Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6740847 | 0.925 | 0.040 | 2 | 181443625 | intergenic variant | A/G | snv | 0.57 | 8 | ||
rs1384936174 | 0.827 | 0.040 | 16 | 50710812 | missense variant | G/A;T | snv | 4.0E-06; 4.0E-06 | 6 | ||
rs4821544 | 0.925 | 0.040 | 22 | 36862461 | intron variant | T/A;C | snv | 6 | |||
rs11924265 | 1.000 | 0.040 | 3 | 65774667 | intron variant | T/C | snv | 7.5E-02 | 5 | ||
rs2076756 | 0.882 | 0.040 | 16 | 50722970 | intron variant | A/G | snv | 0.17 | 5 | ||
rs724016 | 1.000 | 0.040 | 3 | 141386728 | 5 prime UTR variant | A/G | snv | 0.52 | 5 | ||
rs11581607 | 0.925 | 0.040 | 1 | 67242007 | intron variant | G/A | snv | 4.6E-02 | 4 | ||
rs2066843 | 0.925 | 0.040 | 16 | 50711288 | synonymous variant | C/A;T | snv | 0.19 | 4 | ||
rs2297322 | 1.000 | 0.040 | 13 | 98723927 | missense variant | C/G;T | snv | 0.22 | 4 | ||
rs272879 | 0.882 | 0.040 | 5 | 132334853 | synonymous variant | C/A;G;T | snv | 4.0E-06; 0.57 | 4 | ||
rs3814055 | 0.925 | 0.040 | 3 | 119781188 | 5 prime UTR variant | C/T | snv | 0.35 | 4 | ||
rs3814057 | 0.925 | 0.040 | 3 | 119818407 | 3 prime UTR variant | A/C | snv | 0.28 | 4 | ||
rs7720838 | 0.925 | 0.040 | 5 | 40486794 | intron variant | G/T | snv | 0.52 | 4 | ||
rs962917 | 0.882 | 0.040 | 19 | 17191438 | intron variant | G/A | snv | 0.45 | 4 | ||
rs1049526 | 0.925 | 0.040 | 6 | 32981027 | 3 prime UTR variant | C/T | snv | 0.93 | 3 | ||
rs10761659 | 0.925 | 0.040 | 10 | 62685804 | intron variant | A/G | snv | 0.43 | 3 | ||
rs10781499 | 0.925 | 0.040 | 9 | 136371953 | synonymous variant | G/A | snv | 0.41 | 0.38 | 3 | |
rs11010067 | 0.925 | 0.040 | 10 | 35006503 | downstream gene variant | C/G | snv | 0.37 | 3 | ||
rs11190141 | 1.000 | 0.040 | 10 | 99532633 | upstream gene variant | C/T | snv | 0.40 | 3 | ||
rs113653754 | 0.925 | 0.040 | 6 | 32658495 | upstream gene variant | C/A | snv | 3 | |||
rs11641184 | 0.925 | 0.040 | 16 | 11610795 | intron variant | C/A | snv | 0.36 | 3 | ||
rs11741861 | 0.925 | 0.040 | 5 | 150898347 | intron variant | A/G | snv | 8.8E-02 | 3 | ||
rs11742570 | 0.925 | 0.040 | 5 | 40410482 | upstream gene variant | T/C;G | snv | 3 | |||
rs12103 | 0.925 | 0.040 | 1 | 1312114 | synonymous variant | T/A;C;G | snv | 0.56 | 3 | ||
rs1250569 | 0.925 | 0.040 | 10 | 79285450 | intron variant | T/C | snv | 0.44 | 0.51 | 3 |