Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs112735431 0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
rs2249825 0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs10754558 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs2305948
KDR
0.732 0.400 4 55113391 missense variant C/A;T snv 4.0E-06; 0.11 18
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18