Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 174 | |
rs5744174 | 0.742 | 0.360 | 1 | 223111186 | missense variant | A/G | snv | 0.39 | 0.34 | 13 | |
rs3024490 | 0.742 | 0.520 | 1 | 206771966 | intron variant | A/C;G;T | snv | 11 | |||
rs3093059 | 0.752 | 0.520 | 1 | 159715346 | upstream gene variant | A/G | snv | 0.13 | 11 | ||
rs3754093 | 0.776 | 0.240 | 1 | 241846814 | upstream gene variant | A/G | snv | 0.23 | 11 | ||
rs636832 | 0.790 | 0.400 | 1 | 35897874 | intron variant | G/A | snv | 0.23 | 8 | ||
rs17401966 | 0.790 | 0.280 | 1 | 10325413 | intron variant | A/G | snv | 0.24 | 7 | ||
rs2070150 | 0.827 | 0.280 | 1 | 161791486 | missense variant | G/C | snv | 0.14 | 9.2E-02 | 6 | |
rs11465817 | 0.882 | 0.120 | 1 | 67255414 | intron variant | C/A;T | snv | 4 | |||
rs4649203 | 0.851 | 0.160 | 1 | 24193430 | intergenic variant | G/A | snv | 0.61 | 4 | ||
rs4656942 | 0.851 | 0.160 | 1 | 160861258 | intron variant | G/A;C;T | snv | 4 | |||
rs485618 | 0.851 | 0.160 | 1 | 160830690 | 3 prime UTR variant | T/A;C;G | snv | 0.54 | 4 | ||
rs7536540 | 0.882 | 0.160 | 1 | 65058899 | intron variant | C/G;T | snv | 0.65 | 3 | ||
rs7549785 | 0.925 | 0.080 | 1 | 159308078 | 3 prime UTR variant | G/A | snv | 0.13 | 3 | ||
rs10918706 | 0.925 | 0.200 | 1 | 167496884 | intron variant | C/T | snv | 0.24 | 2 | ||
rs12133337 | 0.925 | 0.160 | 1 | 167483453 | intron variant | T/C | snv | 0.17 | 2 | ||
rs1329044438 | 0.925 | 0.120 | 1 | 53906244 | missense variant | G/A | snv | 2 | |||
rs17127024 | 0.925 | 0.280 | 1 | 64837448 | intron variant | G/T | snv | 5.1E-02 | 2 | ||
rs10912564 | 1.000 | 0.080 | 1 | 173201479 | intron variant | C/T | snv | 0.43 | 1 | ||
rs4244165 | 1.000 | 0.080 | 1 | 64955388 | intron variant | G/C;T | snv | 1 | |||
rs7525481 | 1.000 | 0.080 | 1 | 24154900 | 3 prime UTR variant | C/T | snv | 0.54 | 1 | ||
rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 | ||
rs16944 | 0.531 | 0.920 | 2 | 112837290 | upstream gene variant | A/G | snv | 0.57 | 92 |