Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs738408 | 0.925 | 0.120 | 22 | 43928850 | synonymous variant | C/T | snv | 0.28 | 0.22 | 10 | |
rs1057519753 | 0.763 | 0.120 | 1 | 64846664 | missense variant | C/A | snv | 9 | |||
rs12748152 | 1.000 | 0.120 | 1 | 26811902 | upstream gene variant | C/T | snv | 5.7E-02 | 8 | ||
rs1966862 | 0.790 | 0.120 | 4 | 85766908 | intron variant | A/G | snv | 0.14 | 8 | ||
rs10994982 | 0.790 | 0.120 | 10 | 61950345 | intron variant | A/G | snv | 0.49 | 7 | ||
rs121913488 | 0.807 | 0.120 | 13 | 28018505 | missense variant | C/A;G;T | snv | 7 | |||
rs924607 | 0.851 | 0.120 | 5 | 609978 | intron variant | C/T | snv | 0.32 | 7 | ||
rs387906517 | 0.827 | 0.120 | 9 | 130862919 | missense variant | G/A | snv | 6 | |||
rs121913448 | 0.827 | 0.120 | 9 | 130862976 | missense variant | G/A | snv | 5 | |||
rs6021191 | 0.851 | 0.120 | 20 | 51419700 | intron variant | A/T | snv | 4.9E-02 | 5 | ||
rs17007695 | 0.851 | 0.120 | 4 | 141788570 | intergenic variant | T/C | snv | 7.7E-02 | 4 | ||
rs186364861 | 0.882 | 0.120 | 13 | 48037798 | missense variant | G/A | snv | 9.1E-04 | 2.4E-04 | 4 | |
rs2274407 | 0.882 | 0.120 | 13 | 95206781 | missense variant | C/A;G;T | snv | 9.7E-02 | 0.10 | 4 | |
rs4748793 | 0.851 | 0.120 | 10 | 22194082 | intergenic variant | A/G | snv | 0.18 | 4 | ||
rs6964969 | 0.851 | 0.120 | 7 | 50405553 | downstream gene variant | A/G | snv | 0.23 | 4 | ||
rs7073837 | 0.851 | 0.120 | 10 | 61940136 | intron variant | A/C | snv | 0.58 | 0.64 | 4 | |
rs7088318 | 0.851 | 0.120 | 10 | 22564019 | intron variant | C/A | snv | 0.55 | 4 | ||
rs121909646 | 0.882 | 0.120 | 13 | 28018504 | missense variant | T/A;G | snv | 3 | |||
rs12669559 | 1.000 | 0.120 | 7 | 50368079 | synonymous variant | T/G | snv | 0.35 | 0.32 | 3 | |
rs12786200 | 1.000 | 0.120 | 11 | 92245852 | intergenic variant | C/T | snv | 0.22 | 3 | ||
rs144104656 | 1.000 | 0.120 | 2 | 118661291 | regulatory region variant | A/G | snv | 1.1E-03 | 3 | ||
rs147481775 | 1.000 | 0.120 | 22 | 31829377 | intron variant | C/A | snv | 6.6E-03 | 3 | ||
rs149940960 | 1.000 | 0.120 | 2 | 11641492 | 3 prime UTR variant | T/C | snv | 1.0E-02 | 3 | ||
rs17032980 | 1.000 | 0.120 | 2 | 67075611 | intergenic variant | A/G | snv | 0.25 | 3 | ||
rs34531324 | 1.000 | 0.120 | 5 | 174435441 | intron variant | A/T | snv | 0.16 | 3 |