | 0.56 | 1 | ||
rs8017161 | 0.925 | 0.080 | 14 | 103096858 | intron variant | G/A | snv | 0.38 | 1 | ||
rs6441286 | 0.925 | 0.080 | 3 | 160011091 | intron variant | T/G | snv | 0.36 | 1 | ||
rs3790567 | 0.851 | 0.240 | 1 | 67356694 | intron variant | A/G | snv | 0.61 | 1 | ||
rs485499 | 0.925 | 0.080 | 3 | 160028076 | intron variant | T/C | snv | 0.29 | 1 | ||
rs6890853 | 0.925 | 0.080 | 5 | 35852209 | upstream gene variant | G/A | snv | 0.25 | 1 | ||
rs7665090 | 0.807 | 0.280 | 4 | 102630446 | downstream gene variant | A/G | snv | 0.55 | 1 | ||
rs10931468 | 0.925 | 0.080 | 2 | 190673836 | intron variant | C/A;G;T | snv | 1 | |||
rs1372072 | 0.851 | 0.200 | 3 | 16913767 | intron variant | G/A | snv | 0.35 | 1 | ||
rs911263 | 0.851 | 0.200 | 14 | 68286876 | intron variant | C/T | snv | 0.57 | 1 | ||
rs538147 | 0.925 | 0.080 | 11 | 64362250 | intron variant | G/A | snv | 0.29 | 1 | ||
rs3745516 | 0.925 | 0.080 | 19 | 50423485 | intron variant | A/G | snv | 0.62 | 1 | ||
rs12924729 | 0.882 | 0.200 | 16 | 11093926 | intron variant | G/A | snv | 0.34 | 2 | ||
rs6974491 | 0.807 | 0.120 | 7 | 37334906 | intron variant | G/A | snv | 0.14 | 2 | ||
rs7208487 | 0.925 | 0.080 | 17 | 39387196 | intron variant | T/A;G | snv | 2 | |||
rs2293370 | 0.882 | 0.160 | 3 | 119501087 | intron variant | G/A | snv | 0.18 | 2 | ||
rs1800693 | 0.776 | 0.360 | 12 | 6330843 | non coding transcript exon variant | T/C | snv | 0.36; 4.0E-06 | 0.38 | 2 | |
rs4979462 | 0.790 | 0.240 | 9 | 114804733 | intron variant | C/T | snv | 0.13 | 2 | ||
rs12531711 | 0.827 | 0.200 | 7 | 128977412 | intron variant | A/C;G | snv | 2 |