Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs505922 0.724 0.357 None NA snp 0.37 24
rs8176704 0.923 0.071 None NA snp 6.2E-02 4
rs397507444 0.457 0.714 1 11794407 missense variant T/G snp 169
rs1805087
MTR
0.538 0.679 1 236885200 missense variant A/G snp 0.20 0.21 75
rs1800896 0.593 0.571 1 206773552 intergenic variant T/C snp 0.40 43
rs1137101 0.605 0.679 1 65592830 missense variant A/G snp 0.51 0.53 41
rs1800871 0.602 0.643 1 206773289 intergenic variant A/G snp 0.69 41
rs1800872 0.608 0.643 1 206773062 regulatory region variant T/G snp 0.69 37
rs1136410 0.622 0.357 1 226367601 missense variant A/G snp 0.21 0.16 35
rs5275 0.634 0.321 1 186673926 3 prime UTR variant A/G,T snp 0.40 29
rs2234922 0.652 0.321 1 225838705 missense variant A/G,T snp 0.19; 2.8E-05 0.23 28
rs20417 0.642 0.393 1 186681189 non coding transcript exon variant C/G,T snp 0.19 26
rs1137100 0.692 0.464 1 65570758 missense variant A/G snp 0.30 0.28 20
rs689466 0.685 0.321 1 186681619 regulatory region variant T/C snp 0.17 17
rs486907 0.715 0.286 1 182585422 missense variant C/T snp 0.31 0.30 16
rs1800947
CRP
0.734 0.250 1 159713648 splice region variant C/A,G,T snp 4.4E-05; 5.1E-02; 4.0E-06 3.2E-05; 5.0E-02 14
rs768623239 0.724 0.286 1 109689278 missense variant A/G snp 1.5E-05 14
rs1800890 0.724 0.250 1 206776020 intergenic variant A/T snp 0.32 13
rs763110 0.724 0.250 1 172658358 intergenic variant C/T snp 0.46 13
rs201765376
MTR
0.744 0.214 1 236838504 synonymous variant C/T snp 1.6E-05 3.2E-05 10
rs4245739 0.756 0.250 1 204549714 3 prime UTR variant C/A,G snp 0.77; 6.2E-06 0.78 9
rs74315364 0.784 0.143 1 182586014 stop gained C/A snp 3.6E-03; 4.0E-06 3.1E-03 8
rs2295080 0.801 0.214 1 11262571 regulatory region variant G/C,T snp 0.55 7
rs9350 0.801 0.143 1 241885372 missense variant C/T snp 0.21 0.19 7
rs1380576 0.821 0.107 1 204519150 intron variant G/C snp 0.60 5