Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs11887534 0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs5219 0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs523349 0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 21
rs8192284 0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs1805094 0.716 0.440 1 65610269 missense variant G/C;T snv 0.16; 4.0E-06 16
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs2075291 0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs80356814 0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 15
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs773641005 0.742 0.240 16 58723829 missense variant T/C snv 14
rs1532085 0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs5068 0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs1337503417 0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 12
rs2230774 0.807 0.240 2 11218994 missense variant G/C;T snv 0.49 12
rs4918 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 12