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
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
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
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
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
rs2855812 0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs7528684 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs1800451 0.776 0.240 10 52771466 missense variant C/T snv 3.2E-02 7.9E-02 9
rs6457374 0.851 0.200 6 31304484 intron variant C/T snv 0.81 9
rs13101828 0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs1042663 0.925 0.160 6 31937353 synonymous variant G/A snv 9.7E-02 0.12 3
rs8111 0.925 0.160 6 32115398 3 prime UTR variant C/T snv 0.26 3
rs9296009 0.925 0.160 6 32146738 downstream gene variant A/T snv 0.21 3
rs3132451 1.000 0.120 6 31614248 upstream gene variant G/C snv 0.18 2