Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1701704 | 0.851 | 0.200 | 12 | 56018703 | intron variant | T/G | snv | 0.25 | 5 | ||
rs2292239 | 0.742 | 0.480 | 12 | 56088396 | intron variant | T/G | snv | 0.65 | 4 | ||
rs1004446 | 0.827 | 0.240 | 11 | 2148913 | intron variant | G/A | snv | 0.37 | 3 | ||
rs3851179 | 0.752 | 0.280 | 11 | 86157598 | downstream gene variant | T/C | snv | 0.70 | 3 | ||
rs543293 | 0.925 | 0.080 | 11 | 86109035 | regulatory region variant | A/G | snv | 0.72 | 2 | ||
rs689 | 0.776 | 0.280 | 11 | 2160994 | splice region variant | A/T | snv | 0.73 | 0.60 | 1 | |
rs7941541 | 11 | 86147496 | intergenic variant | G/A | snv | 0.73 | 1 | ||||
rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 8 | |||
rs12722495 | 0.851 | 0.200 | 10 | 6055320 | intron variant | T/C | snv | 7.0E-02 | 1 | ||
rs657152 | 0.882 | 0.200 | 9 | 133263862 | intron variant | A/C;T | snv | 14 | |||
rs11136000 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 3 | ||
rs13266634 | 0.724 | 0.480 | 8 | 117172544 | missense variant | C/A;T | snv | 0.29 | 3 | ||
rs2582367 | 1.000 | 0.080 | 8 | 27622508 | regulatory region variant | C/T | snv | 0.64 | 2 | ||
rs11755527 | 0.851 | 0.360 | 6 | 90248512 | intron variant | C/G | snv | 0.36 | 3 | ||
rs4712523 | 0.925 | 0.120 | 6 | 20657333 | intron variant | A/G | snv | 0.41 | 3 | ||
rs12518099 | 0.925 | 0.120 | 5 | 90250292 | intron variant | A/G;T | snv | 3 | |||
rs4689388 | 0.882 | 0.360 | 4 | 6268329 | upstream gene variant | G/A | snv | 0.64 | 3 | ||
rs2069762 | 0.672 | 0.560 | 4 | 122456825 | upstream gene variant | A/C | snv | 0.24 | 1 | ||
rs3087243 | 0.623 | 0.720 | 2 | 203874196 | downstream gene variant | G/A | snv | 0.37 | 6 | ||
rs1990760 | 0.672 | 0.480 | 2 | 162267541 | missense variant | C/T | snv | 0.50 | 0.45 | 4 | |
rs2943641 | 0.763 | 0.160 | 2 | 226229029 | intergenic variant | T/C | snv | 0.67 | 3 | ||
rs11894266 | 1.000 | 0.080 | 2 | 169780132 | downstream gene variant | C/T | snv | 0.45 | 2 | ||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 13 | |
rs3024505 | 0.790 | 0.320 | 1 | 206766559 | upstream gene variant | G/A | snv | 0.11 | 6 | ||
rs7528684 | 0.752 | 0.560 | 1 | 157701026 | upstream gene variant | A/G | snv | 0.57 | 1 |