Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1044925 0.827 0.120 1 179354603 3 prime UTR variant C/A;G snv 6
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs10754558 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12563308 0.925 0.080 1 62604040 missense variant T/A;C snv 1.9E-02 2
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs17114036 0.851 0.120 1 56497149 intron variant A/G snv 0.11 5
rs1748195 0.851 0.120 1 62583922 intron variant C/G;T snv 8
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4537545 0.790 0.160 1 154446403 intron variant C/T snv 0.48 11
rs464218 0.925 0.080 1 109313684 3 prime UTR variant G/A snv 0.43 2
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs505151 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55