Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs729302 0.827 0.160 7 128928906 intergenic variant A/C snv 0.28 6
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
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
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1057523354 0.763 0.480 13 110179387 missense variant C/A snv 13
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs367732974
F7
0.790 0.360 13 113105788 5 prime UTR variant G/A snv 8.9E-05 2.8E-05 9
rs549591993
F7
0.776 0.400 13 113105794 5 prime UTR variant C/A snv 4.0E-04 2.8E-05 12
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs37972 0.851 0.160 7 7967878 3 prime UTR variant T/A;C snv 5
rs2249825 0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26