Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
rs1799971 | 0.559 | 0.600 | 6 | 154039662 | missense variant | A/G | snv | 0.19 | 0.12 | 95 | |
rs17576 | 0.557 | 0.760 | 20 | 46011586 | missense variant | A/G | snv | 0.39 | 0.36 | 73 | |
rs4633 | 0.695 | 0.400 | 22 | 19962712 | synonymous variant | C/T | snv | 0.46 | 0.45 | 25 | |
rs8040868 | 0.742 | 0.240 | 15 | 78618839 | synonymous variant | T/C | snv | 0.35 | 0.37 | 17 | |
rs143383 | 0.724 | 0.320 | 20 | 35438203 | 5 prime UTR variant | G/A | snv | 0.47 | 17 | ||
rs10767664 | 0.752 | 0.400 | 11 | 27704439 | intron variant | T/A | snv | 0.83 | 16 | ||
rs11030104 | 0.790 | 0.240 | 11 | 27662970 | intron variant | A/G | snv | 0.16 | 12 | ||
rs886205 | 0.827 | 0.360 | 12 | 111766623 | intron variant | A/G | snv | 0.35 | 8 | ||
rs1676486 | 0.851 | 0.120 | 1 | 102888582 | missense variant | A/G;T | snv | 0.80; 4.0E-06 | 7 | ||
rs10490571 | 0.827 | 0.320 | 2 | 102100877 | intron variant | C/T | snv | 0.29 | 5 | ||
rs11030096 | 0.925 | 0.160 | 11 | 27643996 | intron variant | T/A;C | snv | 3 | |||
rs2615977 | 0.925 | 0.080 | 1 | 102986836 | intron variant | A/C | snv | 0.27 | 3 | ||
rs11066028 | 1.000 | 0.080 | 12 | 111807366 | intron variant | A/C | snv | 0.45 | 2 | ||
rs7296651 | 0.925 | 0.160 | 12 | 111809150 | intron variant | C/A;G | snv | 2 | |||
rs7481311 | 0.925 | 0.160 | 11 | 27561582 | intron variant | T/C | snv | 0.75 | 2 | ||
rs956730 | 0.925 | 0.120 | 2 | 102141656 | intron variant | G/A | snv | 0.42 | 2 | ||
rs375081888 | 0.925 | 0.120 | 12 | 117331048 | missense variant | C/T | snv | 2.4E-05 | 7.0E-06 | 2 | |
rs9406328 | 1.000 | 0.080 | 6 | 169234915 | splice region variant | G/A | snv | 0.37 | 0.31 | 2 | |
rs11030064 | 1.000 | 0.080 | 11 | 27596469 | intron variant | C/T | snv | 0.41 | 1 | ||
rs62413038 | 1.000 | 0.080 | 6 | 63952008 | intron variant | T/A;G | snv | 0.49 | 1 | ||
rs9450607 | 1.000 | 0.080 | 6 | 64025138 | intron variant | A/G | snv | 0.32 | 1 | ||
rs6651255 | 1.000 | 0.080 | 8 | 129711546 | intron variant | T/A;C | snv | 1 |