Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800896 | 0.507 | 0.800 | 1 | 206773552 | intron variant | T/C | snv | 0.41 | 113 | ||
rs3024490 | 0.742 | 0.520 | 1 | 206771966 | intron variant | A/C;G;T | snv | 11 | |||
rs1518111 | 0.790 | 0.360 | 1 | 206771300 | intron variant | T/C | snv | 0.71 | 9 | ||
rs3024493 | 0.776 | 0.280 | 1 | 206770623 | intron variant | C/A;T | snv | 0.11 | 9 | ||
rs3021094 | 0.827 | 0.360 | 1 | 206771607 | intron variant | T/G | snv | 8.0E-02 | 8 | ||
rs1518110 | 0.851 | 0.160 | 1 | 206771516 | intron variant | A/C;T | snv | 5 | |||
rs2222202 | 0.827 | 0.160 | 1 | 206772036 | intron variant | G/A | snv | 0.39 | 5 | ||
rs1878672 | 0.882 | 0.080 | 1 | 206770368 | intron variant | G/A;C;T | snv | 3 | |||
rs3790622 | 0.882 | 0.320 | 1 | 206771818 | intron variant | G/A | snv | 1.5E-03 | 3 | ||
rs3024491 | 0.925 | 0.040 | 1 | 206771701 | intron variant | C/A;T | snv | 2 | |||
rs1800893 | 1.000 | 0.120 | 1 | 206773822 | intron variant | C/T | snv | 0.41 | 1 | ||
rs3024495 | 1.000 | 0.080 | 1 | 206769068 | intron variant | C/A;T | snv | 1 | |||
rs1373589952 | 1.000 | 0.120 | 1 | 206772296 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
rs145922845 | 1.000 | 0.040 | 1 | 206772393 | missense variant | C/T | snv | 1.9E-03 | 1.8E-03 | 1 | |
rs1800872 | 0.495 | 0.840 | 1 | 206773062 | 5 prime UTR variant | T/G | snv | 0.69 | 119 | ||
rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 108 | ||
rs3021097 | 0.752 | 0.440 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 10 | |||
rs1554286 | 0.790 | 0.320 | 1 | 206770888 | 5 prime UTR variant | A/G;T | snv | 0.72 | 7 | ||
rs3024492 | 1 | 206770767 | 5 prime UTR variant | T/A | snv | 0.17 | 1 | ||||
rs3024498 | 0.790 | 0.360 | 1 | 206768184 | 3 prime UTR variant | T/C | snv | 0.20 | 7 | ||
rs3024496 | 0.827 | 0.200 | 1 | 206768519 | 3 prime UTR variant | A/G | snv | 0.43 | 6 |