Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17070145 | 0.790 | 0.120 | 5 | 168418786 | intron variant | C/T | snv | 0.43 | 10 | ||
rs140226130 | 0.790 | 0.200 | 18 | 33336845 | intron variant | -/CTTTTTGCT | delins | 7.8E-02 | 8 | ||
rs6656401 | 0.776 | 0.200 | 1 | 207518704 | intron variant | A/G;T | snv | 8 | |||
rs10163755 | 0.827 | 0.200 | 18 | 31405413 | intron variant | G/A | snv | 0.74 | 6 | ||
rs73069071 | 0.807 | 0.240 | 12 | 21357370 | intron variant | T/C | snv | 0.14 | 6 | ||
rs554521234 | 0.851 | 0.160 | 18 | 32231169 | intron variant | C/T | snv | 1.1E-02 | 4 | ||
rs970866 | 0.851 | 0.160 | 18 | 31681955 | intron variant | C/T | snv | 0.89 | 4 | ||
rs2949506 | 0.851 | 0.160 | 18 | 30217168 | intergenic variant | C/T | snv | 0.14 | 5 | ||
rs13031703 | 0.925 | 0.120 | 2 | 127129099 | intergenic variant | C/T | snv | 0.11 | 2 | ||
rs73956431 | 0.827 | 0.120 | 18 | 31699870 | regulatory region variant | C/T | snv | 8.4E-02 | 6 | ||
rs80356710 | 0.925 | 0.040 | 20 | 4699655 | stop gained | T/G | snv | 3 | |||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs61752717 | 0.583 | 0.840 | 16 | 3243407 | missense variant | T/A;C | snv | 2.8E-04 | 72 | ||
rs28933979 | 0.587 | 0.600 | 18 | 31592974 | missense variant | G/A;C | snv | 1.0E-04 | 70 | ||
rs121912438 | 0.605 | 0.520 | 21 | 31667299 | missense variant | G/A;C;T | snv | 1.2E-05; 8.0E-06 | 58 | ||
rs3743930 | 0.611 | 0.720 | 16 | 3254626 | missense variant | C/G;T | snv | 7.1E-02 | 43 | ||
rs76992529 | 0.653 | 0.560 | 18 | 31598655 | missense variant | G/A | snv | 1.1E-03 | 4.9E-03 | 36 | |
rs237025 | 0.672 | 0.360 | 6 | 149400554 | missense variant | G/A | snv | 0.55 | 0.57 | 26 | |
rs4149584 | 0.683 | 0.440 | 12 | 6333477 | missense variant | C/G;T | snv | 4.0E-06; 1.3E-02 | 24 | ||
rs63750231 | 0.689 | 0.160 | 14 | 73198100 | missense variant | A/C;G | snv | 23 | |||
rs1475170339 | 0.732 | 0.240 | 16 | 1792325 | missense variant | T/C;G | snv | 18 | |||
rs781049584 | 0.724 | 0.280 | 21 | 26021917 | missense variant | T/G | snv | 8.2E-06 | 7.0E-06 | 18 | |
rs28940580 | 0.742 | 0.560 | 16 | 3243447 | missense variant | C/A;G;T | snv | 1.0E-04; 8.0E-06 | 17 | ||
rs267607161 | 0.742 | 0.360 | 18 | 31598580 | missense variant | G/T | snv | 4.0E-06 | 7.0E-06 | 16 |