Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1258159645 | 0.630 | 0.600 | 16 | 69711128 | missense variant | G/A | snv | 7.0E-06 | 37 | ||
rs2187668 | 0.701 | 0.480 | 6 | 32638107 | intron variant | C/T | snv | 3.3E-03 | 20 | ||
rs5743708 | 0.525 | 0.800 | 4 | 153705165 | missense variant | G/A | snv | 1.7E-02 | 1.8E-02 | 98 | |
rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 82 | |
rs11209026 | 0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 | 46 | |
rs4986791 | 0.456 | 0.840 | 9 | 117713324 | missense variant | C/T | snv | 5.7E-02 | 4.9E-02 | 182 | |
rs61839660 | 0.776 | 0.280 | 10 | 6052734 | intron variant | C/T | snv | 5.7E-02 | 9 | ||
rs3134792 | 0.851 | 0.280 | 6 | 31344549 | intron variant | T/G | snv | 8.8E-02 | 4 | ||
rs1801282 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 131 | |
rs2295827 | 0.851 | 0.200 | 14 | 52708263 | intron variant | C/T | snv | 9.6E-02 | 9.1E-02 | 4 | |
rs2647044 | 0.882 | 0.240 | 6 | 32700133 | intergenic variant | G/A | snv | 0.10 | 3 | ||
rs2295826 | 0.851 | 0.200 | 14 | 52708205 | intron variant | A/G | snv | 0.11 | 4 | ||
rs1893217 | 0.742 | 0.440 | 18 | 12809341 | intron variant | A/G | snv | 0.12 | 14 | ||
rs1800629 | 0.472 | 0.920 | 6 | 31575254 | upstream gene variant | G/A | snv | 0.12 | 0.14 | 169 | |
rs4613763 | 0.851 | 0.240 | 5 | 40392626 | regulatory region variant | T/C | snv | 0.14 | 4 | ||
rs13222905 | 0.882 | 0.160 | 7 | 150566901 | upstream gene variant | G/A | snv | 0.15 | 3 | ||
rs7775228 | 0.790 | 0.360 | 6 | 32690302 | TF binding site variant | T/C | snv | 0.15 | 7 | ||
rs2327832 | 0.790 | 0.320 | 6 | 137651931 | intergenic variant | A/G | snv | 0.16 | 10 | ||
rs6534349 | 0.925 | 0.160 | 4 | 122481040 | intergenic variant | A/G | snv | 0.17 | 2 | ||
rs6965571 | 0.882 | 0.160 | 7 | 150737384 | 5 prime UTR variant | G/A | snv | 0.18 | 3 | ||
rs404860 | 0.925 | 0.160 | 6 | 32216568 | non coding transcript exon variant | T/C | snv | 0.21 | 2 | ||
rs1800566 | 0.576 | 0.680 | 16 | 69711242 | missense variant | G/A | snv | 0.25 | 0.21 | 59 | |
rs1131498 | 0.732 | 0.360 | 1 | 169707345 | missense variant | A/G | snv | 0.21 | 0.22 | 13 | |
rs2855812 | 0.790 | 0.360 | 6 | 31504943 | intron variant | G/T | snv | 0.23 | 13 | ||
rs12150079 | 0.807 | 0.280 | 17 | 39869164 | intron variant | G/A | snv | 0.24 | 9 |