Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs10911021 0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
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
rs12086634 0.827 0.280 1 209706914 intron variant T/G snv 0.21 0.20 6
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs16835198 0.882 0.200 1 32861080 downstream gene variant G/T snv 0.29 3
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1805094 0.716 0.440 1 65610269 missense variant G/C;T snv 0.16; 4.0E-06 16
rs1805096 0.827 0.200 1 65636574 synonymous variant G/A snv 0.46 0.43 6
rs2076349 0.882 0.120 1 209626885 missense variant C/T snv 0.13 0.13 3
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2274907 0.851 0.200 1 160882036 missense variant A/G;T snv 0.66 5
rs2568958 0.882 0.160 1 72299433 intron variant G/A;C snv 8
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs3480 0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs3737787 0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 11
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs5068 0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs5082 0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 8
rs5744168 0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 18
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs6688832 0.752 0.440 1 9263851 missense variant G/A;C snv 0.28; 1.2E-04 10