Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10811474 | 0.742 | 0.240 | 9 | 21114238 | intergenic variant | A/G | snv | 0.44 | 11 | ||
rs1805105 | 0.776 | 0.280 | 16 | 346264 | synonymous variant | A/G | snv | 0.61 | 0.69 | 11 | |
rs12628 | 0.776 | 0.160 | 11 | 534242 | synonymous variant | A/G | snv | 0.32 | 0.34 | 10 | |
rs3731239 | 0.763 | 0.240 | 9 | 21974219 | intron variant | A/G | snv | 0.26 | 10 | ||
rs709816 | 0.752 | 0.320 | 8 | 89955483 | synonymous variant | A/G | snv | 0.47 | 0.51 | 10 | |
rs11191454 | 0.776 | 0.160 | 10 | 102900247 | intron variant | A/G | snv | 7.9E-02 | 9 | ||
rs9288518 | 0.776 | 0.240 | 2 | 216196997 | intron variant | A/G | snv | 0.35 | 9 | ||
rs1883965 | 0.807 | 0.160 | 1 | 11262099 | intron variant | A/G | snv | 0.63 | 8 | ||
rs8679 | 0.790 | 0.200 | 1 | 226360853 | 3 prime UTR variant | A/G | snv | 0.16 | 7 | ||
rs778990691 | 0.807 | 0.240 | 5 | 87395069 | missense variant | A/G | snv | 4.0E-06 | 6 | ||
rs7211818 | 0.827 | 0.200 | 17 | 80715103 | intron variant | A/G | snv | 0.23 | 5 | ||
rs1484761909 | 0.882 | 0.120 | 1 | 109688224 | missense variant | A/G | snv | 3.0E-05 | 3.8E-05 | 3 | |
rs6464268 | 0.882 | 0.120 | 7 | 152684065 | intergenic variant | A/G | snv | 0.23 | 3 | ||
rs121913279 | 0.526 | 0.560 | 3 | 179234297 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 101 | ||
rs2234922 | 0.630 | 0.440 | 1 | 225838705 | missense variant | A/G;T | snv | 0.19; 2.8E-05 | 42 | ||
rs156697 | 0.672 | 0.560 | 10 | 104279427 | missense variant | A/G;T | snv | 0.35 | 25 | ||
rs10719 | 0.677 | 0.680 | 5 | 31401340 | 3 prime UTR variant | A/G;T | snv | 0.69 | 24 | ||
rs2306283 | 0.742 | 0.320 | 12 | 21176804 | missense variant | A/G;T | snv | 0.47 | 16 | ||
rs2230641 | 0.807 | 0.240 | 5 | 87399457 | missense variant | A/G;T | snv | 0.18 | 0.17 | 8 | |
rs9034 | 0.827 | 0.200 | 7 | 106249610 | 3 prime UTR variant | A/G;T | snv | 5 | |||
rs1135612 | 0.882 | 0.120 | 7 | 75980359 | synonymous variant | A/G;T | snv | 0.28 | 3 | ||
rs140241283 | 0.882 | 0.120 | 1 | 11796249 | start lost | A/G;T | snv | 4.0E-06; 4.0E-06 | 3 | ||
rs1326656542 | 0.776 | 0.280 | 13 | 108210293 | missense variant | A/T | snv | 4.0E-06 | 10 | ||
rs760805 | 0.776 | 0.240 | 1 | 24925432 | intron variant | A/T | snv | 0.42 | 9 | ||
rs1547651 | 0.851 | 0.200 | 6 | 43762907 | regulatory region variant | A/T | snv | 0.15 | 4 |