Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2867125 | 0.925 | 0.120 | 2 | 622827 | intergenic variant | T/A;C | snv | 0.85 | 6 | ||
rs2943634 | 0.763 | 0.200 | 2 | 226203364 | intergenic variant | A/C;G | snv | 8 | |||
rs329122 | 1.000 | 0.080 | 5 | 134528909 | intron variant | G/A | snv | 0.45 | 2 | ||
rs340874 | 0.882 | 0.080 | 1 | 213985913 | non coding transcript exon variant | T/C | snv | 0.40 | 4 | ||
rs35261542 | 1.000 | 0.080 | 6 | 20675561 | intron variant | C/A | snv | 0.26 | 3 | ||
rs3751812 | 0.882 | 0.160 | 16 | 53784548 | intron variant | G/T | snv | 0.30 | 7 | ||
rs3802177 | 1.000 | 0.080 | 8 | 117172786 | 3 prime UTR variant | G/A | snv | 0.24 | 4 | ||
rs4420638 | 0.708 | 0.520 | 19 | 44919689 | downstream gene variant | A/G | snv | 0.18 | 36 | ||
rs4506565 | 0.790 | 0.280 | 10 | 112996282 | intron variant | A/G;T | snv | 19 | |||
rs4865796 | 1.000 | 0.080 | 5 | 53976834 | intron variant | G/A | snv | 0.72 | 3 | ||
rs562338 | 0.807 | 0.160 | 2 | 21065449 | intergenic variant | A/G | snv | 0.69 | 20 | ||
rs6857 | 0.790 | 0.240 | 19 | 44888997 | 3 prime UTR variant | C/T | snv | 0.13 | 15 | ||
rs6947395 | 1.000 | 0.080 | 7 | 69941675 | intron variant | A/T | snv | 0.20 | 2 | ||
rs7020996 | 0.925 | 0.120 | 9 | 22129580 | downstream gene variant | C/A;T | snv | 3 | |||
rs7034200 | 1.000 | 0.080 | 9 | 4289050 | intron variant | C/A;G | snv | 3 | |||
rs7144011 | 1.000 | 0.080 | 14 | 79474040 | intron variant | G/T | snv | 0.21 | 4 | ||
rs7173964 | 1.000 | 0.080 | 15 | 62104743 | regulatory region variant | G/A | snv | 0.49 | 3 | ||
rs7185735 | 0.925 | 0.120 | 16 | 53788739 | intron variant | A/G;T | snv | 5 | |||
rs7193144 | 0.925 | 0.120 | 16 | 53776774 | intron variant | T/C | snv | 0.40 | 5 | ||
rs7202116 | 0.882 | 0.120 | 16 | 53787703 | intron variant | A/G | snv | 0.41 | 6 | ||
rs72892910 | 1.000 | 0.080 | 6 | 50849174 | downstream gene variant | G/T | snv | 0.17 | 2 | ||
rs7374732 | 1.000 | 0.080 | 3 | 23161963 | regulatory region variant | C/T | snv | 0.73 | 4 | ||
rs7570971 | 1.000 | 0.080 | 2 | 135080336 | intron variant | C/A | snv | 0.61 | 5 | ||
rs7578326 | 0.882 | 0.080 | 2 | 226155937 | TF binding site variant | A/G | snv | 0.36 | 3 | ||
rs76895963 | 1.000 | 0.080 | 12 | 4275678 | intron variant | T/G | snv | 1.5E-02 | 6 |