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
CSK
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