Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs67164370 | 0.851 | 0.120 | 20 | 4787830 | intron variant | -/AGGGACT | ins | 4 | |||
rs3783553 | 0.667 | 0.480 | 2 | 112774138 | 3 prime UTR variant | -/TGAA | delins | 26 | |||
rs144848 | 0.653 | 0.440 | 13 | 32332592 | missense variant | A/C | snv | 0.28 | 0.23 | 29 | |
rs61764370 | 0.662 | 0.320 | 12 | 25207290 | 3 prime UTR variant | A/C | snv | 6.2E-02 | 29 | ||
rs314276 | 0.807 | 0.280 | 6 | 104960124 | intron variant | A/C | snv | 0.65 | 10 | ||
rs4987208 | 0.851 | 0.160 | 12 | 913403 | stop gained | A/C | snv | 3.5E-02 | 2.1E-02 | 4 | |
rs2256787 | 0.925 | 0.120 | 1 | 17566321 | intron variant | A/C | snv | 0.93 | 2 | ||
rs115344852 | 1.000 | 0.120 | 6 | 28518321 | intron variant | A/C | snv | 1 | |||
rs1614627 | 1.000 | 0.120 | 1 | 20620263 | downstream gene variant | A/C | snv | 0.86 | 1 | ||
rs854560 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 113 | ||
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
rs2072590 | 0.851 | 0.120 | 2 | 176177905 | non coding transcript exon variant | A/C;T | snv | 4 | |||
rs17329882 | 0.925 | 0.120 | 4 | 119028805 | intron variant | A/C;T | snv | 2 | |||
rs76032516 | 0.925 | 0.120 | 11 | 96097550 | intron variant | A/C;T | snv | 2 | |||
rs1695 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 188 | |
rs5498 | 0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 | 99 | |
rs1128503 | 0.564 | 0.760 | 7 | 87550285 | synonymous variant | A/G | snv | 0.54 | 0.63 | 64 | |
rs768623239 | 0.662 | 0.640 | 1 | 109689278 | missense variant | A/G | snv | 1.5E-05 | 26 | ||
rs851797 | 0.752 | 0.240 | 1 | 241889740 | 3 prime UTR variant | A/G | snv | 0.72 | 13 | ||
rs2070074 | 0.742 | 0.360 | 9 | 34649445 | missense variant | A/G | snv | 9.2E-02 | 7.4E-02 | 12 | |
rs17401966 | 0.790 | 0.280 | 1 | 10325413 | intron variant | A/G | snv | 0.24 | 7 | ||
rs11782652 | 0.851 | 0.120 | 8 | 81741409 | intron variant | A/G | snv | 6.6E-02 | 4 | ||
rs9303542 | 0.882 | 0.120 | 17 | 48334138 | intron variant | A/G | snv | 0.34 | 3 | ||
rs1057156 | 0.925 | 0.120 | 3 | 128081228 | 3 prime UTR variant | A/G | snv | 0.22 | 0.23 | 2 |