Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7574865 | 0.574 | 0.720 | 2 | 191099907 | intron variant | T/G | snv | 0.79 | 9 | ||
rs1883832 | 0.581 | 0.680 | 20 | 46118343 | 5 prime UTR variant | T/C | snv | 0.75 | 0.80 | 7 | |
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 5 | |
rs3761959 | 0.827 | 0.320 | 1 | 157699488 | intron variant | C/A;G;T | snv | 4 | |||
rs6074022 | 0.851 | 0.240 | 20 | 46111557 | TF binding site variant | C/G;T | snv | 3 | |||
rs4810485 | 0.732 | 0.480 | 20 | 46119308 | intron variant | T/A;G | snv | 3 | |||
rs1800693 | 0.776 | 0.360 | 12 | 6330843 | non coding transcript exon variant | T/C | snv | 0.36; 4.0E-06 | 0.38 | 3 | |
rs6897932 | 0.683 | 0.560 | 5 | 35874473 | missense variant | C/T | snv | 0.23 | 0.21 | 2 | |
rs704840 | 0.851 | 0.240 | 1 | 173257056 | intergenic variant | T/G | snv | 0.29 | 2 | ||
rs2300747 | 0.882 | 0.200 | 1 | 116561593 | intron variant | A/G | snv | 0.19 | 2 | ||
rs10168266 | 0.776 | 0.400 | 2 | 191071078 | intron variant | C/T | snv | 0.19 | 2 | ||
rs7601754 | 0.882 | 0.160 | 2 | 191075725 | intron variant | G/A;T | snv | 2 | |||
rs4149577 | 0.827 | 0.280 | 12 | 6338356 | intron variant | G/A;T | snv | 2 | |||
rs1150757 | 0.925 | 0.160 | 6 | 32061428 | synonymous variant | G/A;C | snv | 5.9E-02 | 2 | ||
rs28383224 | 0.925 | 0.160 | 6 | 32615876 | regulatory region variant | A/G | snv | 0.55 | 1 | ||
rs73366469 | 0.925 | 0.160 | 7 | 74619286 | regulatory region variant | T/C | snv | 0.12 | 1 | ||
rs548234 | 0.763 | 0.360 | 6 | 106120159 | intron variant | C/T | snv | 0.76 | 1 | ||
rs3135388 | 0.807 | 0.240 | 6 | 32445274 | downstream gene variant | A/G | snv | 0.90 | 1 | ||
rs763780 | 0.531 | 0.720 | 6 | 52236941 | missense variant | T/C | snv | 6.7E-02 | 6.6E-02 | 1 | |
rs117026326 | 0.752 | 0.440 | 7 | 74711703 | intron variant | C/T | snv | 1.3E-02 | 1 | ||
rs9523762 | 0.925 | 0.120 | 13 | 92679633 | intron variant | G/A | snv | 0.39 | 1 | ||
rs703842 | 0.851 | 0.240 | 12 | 57768956 | missense variant | A/G | snv | 0.38 | 0.33 | 1 | |
rs422951 | 0.807 | 0.280 | 6 | 32220606 | missense variant | T/C | snv | 0.40 | 0.40 | 1 | |
rs1520333 | 0.925 | 0.120 | 8 | 78488803 | intron variant | A/G | snv | 0.40 | 1 | ||
rs10181656 | 0.763 | 0.360 | 2 | 191105153 | intron variant | G/C | snv | 0.79 | 1 |