Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 187 | ||
rs1801275 | 0.581 | 0.680 | 16 | 27363079 | missense variant | A/G | snv | 0.25 | 0.36 | 58 | |
rs1051740 | 0.592 | 0.760 | 1 | 225831932 | missense variant | T/C | snv | 0.32 | 0.27 | 56 | |
rs3834129 | 0.627 | 0.560 | 2 | 201232809 | upstream gene variant | AGTAAG/- | del | 0.48 | 38 | ||
rs1045485 | 0.637 | 0.480 | 2 | 201284866 | missense variant | G/A;C;T | snv | 4.0E-06; 9.0E-02 | 34 | ||
rs3745274 | 0.672 | 0.480 | 19 | 41006936 | missense variant | G/A;T | snv | 4.0E-06; 0.27 | 30 | ||
rs5010528 | 0.827 | 0.240 | 6 | 31273255 | intron variant | A/G | snv | 0.15 | 9 | ||
rs4917014 | 0.807 | 0.360 | 7 | 50266267 | upstream gene variant | T/G | snv | 0.26 | 8 | ||
rs3815087 | 0.851 | 0.200 | 6 | 31125810 | 5 prime UTR variant | G/A | snv | 0.25 | 8 | ||
rs2779249 | 0.851 | 0.200 | 17 | 27801555 | intron variant | C/A | snv | 0.33 | 7 | ||
rs28399499 | 0.827 | 0.280 | 19 | 41012316 | missense variant | T/C | snv | 5.1E-03 | 2.2E-02 | 6 | |
rs9469003 | 0.882 | 0.160 | 6 | 31440051 | intron variant | T/C | snv | 0.22 | 6 | ||
rs3130501 | 0.851 | 0.280 | 6 | 31168676 | intron variant | A/G | snv | 0.78 | 4 | ||
rs2844665 | 0.882 | 0.200 | 6 | 31039078 | downstream gene variant | T/C | snv | 0.65 | 3 | ||
rs6500265 | 0.882 | 0.240 | 16 | 49912759 | intergenic variant | C/G;T | snv | 0.27 | 3 | ||
rs9933632 | 0.882 | 0.240 | 16 | 49906847 | intergenic variant | G/T | snv | 0.31 | 3 | ||
rs79908535 | 0.882 | 0.280 | 5 | 132679856 | missense variant | G/A | snv | 6.8E-05 | 2.8E-05 | 3 | |
rs41544623 | 0.882 | 0.280 | 6 | 31411083 | missense variant | C/T | snv | 3 | |||
rs3094188 | 0.882 | 0.200 | 6 | 31174468 | intron variant | C/A;T | snv | 0.68 | 3 | ||
rs2734583 | 0.882 | 0.240 | 6 | 31537703 | intron variant | A/G | snv | 0.10 | 3 | ||
rs6016348 | 0.925 | 0.160 | 20 | 40410188 | regulatory region variant | C/T | snv | 0.28 | 2 | ||
rs9888871 | 0.925 | 0.160 | 16 | 49916730 | downstream gene variant | G/C | snv | 0.19 | 2 | ||
rs384129 | 0.925 | 0.160 | 11 | 22670928 | intron variant | T/A | snv | 2 | |||
rs16957893 | 0.925 | 0.160 | 15 | 73437142 | intergenic variant | G/C | snv | 4.9E-02 | 2 |