Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519975 | 0.649 | 0.480 | 17 | 7675209 | missense variant | A/C;G;T | snv | 13 | |||
rs2239633 | 0.742 | 0.240 | 14 | 23119848 | upstream gene variant | G/A | snv | 0.38 | 4 | ||
rs4132601 | 0.763 | 0.240 | 7 | 50402906 | 3 prime UTR variant | T/G | snv | 0.25 | 4 | ||
rs7089424 | 0.752 | 0.200 | 10 | 61992400 | intron variant | T/G | snv | 0.32 | 3 | ||
rs3824662 | 0.752 | 0.320 | 10 | 8062245 | intron variant | C/A;T | snv | 2 | |||
rs189434316 | 0.925 | 0.120 | 14 | 92231568 | intergenic variant | A/T | snv | 4.1E-02 | 1 | ||
rs7090445 | 0.925 | 0.120 | 10 | 61961417 | intron variant | C/G;T | snv | 0.70 | 1 | ||
rs28665337 | 1.000 | 0.120 | 8 | 129181858 | intron variant | C/A;T | snv | 1 | |||
rs3731217 | 0.763 | 0.320 | 9 | 21984662 | intron variant | A/C;T | snv | 1 | |||
rs3731249 | 0.683 | 0.320 | 9 | 21970917 | missense variant | C/A;G;T | snv | 2.1E-02 | 1 | ||
rs4762284 | 1.000 | 0.120 | 12 | 96218984 | intron variant | A/T | snv | 0.36 | 1 | ||
rs11980379 | 0.882 | 0.120 | 7 | 50402283 | 3 prime UTR variant | T/C | snv | 0.25 | 1 | ||
rs35837782 | 0.925 | 0.120 | 10 | 124604740 | intron variant | A/G | snv | 0.63 | 1 | ||
rs10828317 | 0.776 | 0.280 | 10 | 22550699 | missense variant | T/C | snv | 1 |