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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs486907 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 32
rs763110 0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs1800947
CRP
0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 28
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs1417938
CRP
0.776 0.320 1 159714396 intron variant T/A;C snv 0.28 10
rs4846048 0.752 0.280 1 11786195 3 prime UTR variant G/A snv 0.67 10
rs768873896 0.790 0.160 1 11794822 missense variant C/G;T snv 8.0E-06; 2.4E-05 7
rs2566 0.882 0.080 1 209615169 3 prime UTR variant G/A snv 0.27 6
rs55763075 0.827 0.120 1 11790377 3 prime UTR variant C/T snv 2.1E-05 6
rs10802996 0.882 0.080 1 241847325 upstream gene variant C/A;G snv 5
rs1048512 0.882 0.080 1 160025108 3 prime UTR variant G/A;T snv 0.13 3
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47