Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs763110 0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs10399805 0.851 0.240 1 203186870 upstream gene variant G/A;T snv 7
rs3790843 0.827 0.160 1 200041696 intron variant C/T snv 0.29 7
rs6691378 0.882 0.160 1 203187994 upstream gene variant G/A snv 0.19 6
rs438034 0.882 0.120 1 214657274 stop gained A/G;T snv 0.61 4
rs10754339 0.882 0.120 1 117147650 3 prime UTR variant G/A snv 0.88 0.76 3
rs11581557 1.000 0.080 1 39862786 intron variant A/C;T snv 1
rs371074389 0.732 0.320 2 136115226 synonymous variant C/T snv 4.0E-06 4.2E-05 16
rs766914563 0.732 0.320 2 136115082 synonymous variant C/T snv 7.0E-06 16
rs781172058 0.732 0.320 2 136115340 synonymous variant C/T snv 4.0E-06 16
rs11886868 0.752 0.280 2 60493111 intron variant C/T snv 0.65 12
rs1143633 0.752 0.280 2 112832890 intron variant C/G;T snv 11
rs4671393 0.790 0.400 2 60493816 intron variant A/C;G snv 11
rs966423 0.776 0.200 2 217445617 intron variant C/G;T snv 11
rs1143643 0.790 0.320 2 112830725 intron variant C/T snv 0.29 10
rs1143630 0.827 0.160 2 112834078 intron variant T/A;G snv 5
rs770327175 0.851 0.120 2 136115878 missense variant C/A;T snv 8.0E-06 5