Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800872 | 0.495 | 0.840 | 1 | 206773062 | 5 prime UTR variant | T/G | snv | 0.69 | 119 | ||
rs20541 | 0.585 | 0.720 | 5 | 132660272 | missense variant | A/G | snv | 0.72 | 0.77 | 52 | |
rs2569190 | 0.620 | 0.560 | 5 | 140633331 | intron variant | A/G | snv | 0.57 | 39 | ||
rs1059513 | 0.776 | 0.240 | 12 | 57095926 | 3 prime UTR variant | T/C | snv | 8.0E-02 | 11 | ||
rs9275596 | 0.827 | 0.280 | 6 | 32713854 | upstream gene variant | C/T | snv | 0.66 | 7 | ||
rs7192 | 0.827 | 0.200 | 6 | 32443869 | missense variant | T/G | snv | 0.64 | 0.61 | 7 | |
rs1295686 | 0.882 | 0.160 | 5 | 132660151 | intron variant | T/A;C | snv | 0.68 | 7 | ||
rs324015 | 0.827 | 0.120 | 12 | 57096317 | 3 prime UTR variant | T/C | snv | 0.76 | 5 | ||
rs1343795 | 0.882 | 0.120 | 17 | 49334880 | intron variant | C/A | snv | 0.78 | 5 | ||
rs976078 | 0.882 | 0.120 | 13 | 82963398 | intron variant | A/C | snv | 0.15 | 4 | ||
rs4572450 | 0.882 | 0.120 | 17 | 49343367 | intron variant | T/C | snv | 0.78 | 4 | ||
rs4896888 | 1.000 | 0.040 | 6 | 146777855 | intron variant | C/T | snv | 0.47 | 2 | ||
rs1036504 | 1.000 | 0.040 | 7 | 2570131 | intron variant | C/T | snv | 0.61 | 2 | ||
rs2917750 | 1.000 | 0.040 | 7 | 2573790 | intron variant | T/G | snv | 0.57 | 2 | ||
rs4235235 | 1.000 | 0.040 | 4 | 154182301 | intron variant | C/T | snv | 0.83 | 1 | ||
rs9325071 | 1.000 | 0.040 | 5 | 148117775 | intron variant | A/G | snv | 0.22 | 1 |