Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs7080536 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 27
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs629301 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs2305948
KDR
0.732 0.400 4 55113391 missense variant C/A;T snv 4.0E-06; 0.11 18
rs6136 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 17
rs1803274 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 13
rs1410996
CFH
0.807 0.240 1 196727803 intron variant G/A snv 0.46 11
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 11
rs4151667 0.790 0.320 6 31946247 missense variant T/A snv 3.9E-02 3.4E-02 9
rs5128 0.925 0.080 11 116832924 3 prime UTR variant G/C snv 0.84 0.87 8
rs35457250 0.925 0.080 3 186620775 missense variant C/T snv 9.0E-03 8.1E-03 5
rs3789678
AGT
1.000 0.040 1 230713736 intron variant C/T snv 0.15 5
rs7950273 0.925 0.120 11 104160870 intron variant C/G snv 0.32 5