Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 83 | ||
rs1360780 | 0.708 | 0.320 | 6 | 35639794 | intron variant | T/A;C | snv | 31 | |||
rs3745274 | 0.672 | 0.480 | 19 | 41006936 | missense variant | G/A;T | snv | 4.0E-06; 0.27 | 30 | ||
rs2853676 | 0.667 | 0.560 | 5 | 1288432 | intron variant | T/A;C | snv | 29 | |||
rs698 | 0.724 | 0.240 | 4 | 99339632 | missense variant | T/A;C | snv | 0.35 | 20 | ||
rs1044396 | 0.742 | 0.240 | 20 | 63349782 | missense variant | G/A;C | snv | 0.47; 6.1E-05 | 17 | ||
rs27072 | 0.807 | 0.120 | 5 | 1394407 | 3 prime UTR variant | C/A;T | snv | 11 | |||
rs1137070 | 0.763 | 0.160 | X | 43744144 | synonymous variant | T/C | snv | 0.62 | 9 | ||
rs686 | 0.807 | 0.080 | 5 | 175441697 | 3 prime UTR variant | G/A;C;T | snv | 9 | |||
rs130058 | 0.790 | 0.120 | 6 | 77463564 | 5 prime UTR variant | T/A;G | snv | 8 | |||
rs1800955 | 0.827 | 0.160 | 11 | 636784 | upstream gene variant | T/C;G | snv | 8 | |||
rs2279343 | 0.776 | 0.200 | 19 | 41009358 | missense variant | A/G | snv | 0.13 | 8 | ||
rs28399433 | 0.827 | 0.200 | 19 | 40850474 | intron variant | A/C;G;T | snv | 0.10; 4.4E-06 | 7 | ||
rs4105144 | 0.827 | 0.160 | 19 | 40852719 | intron variant | T/C | snv | 7 | |||
rs1329650 | 0.882 | 0.080 | 10 | 91588363 | regulatory region variant | G/A;T | snv | 6 | |||
rs588765 | 0.827 | 0.200 | 15 | 78573083 | intron variant | T/A;C | snv | 6 | |||
rs1948 | 0.827 | 0.160 | 15 | 78625057 | synonymous variant | A/G;T | snv | 0.69 | 5 | ||
rs2653349 | 0.882 | 0.120 | 6 | 55277539 | missense variant | A/G;T | snv | 0.84; 4.0E-06 | 5 | ||
rs9332377 | 0.882 | 0.120 | 22 | 19968169 | intron variant | C/A;T | snv | 5 | |||
rs660652 | 1.000 | 0.080 | 15 | 78595490 | 3 prime UTR variant | A/G;T | snv | 3 | |||
rs68081839 | 0.882 | 0.080 | 11 | 105762027 | intron variant | TT/-;T;TTT;TTTT;TTTTT;TTTTTTTTTTTT | delins | 3 | |||
rs72552266 | 0.882 | 0.200 | 19 | 41089049 | stop gained | C/G;T | snv | 4.0E-06; 5.8E-03 | 3 | ||
rs8192789 | 1.000 | 0.080 | 19 | 41091846 | missense variant | C/A;T | snv | 4.0E-06; 3.1E-02 | 3 | ||
rs9217 | 1.000 | 0.080 | 17 | 7459769 | 3 prime UTR variant | T/A;C | snv | 3 |