Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10204525 | 0.701 | 0.440 | 2 | 241850169 | 3 prime UTR variant | C/T | snv | 0.21 | 20 | ||
rs1054690270 | 0.827 | 0.160 | 8 | 144505907 | frameshift variant | CT/- | delins | 5 | |||
rs10932029 | 0.827 | 0.200 | 2 | 203937045 | intron variant | T/A;C | snv | 5 | |||
rs11003123 | 0.827 | 0.200 | 10 | 52771774 | upstream gene variant | G/A | snv | 0.30 | 6 | ||
rs12304647 | 0.807 | 0.160 | 12 | 53991163 | intron variant | A/C | snv | 0.26 | 6 | ||
rs12979860 | 0.547 | 0.520 | 19 | 39248147 | intron variant | C/T | snv | 0.39 | 84 | ||
rs12980275 | 0.701 | 0.360 | 19 | 39241143 | upstream gene variant | A/G | snv | 0.36 | 23 | ||
rs13347 | 0.763 | 0.320 | 11 | 35231725 | 3 prime UTR variant | C/A;T | snv | 12 | |||
rs1358379 | 0.882 | 0.160 | 6 | 71403739 | intron variant | T/C | snv | 6.2E-02 | 3 | ||
rs1544410 | 0.542 | 0.760 | 12 | 47846052 | intron variant | C/A;G;T | snv | 78 | |||
rs187238 | 0.602 | 0.680 | 11 | 112164265 | intron variant | C/A;G | snv | 48 | |||
rs2275913 | 0.514 | 0.760 | 6 | 52186235 | upstream gene variant | G/A | snv | 0.28 | 105 | ||
rs2596542 | 0.724 | 0.200 | 6 | 31398818 | upstream gene variant | C/T | snv | 0.41 | 18 | ||
rs28934571 | 0.645 | 0.360 | 17 | 7674216 | missense variant | C/A;G | snv | 31 | |||
rs2896019 | 0.790 | 0.160 | 22 | 43937814 | intron variant | T/G | snv | 0.20 | 10 | ||
rs3077 | 0.701 | 0.440 | 6 | 33065245 | 3 prime UTR variant | A/G | snv | 0.29 | 16 | ||
rs3129859 | 0.827 | 0.320 | 6 | 32433162 | intergenic variant | G/C;T | snv | 5 | |||
rs3820998 | 0.882 | 0.120 | 2 | 161138615 | intron variant | C/A;T | snv | 3 | |||
rs4444903 | 0.630 | 0.360 | 4 | 109912954 | 5 prime UTR variant | A/G | snv | 0.51 | 35 | ||
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 | ||
rs510432 | 0.752 | 0.280 | 6 | 106326155 | upstream gene variant | T/C | snv | 0.57 | 11 | ||
rs548234 | 0.763 | 0.360 | 6 | 106120159 | intron variant | C/T | snv | 0.76 | 11 | ||
rs705382 | 0.827 | 0.200 | 7 | 95325909 | upstream gene variant | C/G | snv | 0.53 | 5 | ||
rs7536540 | 0.882 | 0.160 | 1 | 65058899 | intron variant | C/G;T | snv | 0.65 | 3 |