Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs73036519 0.851 0.040 19 45245104 intron variant G/A;C snv 5
rs3138141 0.827 0.040 12 55721994 3 prime UTR variant C/A snv 0.19 0.16 5
rs11755724 0.807 0.320 6 7118757 intron variant A/G;T snv 5
rs11080055 0.851 0.040 17 28322698 intron variant A/C snv 0.54 5
rs10781182 0.851 0.040 9 74002804 intergenic variant T/G snv 0.54 4
rs114092250 0.851 0.040 5 35494346 intergenic variant G/A;T snv 4
rs142450006 0.851 0.040 20 45986353 regulatory region variant TTCT/-;TTCTTTCT delins 2.0E-02 4
rs148553336 0.851 0.040 1 196644043 intergenic variant T/C snv 7.7E-03 4
rs1626340 0.827 0.120 9 99161090 intergenic variant G/A;T snv 4
rs201459901 0.851 0.040 20 58078668 regulatory region variant -/A delins 0.21 4
rs61818925 0.851 0.040 1 196846320 upstream gene variant T/G snv 0.67 4
rs61941274 0.827 0.160 12 111694806 intron variant G/A;T snv 4
rs62247658 0.851 0.040 3 64729479 intron variant C/T snv 0.42 4
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 4
rs12357257 0.851 0.040 10 24710664 intron variant G/A snv 0.18 4
rs10490924 0.716 0.240 10 122454932 missense variant G/T snv 0.26 0.23 4
rs3750846 0.851 0.040 10 122456049 intron variant T/C snv 0.24 4
rs9564692 0.851 0.040 13 31247103 splice region variant C/T snv 0.40 0.36 4
rs147859257
C3
0.827 0.040 19 6718135 missense variant T/G snv 2.8E-03 2.4E-03 4
rs2230199
C3
0.763 0.240 19 6718376 missense variant G/C;T snv 0.15 4
rs1864163 0.882 0.120 16 56963321 intron variant G/A snv 0.26 4
rs2303790 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 4
rs5817082 0.851 0.040 16 56963437 intron variant -/A delins 4
rs641153 0.790 0.160 6 31946403 missense variant G/A;T snv 9.6E-02; 4.1E-06 4
rs121913059
CFH
0.716 0.280 1 196747245 missense variant C/T snv 1.4E-04 1.9E-04 4