Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs1044498 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs13333226 0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs10887800 0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs13447075 0.882 0.120 8 127998344 non coding transcript exon variant C/A snv 4
rs2648862 0.882 0.120 8 128049539 non coding transcript exon variant C/A snv 2.9E-02 4
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs8096658 0.925 0.120 18 79396537 intron variant C/G snv 0.39 5
rs12513649 0.851 0.160 5 173045049 regulatory region variant C/G;T snv 6
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11864909 0.851 0.160 16 20389517 intron variant C/T snv 0.23 7
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49