Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs210143 | 0.827 | 0.160 | 6 | 33579153 | intron variant | T/C | snv | 0.74 | 1 | ||
rs2285803 | 0.925 | 0.160 | 6 | 31139481 | intron variant | T/C | snv | 0.72 | 2 | ||
rs1672753 | 0.882 | 0.240 | 3 | 3179746 | upstream gene variant | C/T | snv | 0.71 | 4 | ||
rs25487 | 0.441 | 0.800 | 19 | 43551574 | missense variant | T/C | snv | 0.68 | 0.71 | 205 | |
rs1800795 | 0.494 | 0.840 | 7 | 22727026 | intron variant | C/G | snv | 0.71 | 140 | ||
rs2010963 | 0.542 | 0.840 | 6 | 43770613 | 5 prime UTR variant | C/G | snv | 0.68 | 81 | ||
rs6457327 | 0.790 | 0.320 | 6 | 31106253 | downstream gene variant | A/C | snv | 0.66 | 4 | ||
rs1128503 | 0.564 | 0.760 | 7 | 87550285 | synonymous variant | A/G | snv | 0.54 | 0.63 | 64 | |
rs4351714 | 1.000 | 0.160 | 1 | 202791530 | intron variant | T/C | snv | 0.61 | 1 | ||
rs1884444 | 0.637 | 0.600 | 1 | 67168129 | missense variant | G/T | snv | 0.52 | 0.51 | 34 | |
rs4284505 | 1.000 | 0.160 | 13 | 91349218 | non coding transcript exon variant | A/G | snv | 0.51 | 1 | ||
rs711613 | 1.000 | 0.160 | 3 | 3178805 | intron variant | T/C | snv | 0.51 | 1 | ||
rs1056836 | 0.581 | 0.680 | 2 | 38071060 | missense variant | G/C | snv | 0.51 | 58 | ||
rs1419881 | 0.851 | 0.280 | 6 | 31162816 | 3 prime UTR variant | G/A | snv | 0.50 | 2 | ||
rs710190 | 0.925 | 0.200 | 22 | 39131785 | 3 prime UTR variant | T/C | snv | 0.48 | 1 | ||
rs7336610 | 0.827 | 0.240 | 13 | 91352883 | intron variant | C/T | snv | 0.47 | 5 | ||
rs2151280 | 0.701 | 0.360 | 9 | 22034720 | non coding transcript exon variant | G/A | snv | 0.46 | 11 | ||
rs1801394 | 0.531 | 0.840 | 5 | 7870860 | missense variant | A/G | snv | 0.47 | 0.45 | 101 | |
rs13409 | 1.000 | 0.160 | 6 | 31164363 | 3 prime UTR variant | G/A | snv | 0.44 | 1 | ||
rs1049623 | 0.925 | 0.200 | 6 | 30897052 | synonymous variant | T/C | snv | 0.47 | 0.43 | 2 | |
rs877529 | 1.000 | 0.160 | 22 | 39146287 | intron variant | G/A | snv | 0.43 | 1 | ||
rs9344 | 0.653 | 0.480 | 11 | 69648142 | splice region variant | G/A | snv | 0.45 | 0.39 | 30 | |
rs12717 | 0.925 | 0.160 | 6 | 170553212 | missense variant | G/C | snv | 0.42 | 0.38 | 2 | |
rs6465657 | 0.807 | 0.280 | 7 | 98187015 | intron variant | C/T | snv | 0.41 | 0.37 | 4 | |
rs3087243 | 0.623 | 0.720 | 2 | 203874196 | downstream gene variant | G/A | snv | 0.37 | 35 |