Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs771306418 | 0.851 | 0.120 | 3 | 9765885 | splice acceptor variant | -/C | delins | 5 | |||
rs3813034 | 0.827 | 0.160 | 17 | 30197786 | 3 prime UTR variant | A/C | snv | 0.40 | 8 | ||
rs2296972 | 0.925 | 0.080 | 13 | 46854336 | intron variant | A/C | snv | 0.70 | 4 | ||
rs11060369 | 1.000 | 0.040 | 12 | 129475652 | intron variant | A/C | snv | 0.41 | 1 | ||
rs8076112 | 1.000 | 0.040 | 17 | 1708905 | intron variant | A/C;G | snv | 0.15 | 1 | ||
rs11030104 | 0.790 | 0.240 | 11 | 27662970 | intron variant | A/G | snv | 0.16 | 12 | ||
rs2271933 | 0.807 | 0.080 | 1 | 31626924 | missense variant | A/G | snv | 0.56 | 0.50 | 9 | |
rs1800857 | 0.851 | 0.120 | 4 | 26489489 | splice region variant | A/G | snv | 0.17 | 0.18 | 4 | |
rs173365 | 0.882 | 0.080 | 17 | 45823708 | intron variant | A/G | snv | 0.55 | 3 | ||
rs17035816 | 0.925 | 0.040 | 4 | 157167312 | intron variant | A/G | snv | 0.11 | 2 | ||
rs1799923 | 0.925 | 0.040 | 3 | 42264802 | 5 prime UTR variant | A/G | snv | 0.82 | 2 | ||
rs10415555 | 1.000 | 0.040 | 19 | 33519283 | intron variant | A/G | snv | 0.19 | 1 | ||
rs10879357 | 1.000 | 0.040 | 12 | 72020783 | intron variant | A/G | snv | 0.59 | 1 | ||
rs12061304 | 1.000 | 0.040 | 1 | 110695063 | intergenic variant | A/G | snv | 0.30 | 1 | ||
rs191260602 | 1.000 | 0.040 | 4 | 157140489 | intron variant | A/G | snv | 7.7E-03 | 1 | ||
rs3742278 | 1.000 | 0.040 | 13 | 46845442 | intron variant | A/G | snv | 0.19 | 1 | ||
rs4583306 | 1.000 | 0.040 | 17 | 30211697 | intron variant | A/G | snv | 0.37 | 1 | ||
rs1800855 | 0.925 | 0.120 | 4 | 26489495 | intron variant | A/G;T | snv | 0.27 | 2 | ||
rs1418688 | 1.000 | 0.040 | 6 | 71169166 | downstream gene variant | A/G;T | snv | 1 | |||
rs4804833 | 1.000 | 0.040 | 19 | 7905750 | intron variant | A/G;T | snv | 1 | |||
rs4977831 | 1.000 | 0.040 | 9 | 20713069 | intron variant | A/G;T | snv | 1 | |||
rs324981 | 0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 | 18 | |
rs1326656542 | 0.776 | 0.280 | 13 | 108210293 | missense variant | A/T | snv | 4.0E-06 | 10 | ||
rs11179000 | 0.925 | 0.040 | 12 | 71944848 | intron variant | A/T | snv | 0.31 | 2 | ||
rs10801152 | 1.000 | 0.040 | 1 | 192792174 | intron variant | A/T | snv | 0.31 | 1 |