Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs5029939 0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs121908117 0.708 0.440 3 48466707 missense variant G/A snv 17
rs1050501 0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15
rs2397084 0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs1143679 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs7848647 0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13
rs10488631 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 13
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs3810936 0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75 12
rs1270942 0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 11
rs3131379 0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 10
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9