Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2275913 | 0.514 | 0.760 | 6 | 52186235 | upstream gene variant | G/A | snv | 0.28 | 105 | ||
rs2327832 | 0.790 | 0.320 | 6 | 137651931 | intergenic variant | A/G | snv | 0.16 | 10 | ||
rs2488457 | 0.763 | 0.480 | 1 | 113872746 | intron variant | G/A;C | snv | 11 | |||
rs26232 | 0.925 | 0.160 | 5 | 103261019 | intron variant | C/T | snv | 0.30 | 4 | ||
rs2736340 | 0.683 | 0.480 | 8 | 11486464 | upstream gene variant | C/T | snv | 0.25 | 22 | ||
rs28362491 | 0.592 | 0.720 | 4 | 102500998 | non coding transcript exon variant | ATTG/- | delins | 56 | |||
rs3027898 | 0.752 | 0.360 | X | 154010439 | downstream gene variant | C/A | snv | 11 | |||
rs3087243 | 0.623 | 0.720 | 2 | 203874196 | downstream gene variant | G/A | snv | 0.37 | 44 | ||
rs3087456 | 0.742 | 0.480 | 16 | 10877045 | intron variant | G/A | snv | 0.53 | 14 | ||
rs3093023 | 0.851 | 0.160 | 6 | 167120802 | intron variant | G/A | snv | 0.34 | 7 | ||
rs3212227 | 0.566 | 0.840 | 5 | 159315942 | 3 prime UTR variant | T/G | snv | 0.26 | 65 | ||
rs34933034 | 0.925 | 0.120 | 15 | 74787133 | intron variant | G/A;T | snv | 3 | |||
rs3761847 | 0.827 | 0.200 | 9 | 120927961 | intron variant | G/A | snv | 0.52 | 8 | ||
rs3761959 | 0.827 | 0.320 | 1 | 157699488 | intron variant | C/A;G;T | snv | 7 | |||
rs3890745 | 0.925 | 0.200 | 1 | 2622185 | intron variant | T/C | snv | 0.40 | 4 | ||
rs4409785 | 0.752 | 0.240 | 11 | 95578258 | intron variant | T/C | snv | 0.13 | 12 | ||
rs4750316 | 0.882 | 0.160 | 10 | 6351298 | non coding transcript exon variant | C/G;T | snv | 5 | |||
rs4810485 | 0.732 | 0.480 | 20 | 46119308 | intron variant | T/A;G | snv | 16 | |||
rs548234 | 0.763 | 0.360 | 6 | 106120159 | intron variant | C/T | snv | 0.76 | 11 | ||
rs57095329 | 0.677 | 0.480 | 5 | 160467840 | intron variant | A/G | snv | 7.8E-02 | 25 | ||
rs5844572 | 0.752 | 0.360 | 22 | 23893562 | intron variant | -/ATTC | delins | 11 | |||
rs6478109 | 0.752 | 0.320 | 9 | 114806486 | upstream gene variant | A/G | snv | 0.74 | 12 | ||
rs6679677 | 0.653 | 0.320 | 1 | 113761186 | upstream gene variant | C/A | snv | 6.7E-02 | 26 | ||
rs6822844 | 0.689 | 0.520 | 4 | 122588266 | regulatory region variant | G/T | snv | 0.10 | 20 | ||
rs6859219 | 0.925 | 0.160 | 5 | 56142753 | intron variant | C/A | snv | 0.20 | 4 |