Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7746082 | 0.851 | 0.160 | 6 | 105987394 | regulatory region variant | G/A;C | snv | 3 | |||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 13 | |
rs4263839 | 0.807 | 0.160 | 9 | 114804160 | intron variant | A/G | snv | 0.75 | 3 | ||
rs1551398 | 0.882 | 0.160 | 8 | 125527809 | intron variant | G/A | snv | 0.48 | 3 | ||
rs2542151 | 0.763 | 0.480 | 18 | 12779948 | upstream gene variant | G/T | snv | 0.83 | 6 | ||
rs1893217 | 0.742 | 0.440 | 18 | 12809341 | intron variant | A/G | snv | 0.12 | 8 | ||
rs2188962 | 0.882 | 0.160 | 5 | 132435113 | intron variant | C/T | snv | 0.29 | 4 | ||
rs11167764 | 0.925 | 0.120 | 5 | 142099500 | regulatory region variant | A/C | snv | 0.80 | 2 | ||
rs11747270 | 0.790 | 0.240 | 5 | 150879305 | intron variant | A/G | snv | 0.21 | 3 | ||
rs1736135 | 0.851 | 0.160 | 21 | 15432901 | intron variant | T/C | snv | 0.33 | 4 | ||
rs10045431 | 0.851 | 0.240 | 5 | 159387525 | intron variant | A/C | snv | 0.78 | 3 | ||
rs2274910 | 0.827 | 0.200 | 1 | 160882256 | non coding transcript exon variant | T/C | snv | 0.65 | 0.58 | 3 | |
rs2301436 | 0.752 | 0.320 | 6 | 167024500 | intron variant | C/T | snv | 0.42 | 4 | ||
rs9286879 | 0.851 | 0.200 | 1 | 172893094 | intron variant | A/G | snv | 0.32 | 4 | ||
rs11584383 | 0.827 | 0.200 | 1 | 200966738 | downstream gene variant | T/C | snv | 0.24 | 4 | ||
rs6908425 | 0.752 | 0.320 | 6 | 20728500 | intron variant | T/C | snv | 0.78 | 3 | ||
rs3828309 | 0.882 | 0.160 | 2 | 233271764 | intron variant | A/G | snv | 0.42 | 3 | ||
rs17582416 | 0.882 | 0.160 | 10 | 34998722 | regulatory region variant | T/G | snv | 0.31 | 3 | ||
rs2872507 | 0.752 | 0.360 | 17 | 39884510 | intergenic variant | G/A;T | snv | 7 | |||
rs11175593 | 0.882 | 0.160 | 12 | 40208138 | non coding transcript exon variant | C/T | snv | 2.8E-02 | 3 | ||
rs4613763 | 0.851 | 0.240 | 5 | 40392626 | regulatory region variant | T/C | snv | 0.14 | 3 | ||
rs744166 | 0.689 | 0.560 | 17 | 42362183 | intron variant | A/G | snv | 0.48 | 3 | ||
rs3764147 | 0.807 | 0.280 | 13 | 43883789 | missense variant | A/G | snv | 0.28 | 0.27 | 4 | |
rs762421 | 0.851 | 0.360 | 21 | 44195678 | intron variant | G/A | snv | 3 | |||
rs3197999 | 0.732 | 0.280 | 3 | 49684099 | missense variant | G/A | snv | 0.26 | 0.27 | 6 |