Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs3804099 0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs11536889 0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs2249825 0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs12692386 0.827 0.160 2 9555777 5 prime UTR variant A/G snv 0.72 5
rs1524668 0.851 0.160 2 9557243 upstream gene variant A/C snv 0.64 4