Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 10
rs8065080 0.827 0.200 17 3577153 missense variant T/C snv 0.37 0.32 11
rs222747 0.827 0.240 17 3589906 missense variant C/A;G;T snv 0.72; 4.5E-06 8
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs5063 0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 12
rs11171739 0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49 10
rs1129844 0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05 13
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs1131498 0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22 13
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs2290400 0.790 0.360 17 39909987 intron variant T/C snv 0.48 9
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs10767664 0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs1800888 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs184003 0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs76863441 0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs696217 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46