Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10118757 0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs1042031 0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 11
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs1044925 0.827 0.120 1 179354603 3 prime UTR variant C/A;G snv 6
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1048990 0.790 0.280 14 35292469 5 prime UTR variant C/G;T snv 0.19; 4.0E-06 8
rs1049255 0.776 0.320 16 88643329 3 prime UTR variant C/T snv 0.49 0.48 9
rs1051266 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1063537 0.807 0.320 3 186856286 3 prime UTR variant C/T snv 9.6E-02 6
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10754558 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10937273 0.882 0.160 3 186831906 downstream gene variant G/A snv 0.33 4
rs11053646 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs1122608 0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs1126643 0.807 0.160 5 53051539 synonymous variant C/T snv 0.39 0.36 6
rs112735431 0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs11536889 0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28